director of preclinical research

HARBIN CLINIC

<div></div><div><div><div><div><div><div><div><div><p>NC, United States<br>
Job ID: R165905
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Shift: Various
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Job Type: Regular
</p></div><div><div><div><div>Share: mail</div></div></div></div><div></div><div><br>
</div></div><p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>Department:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>
38923 Wake Forest University Health Sciences - Gerontology<p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
Status:</b>
</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>Full time<p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
Benefits Eligible:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>
Yes<p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
Hou</b><b>rs Per Week:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>
40<p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
Schedule Details/Additional Information:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>
Varies<p></p><p><b>
Pay Range</b></p>
$0.00 - $0.00<p></p><p>
Wake Forest University School of Medicine invites applications to fill an open rank, tenure track position with an individual conducting translational research focused on the prevention and treatment of infection, healing and repair of bone, joints, and soft tissue management. The candidate will collaborate closely with national leaders in orthopaedic research, with particular interest in orthopaedic trauma, periprosthetic infection, and regenerative medicine. The Atrium Health Musculoskeletal Institute has strong clinical programs in musculoskeletal care, including orthopaedic surgery, primary care sports medicine, physical therapy. We are particularly interested in those working in the areas of:</p>
<ul><li>1. Surgical site and periprosthetic infection: prevention and treatment</li>
<li>2 Soft tissue management and healing (muscle, skin, wounds)</li>
<li>3. Bone and cartilage healing</li>
<li>4. Innovative treatments to promote healing</li>
</ul><p>Wake Forest University School of Medicine has a highly collaborative, research intensive faculty andoffers a dynamic environment for cutting edge multidisciplinary research. The rich collaborative environment includes many nationally recognized research entities including: theSticht Center for Healthy Aging and Alzheimer's Prevention, two NIA funded centers (Claude D. Pepper Older Americans Independence Center, Alzheimer's Disease Research Center), theDivision of Public Health Sciences, anNCI-funded Comprehensive Cancer Center, theWake Forest Institute for Regenerative Medicine (WFIRM), theCenter for Precision Medicine,and the WFU Primate facility which houses a breeding colony that includes aged animals.Additional information is available athttps://school.wakehealth.edu.</p>
<p><b>Applicant Qualifications:</b>Candidates should hold a PhD, MD or equivalent degree in a relevant field. In addition to growing and maintaining a robust, internationally recognized research program and working in a team science environment across the translational spectrum, successful candidates will be expected to contribute to teaching and mentoring of students/trainees and to support an inclusive culture that welcomes diversity of experience and thought. Start-up package, laboratory space, salary and rank will be commensurate with experience. Applicants will be appointed to the department best aligning with their program.</p>
<p><b>Applying:</b><i>Applicants should submit (1) a letter with statement of interest, (2) a complete curriculum vitae, and (3) a description of their current/future research program via the online application system. Application materials may also be emailed to Courtney Sola at </i><i>[email protected]</i></p>
<p><i>The Wake Forest University School of Medicine (WFUSM) is a U.S. News and World Report top 50 ranked medical school. WFUSMhas over $300M in annual, extramural funding that drives a cutting-edge Academic Learning Health System by integrating innovative research with excellent patient care across our enterprise.</i></p>
<p><i>The WFUSM serves as the academic core for Advocate Health &ndash; the 5th largest non-profit health system in the U.S. Our Enterpriseserves over 6 million patients with facilities in seven states across the Southeast and Midwest (AL, GA, IL, NC, SC, WS). Headquartered in Charlotte, NC, Advocate Health employs nearly 150,000 team members across 67 hospitals and over 1,000 care locations; offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs; and is committed to equitable care for all providing nearly $5 billion in annual community benefits.</i></p>
<p><i>Our highly integrated academic and clinical environment is deeply committed to improve health, elevate hope, and advance healing &ndash; for all. WFUSM is home to nationally- and internationally-recognized research in Alzheimer's Disease, Aging and Mobility, Cardiovascular Disease, Diabetes and Obesity, Cancer, Neurosciences, and Regenerative Medicine. Research excellence, coupled with a robust Informatics data infrastructure, clinically integrated implementation science efforts, and a firm commitment to the promotion of health equity renders the WFUSM a rich environment for breakthroughs in prevention, diagnosis, and treatment of disease and improvements in quality of life. We are in a phase of unprecedented growth and evolution, opening a second medical school campus in Charlotte, and recruiting over 40 new research-intensive faculty to bolster our commitment to growing our Academic Learning Health System.</i></p>
<p><i>***Advocate Health/Wake Forest University School of Medicine does not discriminate on the basis of race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, disability, or source of payment.</i></p>
<p><b><i>Culture Commitments</i></b></p>
<p><i>We create a space where all Belong</i></p>
<p><i>We Work as One to make great things happen</i></p>
<p><i>We earn Trust in all we do</i></p>
<p><i>We Innovate to better the now and create the future</i></p>
<p><i>We drive for Excellence &ndash; always</i></p>
<p><i>WFUSOM-1</i></p><p></p><p><b>
Our </b><b>Commitment to You:</b></p><p></p><p>
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more &ndash; so you can live fully at and away from work, including:</p><p></p><p><b>
Compensation</b></p><ul><li>
Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training</li><li>
Premium pay such as shift, on call, and more based on a teammate's job</li><li>
Incentive pay for select positions</li><li>
Opportunity for annual increases based on performance</li></ul><p></p><p><b>
Benefits and more</b></p><ul><li>
Paid Time Off programs</li><li>
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability</li><li>
Flexible Spending Accounts for eligible health care and dependent care expenses</li><li>
Family benefits such as adoption assistance and paid parental leave</li><li>
Defined contribution retirement plans with employer match and other financial wellness programs</li><li>
Educational Assistance Program</li></ul><p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
About Advocate Health</b></p><p></p><p>
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation&rsquo;s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p>
</p>Open Rank Tenure Track Position in Preclinical and Translational Musculoskeletal Research</div></div></div></div></div></div></div><div></div>

Open Rank Tenure Track Position in Preclinical and Translational Musculoskeletal Research

Stryker

<div><h3 class="jobSectionHeader"><b>Why join Stryker?</b></h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader"><b>
Job description</b></h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.<div><p>
Stryker is hiring a<b> Preclinical Specialist</b> for our <b>Neurovascular</b> division. This is an <b>onsite</b> role based in <b>Fremont, CA</b>.</p><p></p><p>
As the <b>Preclinical Specialist</b>, you will support the planning and execution of high-quality preclinical performance studies to assess the safety and effectiveness of Stryker Neurovascular devices. Working with guidance from the preclinical research team, you will assist with study logistics, data collection, and practical problem solving to help set up and troubleshoot test environments (in vitro, imaging, and lab setups) across product development and business continuity programs.</p><p></p><p><b>
What you will do</b></p><ul><li><p>
Maintain preclinical lab scheduling, maintenance, and readiness activities to help ensure a safe and organized working environment, including basic troubleshooting of equipment and test setups with guidance.</p></li><li><p>
Support onsite and offsite study activities by helping align schedules, confirming training status, and maintaining readiness and compliance requirements. Support the development, review, and execution of preclinical protocols under the direction of the preclinical research team, applying Stryker Neurovascular Quality principles.</p></li><li><p>
Support hands‑on product evaluation and in vitro modeling activities with R&amp;D and Marketing by following established procedures and communicating status to the preclinical team.</p></li><li><p>
Assist with assigned preclinical study tasks across New Product Development and Business Continuity projects, including data collection and accurate documentation, with guidance.</p></li><li><p>
Coordinate competitive product purchasing and help with consultant contracting and invoicing; provide cost inputs and status updates as requested.</p></li><li><p>
Develop skills to compile and summarize observations and data from preclinical studies by identifying test‑environment issues (test setups, equipment, lab/imaging conditions), and escalating questions with supporting data to the appropriate stakeholders to enable timely resolution.</p></li><li><p>
Develop skill in providing input on study model selection (animal, bench, cadaver) by gathering relevant information and sharing it with the preclinical researcher/core team.</p></li></ul><p></p><p><b>
What you need</b></p><p></p><p><b>
Required</b></p><ul><li><p>
High school diploma plus 6 years of relevant experience, or</p></li><li><p>
Associate degree plus 4 years of relevant experience, or</p></li><li><p>
Bachelor&rsquo;s degree in biomedical, science, or a healthcare‑related field.</p></li></ul><p></p><p><b>
Preferred</b></p><ul><li><p>
Technical aptitude and hands‑on laboratory operations experience.</p></li><li><p>
Ability to follow documented procedures, maintain training compliance, and produce accurate records with guidance.</p></li></ul><p></p><p><b>
Physical requirements</b></p><ul><li><p>
Medium work, including exerting up to 20 pounds of force.</p></li><li><p>
Ability to wear radiation protection clothing and stand for extended periods (up to ~8 hours/day as needed).</p></li><li><p>
Open to domestic and international travel (up to 30%) to support projects as needed.</p></li></ul><p></p><ul><li><b><br>
US30</b>: $94,300 - $157,200 USD Annual</li></ul></div><p></p>
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&amp;D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.</div>

Preclinical Specialist

Bristol Myers Squibb

<div>At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/
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This high-impact role sits at the intersection of commercial forecasting and market insights, supporting RayzeBio's enterprise decision-making across its full portfolio of radiopharmaceutical assets. This person will own short- and long-term commercial forecasting across RayzeBio's portfolio - including the launch forecast for RYZ 101 in GEP-NET - while also leading market research and analytics for RayzeBio's early-stage clinical and preclinical assets. The successful candidate will be a versatile, analytically rigorous, and commercially minded individual who can translate complex data into actionable insights for senior stakeholders.<br>
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Reporting to the Head of Data, Analytics and Insights, this person will serve as RayzeBio's primary owner of commercial forecasting and early-stage market insights. The forecasting remit spans the full portfolio - from near-term launch planning for RYZ 101 to long-range valuations for clinical and preclinical programs - and directly supports decision-making across Finance, Manufacturing, Business Development, Commercial, and Medical Affairs. On the insights side, this person will design and execute market research and analytics that help RayzeBio understand the potential of its emerging pipeline.<br>
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<b>Job Responsibilities</b><ul><li>
Commercial Forecasting</li><li>
Own short-range and long-range commercial forecasts across RayzeBio's full portfolio of assets, including RYZ 101, early-stage clinical and preclinical programs</li><li>
Own the launch forecast for RYZ 101 in GEP-NET, including patient flow modeling, epidemiology-based sizing and assumption documentation</li><li>
Integrate insights from market research, competitive intelligence, and real-world data to inform forecast assumptions</li><li>
Partner with finance, manufacturing, business development, commercial, and others to ensure forecasts are aligned with enterprise planning processes, including LTFP cycles, supply and demand planning, and portfolio valuation updates</li><li>
Prepare and deliver clear, insight-driven forecast updates to senior leadership and cross-functional stakeholders; proactively address questions on key assumptions and scenarios</li><li>
Build consensus among cross-functional teams around underlying forecast assumptions, and clearly communicate range of outcomes and key risks/opportunities</li><li>
Develop scenario analyses to support business development evaluations, pipeline prioritization decisions, and clinical development planning</li><li>
Market Research &amp; Insights</li><li>
Apply AI to improve team execution and decision-making</li><li>
Design and execute a primary market research program to support strategic planning for early-stage clinical and preclinical assets</li><li>
Conduct claims data analyses to generate insights on patient journeys, treatment patterns, disease epidemiology, and competitive dynamics</li><li>
Leverage and analyze standard syndicated data sets (e.g., IQVIA, Symphony Health) to monitor market trends and inform commercial strategy</li><li>
Synthesize findings from competitive intelligence activities across RayzeBio's portfolio, converting external signals into actionable strategic implications for internal stakeholders</li><li>
Collaborate with Medical Affairs, Clinical Development, and Commercial to integrate scientific and commercial insights into a unified view of each asset's opportunity</li><li>
Manage market research and analytics vendors to ensure quality, compliance, and timely execution of projects</li></ul><b>
Required Qualifications</b><ul><li>
Bachelor's degree in Business, Life Sciences, Statistics, or similar</li><li>
7+ years in pharma / biotech market research, analytics and / or consulting</li><li>
Demonstrated experience building and maintaining commercial forecasts, including patient-flow models and epidemiology-based approaches</li><li>
Direct experience designing and executing primary market research studies (quantitative and qualitative)</li><li>
Working knowledge of third-party data sources, including patient-level claims data and syndicated sales data</li><li>
Strong communication and storytelling skills, with a proven ability to translate complex analyses into clear, actionable recommendations for senior stakeholders</li></ul><b>
Preferred Qualifications</b><ul><li>
Advanced degree in Business, Life Sciences, Statistics, or similar</li><li>
Oncology or rare disease experience, strong preference for prior experience in radiopharmaceuticals</li><li>
Hands-on analytics experience (SQL, R, Python)</li><li>
Prior experience supporting a commercial launch</li><li>
Familiarity with business development support, including pipeline valuations and scenario modeling</li><li>
Experience supporting both US and ex-US (worldwide) commercial forecasting</li></ul><b>
Travel Required</b><ul><li>
25% as required</li></ul>
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
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<b>Compensation Overview:</b><br>
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San Diego - RayzeBio - CA: $182,753 - $221,454<br>
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The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
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Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
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Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</li><li>
<b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul><b>Work-life benefits include:
</b><br>
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Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
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All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.<br>
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<ul><li><b>Eligibility Disclosure: </b>T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul><br>
<b>RayzeBio and Bristol Myers Squibb</b><br>
<br>
RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.<br>
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<b>Supporting People with Disabilities</b><br>
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BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.<br>
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<b>Candidate Rights</b><br>
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BMS and RayzeBio will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.<br>
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If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
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<b>Data Protection</b><br>
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We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection/
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Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<br>
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If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response.
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R1601283 : Associate Director, Worldwide Forecasting and Insights</div>

Associate Director, Worldwide Forecasting and Insights

Marc

<div><p>MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.</p><p></p><p>
MARC is looking to have an experienced candidate for <b>Local Purchasing Specialist</b></p><p></p><ul><li><b>
Key responsibilities:</b></li><li><ul><li>
Review requisition requests, prepare purchase orders, and follow up on delivery</li><li>
Prepare price comparisons to ensure alignment with contract terms</li><li>
Negotiate and administer contracts with suppliers and vendors</li><li>
Analyze financial data, proposals, and reports to determine reasonable pricing</li><li>
Balance cost and quality to procure goods in the right quantity and value</li><li>
Evaluate suppliers/products and ensure compliance with laws, regulations, and company policies</li></ul></li></ul><br>
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Requirements</b><br>
<ul><li>
Bachelor&rsquo;s degree in business administration/commerce or equivalent with 0-2 years of experience</li><li>
Excellent command of English (written and spoken)</li><li>
Strong negotiation and communication skills</li><li>
Ability to analyze financial data and compare pricing effectively</li><li>
Detail-oriented with knowledge of purchasing policies and compliance standards</li><li>
Knowledge of Oracle ERP is a plus</li></ul></div>

Local Purchasing Specialist

King Abdullah University of Science and Technology

<p><b>Department/Division</b>: Research Translation Hub</p><p><b>Job Title</b>: Research Translation Engineer - Biotechnology</p><p><b>Reports to</b>: Manager, Research Translation</p><p><b>Position Summary</b></p><p>Reporting to the manager of research translation, the Biotechnology Research Translation Engineer will provide technical support and research translation guidance to KAUST researchers across a broad range of projects focused on preclinical drug discovery, assay development and biotech for food and agriculture. The job holder will contribute to the early-stage development and deployment of advanced technologies spanning vaccine development, in-vitro assays, NGS workflows, plant genetics and CRISPR plant editing. This role requires working collaboratively alongside researchers, technologists, and industrial partners to convert scientific innovations into functional systems. Activities span early‑stage research translation, technology scale‑up, field deployment, pilot‑unit engineering, technical assessments, and system performance optimization.</p><p><b>Major Responsibilities</b></p><p>&middot; Lead and provide technical support for drug discovery, vaccine development and gene editing research translation projects.</p><p>&middot; Design and optimize cell-based assays, optimize genomic library preparation, and validate experimental protocols for translation into commercial or clinical applications.</p><p>&middot; Convert research concepts into Target Product Profiles / Intended Use statements, user needs, and product requirements.</p><p>&middot; Run TRL assessments, gap analyses, and maturation roadmaps for biotech/genomics platforms.</p><p>&middot; Manage vendor engagements (CROs, sequencing providers): SOWs, timelines, QC and acceptance criteria.</p><p>&middot; Establish project governance: milestones, risk register, reporting cadence, and stakeholder alignment.</p><p>&middot; Collect and document feedback and identify necessary metrics to measure and optimize various product parameters against functional requirements</p><p>&middot; Contribute to project planning, cost estimation, and technical feasibility studies; track milestones and communicate progress to project leads and stakeholders.</p><p>&middot; Participate in project reviews, risk assessment and management</p><p><b>Personal Requirements:</b></p><p><b>Competencies</b></p><p>&middot; Experience translating biology into screening cascades for preclinical discovery.</p><p>&middot; Deep understanding of cell biology techniques, biological assay development, and modern genomics workflows.</p><p>&middot; Understanding of microbial or plant biotechnology workflows (strain engineering, functional genomics, CRISPR plant editing, crop improvement, plant assays, or transformation strategies).</p><p>&middot; Knowledge of vaccine development, diagnostic assay design and multi-omics analysis.</p><p>&middot; Knowledge of the research and development value chain, including technology readiness assessment.</p><p>&middot; Knowledge of intellectual property implications for scientific research projects.</p><p>&middot; Strategic planning, organization, time management, analytical, and critical thinking skills with the ability to identify and solve problems, make decisions, and implement changes.</p><p>&middot; Demonstrated ability to analyze workflows in order to streamline and improve business processes and workflows</p><p>&middot; Ability to work independently using own initiative, handle multiple and complex tasks and prioritize ongoing and new work assignments and deliver high-quality work against tight deadlines.</p><p>&middot; Strong analytical, communication, and documentation skills.</p><p>&middot; Ability to work across multiple projects and interdisciplinary teams.</p><p>&middot; Experience preparing technical reports, reviewing grant proposals, or regulatory submissions.</p><p><b>Qualifications</b></p><p>&middot; A degree in Cell Biology, Genetics, Molecular Biology, Bioengineering, or a highly related field.</p><p><b>Experience</b></p><p>&middot; 6 to 10 years of industry experience.</p><p>&middot; Demonstrated delivery of validated assays or workflows for high throughput screening, gene editing or similar application.</p><p>&middot; Extensive hands-on experience in molecular biology, next-generation sequencing (NGS) technologies, and cell culture optimization.</p><p>&middot; Experience with material &amp; test specs generation, protocol &amp; report writing, process &amp; test development, design verification, and validation.</p><p>&middot; Familiarity with quality systems (GLP/GMP) and regulated laboratory practices; experience interfacing with CLIA/CAP labs is a plus.</p><p>&middot; Experience in supporting technical (R&amp;D) teams to ensure timely delivery of biological innovations.</p><p>&middot; Knowledge of technology readiness levels, prototyping methodologies, and translational</p><p>research pathways.</p><p>Work Location: In person</p>

Research Translation Engineer - Biotechnology

Mount Sinai Health System

<div><b>Description</b><div>
The Clinical Research Program Director will lead the operational, regulatory, financial, and strategic coordination of a clinical and translational immunology research portfolio focused on the development and clinical implementation of cellular therapies for non-oncologic diseases.</div><div>
This role bridges basic science, translational research, and clinical trials, with a strong emphasis on regulatory execution, including IND submissions to the FDA for both drug and cellular therapy products.</div><div></div><div><br>
The ideal candidate brings deep experience in academic clinical research environments, IND-enabling activities, and early-phase clinical trials, and is comfortable managing complex, multi-stakeholder programs involving investigators, regulatory bodies, and institutional committees.</div><div></div><div><b><br>
Why Join Us</b></div><div>
This is a unique opportunity to help build and scale a cutting-edge translational immunology program advancing cellular therapies beyond oncology into new therapeutic areas. The Clinical Research Program Director will organize a hub-and-spoke model, within the Lipschultz Precision Immunology Institute at Icahn School of Medicine (PrIISM) serving as the central coordinating hub and clinical departments/divisions functioning as disease-specific spokes.</div><b>
Responsibilities</b><div><b>
Program &amp; Portfolio Management</b></div><ul><li>
Oversee day-to-day management of translational research programs in immunology and cellular therapy</li><li>
Coordinate cross-functional teams including faculty, clinical research staff, GMP facilities, regulatory affairs, and external collaborators</li><li>
Develop and manage project timelines, milestones, budgets, and deliverables across preclinical and clinical phases</li><li>
Track progress of multiple concurrent studies and ensure alignment with institutional and sponsor priorities</li></ul><div><b>
Clinical Trials &amp; Translational Research</b></div><ul><li>
Support design, startup, and execution of early-phase (Phase I/II) clinical trials involving cellular therapies for non-cancer indications</li><li>
Coordinate activities spanning pre-clinical development, IND-enabling studies, and clinical implementation</li><li>
Interface with clinical operations teams to ensure protocol adherence, subject safety, and data compliance/ integrity</li></ul><div><b>
Regulatory Strategy &amp; IND Submissions</b></div><ul><li>
Lead preparation, coordination, and submission of Investigational New Drug (IND) applications to the FDA, including for cell and gene therapy products</li><li>
Manage regulatory documentation (e.g., protocols, investigator brochures, CMC sections, pharmacology/toxicology data)</li><li>
Serve as liaison with FDA and support responses to information requests, clinical holds, and annual reports</li><li>
Ensure compliance with GCP, GMP, and applicable regulatory requirements</li></ul><div><b>
Operational &amp; Institutional Navigation</b></div><ul><li>
Guide studies through internal review processes (e.g., IRB, biosafety, data use, and institutional committees)</li><li>
Coordinate with technology transfer, legal, and compliance offices as needed</li><li>
Establish and refine workflows to streamline translational research operations within the department</li></ul><div><b>
Collaboration &amp; Communication</b></div><ul><li>
Serve as a central point of coordination between investigators, institutional leadership, sponsors, and external partners</li><li>
Prepare reports, presentations, and updates for internal stakeholders and funding agencies</li><li>
Facilitate multidisciplinary meetings and ensure clear communication across teams</li><li>
Performs other related duties.</li></ul><b>
Qualifications</b><ul><li>
Bachelor&rsquo;s degree required. Master&rsquo;s degree in life sciences, public health, regulatory science, or a related field strongly preferred. Advanced clinical or doctoral degrees (PhD, MD, RN, or equivalent) are also strongly preferred.</li><li>
Minimum of 7 years of experience in a hospital or medical environment, preferably within human subjects or clinical trials research, including at least 3 years of supervisory experience.</li><li>
Demonstrated experience managing clinical trials, particularly early-phase or investigator-initiated studies</li><li>
Direct experience preparing and submitting IND applications to the FDA, including cellular therapy and/or biologic products</li><li><p>
Experience in translational medicine, ideally in immunology or cell therapy (non-oncology focus preferred)</p></li></ul><p></p><div><b><br>
Skills &amp; Knowledge</b></div><ul><li>
Strong understanding of FDA regulatory pathways, especially IND requirements for drugs and cell-based therapies</li><li>
Familiarity with GCP, GMP, and IND-enabling preclinical requirements</li><li>
Proven ability to manage complex, multidisciplinary programs and timelines</li><li>
Excellent organizational, communication, and stakeholder management skills</li><li><p>
Ability to navigate academic institutional processes and regulatory committees</p></li></ul><p></p><b><br>
Employer Description</b><p><b>
Strength through Unity and Inclusion</b></p><br>
<p>
The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai&rsquo;s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual.</p><br>
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At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history.</p><br>
<p><b>
About the Mount Sinai Health System:</b></p><br>
<p>
Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time &mdash; discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients&rsquo; medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News &amp; World Report's Best Hospitals, receiving high &quot;Honor Roll&quot; status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News &amp; World Report&rsquo;s &ldquo;Best Children&rsquo;s Hospitals&rdquo; ranks Mount Sinai Kravis Children's Hospital among the country&rsquo;s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek&rsquo;s &ldquo;The World&rsquo;s Best Smart Hospitals&rdquo; ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally.</p><br>
<p><b>
Equal Opportunity Employer</b></p><br>
<p>
The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.</p><br>
<p><b>
Compensation</b></p><p>
The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $115494 - $194020.12 Annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.</p></div>

Clinical Research Program Director in Cellular Therapy and Biologics for Non-Oncology Diseases (Immunology and Immunotherapy)

Children's Hospital of Philadelphia

<div><p>SHIFT:</p>
Day (United States of America)<p></p><p><b>
Seeking Breakthrough Makers</b><br>
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Children&rsquo;s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.<br>
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At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care&mdash;and your career.<br>
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CHOP does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means.<br>
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<b>A Brief Overview</b><br>
A Clinical Research Coordinator position is open in the Center for Childhood Cancer Research (CCCR) at the Children&rsquo;s Hospital of Philadelphia (CHOP) and the University of Pennsylvania (UPENN). This position is part of Center for Precision Medicine for High-Risk Pediatric Cancer&rsquo;s biobanking operation.
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The goal is to bank clinically annotated frozen and viable patient specimen to support ongoing research efforts into understanding childhood cancer and to develop new therapeutic approaches. Supported projects include immunotherapy and targeted therapy preclinical studies, organoid and PDX models, and
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sophisticated molecular analysis of primary patient material.<br>
</p><p>The candidate will be a member of the Precision Medicine for High-Risk Pediatric Cancer Team and will be primarily responsible for interfacing with clinical and pathology teams for the collection of blood, bone marrow and tumor material, and processing viable blood and tumor material. In addition, the candidate will partner with another clinical research coordinator to consent patients and for data entry. In addition, the candidate may have some involvement with PDX (patient derived xenograft) models. All these duties will require an individual who is willing to work with patients, patient samples as well as mouse tumor
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models. Ideal candidates will have great communication skills and meticulous attention to detail.
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<b>What you will do</b></p><ul><li>
Core responsibilities</li><li>
Adhere to an IRB approved protocol</li><li>
Participate in the informed consent process of study subjects</li><li>
Support the safety of clinical research patients/research participants</li><li>
Coordinate protocol related research procedures, study visits, and follow-up care</li><li>
Screen, recruit and enroll patients/research participants</li><li>
Maintain study source documents</li><li>
Under the supervision of PI Report adverse events</li><li>
Understand good clinical practice (GCP) and regulatory compliance</li><li>
Educate subjects and family on protocol, study intervention, etc.</li><li>
Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, and with HIPAA and management of confidential materials</li><li>
Must comply with federal, state, and sponsor policies</li><li>
For multi-site studies or collaborations, support communication and meeting scheduling across teams</li><li>
Related responsibilities</li><li>
Manage essential regulatory documents</li><li>
Register study on ClinicalTrials.gov as appropriate</li><li>
Complete case report forms (paper &amp; electronic data capture) and address queries</li><li>
Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie,DSMB, independent safety officer)</li><li>
Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate</li><li>
Facilitate study close out activities as appropriate</li><li>
Coordinate research/project team meetings</li><li>
Collect, process and ship samples as applicable to the protocol</li><li>
Schedule subject visits and procedures</li><li>
Retain records/archive documents after study close out</li></ul><p><b>
Education Qualifications</b></p><ul><li>
High School Diploma / GED Required</li><li>
Bachelor's Degree Preferred</li></ul><p><b>
Experience Qualifications</b></p><ul><li>
At least two (2) years of clinical or research related experience Required</li><li>
At least three (3) years of clinical or research related experience Preferred</li></ul><p><b>
Skills and Abilities</b></p><ul><li>
Basic knowledge of IRB and human subject protection</li><li>
Strong verbal and written communications skills</li><li>
Strong time management skills</li><li>
Ability to collaborate with stakeholders at all levels</li></ul><p><b><br>
To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. </b><b>Learn more.</b><br>
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<b>EEO / VEVRAA Federal Contractor</b><b> | </b><b>Tobacco Statement
</b></p><p></p><p><b>SALARY RANGE:</b></p><p></p>
$51,730.00 - $64,660.00 Annually<p></p><p>
Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.</p><p></p><p>
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At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.</p></div>

Biospecimen Clinical Research Coordinator I - Precision Medicine

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