research associate ii

Vantive

<div><p>Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients&mdash; that is what Vantive aspires to deliver.</p><p></p><p>
We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don&rsquo;t settle for the mediocre. Each of us is driven to help improve patients&rsquo; lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.</p><p></p><p>
Vantive: A New Company Built on Our Legacy<br>
<br>
Since last year, we have been on a journey to separate our Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.<br>
<br>
At Vantive, you will become part of a community of people who are focused, courageous and don&rsquo;t settle for the mediocre. Each of us are driven to help improve patients&rsquo; lives worldwide. Join us as we revolutionize kidney care and other vital organ support.</p><p></p><p>
Job Description</p><p></p><p><b>
Job Title &ndash;Research Associate II</b></p><p><b>
Location &ndash; Whitefield, Bangalore</b></p><p><b>
Shift &ndash; General</b></p><p></p><p><b>
 Job Responsibilities:</b></p><p></p><ul><li><p>
As Tech Lead or Change Owner, define, organize, plan and execute activities related to product design change and new product registration in compliance with current international/regional/national regulations with minimal support of senior colleagues or independently.</p></li><li><p>
Provide technical assessment for product changes related to design, labeling, raw material, manufacturing support, regulatory compliance, quality improvement and new registrations in collaboration with senior scientists</p></li><li><p>
Lead, and coordinate - including follow-ups as required with global stakeholders - of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs.</p></li><li><p>
Provide technical information, &amp;/or prepare reports based on internal or external data available to formulate response to authorities&rsquo; questions</p></li><li><p>
Propose options, work closely with stakeholders and develop action plan for problem-solving, product and process improvement</p></li><li><p>
Establish, maintain and update technical &amp; Design documentation according to Good Documentation Practices</p></li><li><p>
Participate in and at times lead multi-functional and international project team for effective collaboration and deliverables</p></li><li><p>
Demonstrate excellent internal and cross-functional communication and provide regular status update of activities to senior management &amp; stakeholder with some supervisions from direct manager and senior members of the organization.</p></li><li><p>
Draft technically accurate reports with in-depth analyses as required using statistics or other relevant tools and mentor/coach help junior members to create information that can go into such reports</p></li><li><p>
Lead, and conduct activities related to exploration of innovation concepts and technology platforms, demonstrate critical mindset and &ldquo;out-of-the-box&rdquo; thinking.
</p></li></ul><h1 class="jobSectionHeader"><b> Qualifications</b></h1><ul><li><p>
Master&rsquo;s in Chemistry or Pharmacy (or related disciplines) with minimum 4 years of relevant experience, or PhD in chemistry or Pharmacy (or related disciplines) with experience in Pharmaceutical product development and life cycle management, preferably sterile injectable/parenteral formulations.</p></li><li><p>
Demonstrated ability in clear and effective communication (written, oral) and presentation skills to global stakeholders</p></li><li><p>
Excellent stakeholder management (local and global)</p></li><li><p>
A proven track record of leading small size projects &ndash; especially Change Controls in Pharmaceutical industry</p></li><li><p>
Demonstrated ability to work in a matrix environment with multiple stakeholders</p></li><li><p>
A proven track record of effectiveness in a fast-paced environment working in global teams</p></li><li><p>
Proven ability to deliver results by owning &amp; being accountable for budget, timeline, and product/project deliverables</p></li></ul><p></p><p><b>
 Skills</b></p><ul><li><p>
Adequate orientation towards Renal PD therapies and products with time.</p></li><li><p>
Hand-on knowledge of product development stages and life cycle management: development, stability, clinical, registration, process/technology transfer, production, suppliers, customer service</p></li><li><p>
Hands-on knowledge of Design Control documentation and process</p></li><li><p>
Working knowledge / familiarity of international/regional/national regulations and standards</p></li><li><p>
Demonstrated project management experience where business acumen, prioritization and portfolio management skills were required</p></li><li><p>
Experience with Statistics and Six Sigma tools</p></li><li><p>
Ability to work fairly independently.</p></li><li><p>
Can effectively communicate with internal and external customers.</p></li><li><p>
Demonstrates flexibility and the ability to shift gears between projects comfortably.</p></li><li><p>
Fluency in English</p></li><li><p>
Solid computer skills: email, documentation, and collaboration tools: e.g., WebEx, Teams, Microsoft Office products, etc.</p></li></ul><p></p><h1 class="jobSectionHeader"><b>
Equal Employment Opportunity</b></h1><p></p><p>
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic</p><p></p><p><b>
Reasonable Accommodation</b></p><p></p><p>
Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link</p><p></p><p><b>
Recruitment Fraud Notice</b><br>
<br>
Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.</p></div>

Research Associate II

Laborie Medical Technologies

<div><div><b>We believe that great healthcare is an essential safeguard of human dignity.</b></div><div>
At Laborie, we know the work we do matters &ndash; it&rsquo;s what fuels our motivation and contributes to our success. If you&rsquo;re ready to make a positive impact in the lives of patients across the globe, we&rsquo;d like to meet you.</div><div><b>
</b></div><div>
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We&rsquo;re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of <b>Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.</b></div><div><b>
</b></div><div><b>
Who We&rsquo;re Looking For:</b></div><div><div>
The Clinical Research Associate II (CRA-II) will perform tasks related to supporting operational strategy and execution of clinical studies, supporting the strategy as defined in the Clinical Affairs Team. Provide support for essential daily clinical study activities, including Good Clinical Practice inspection readiness, following established protocols under the general management of the Clinical Program Manager or designee. Work with Clinical Research study teams, Clinical Research Organizations (CROs), and investigation sites to support clinical study activities as defined by the clinical trial operating model. Perform departmental tasks as needed.</div></div><div><b>
</b></div><div><b>
About the Role:</b></div><ul><li>
Assist with site selection, start-up activities overall study execution for study adherence.</li><li>
Conducts all aspects of study site management for clinical studies according to LABORIE Standard Operating Procedures (SOPs), ICH-GCP, MDR and local regulations and to ensure data are up to date per reporting metrics, query resolution, and data entry, including in the recruitment of potential investigators and sites.</li><li>
Develops and maintains strong working relationship with Investigators and study staff, serving as an ambassador to promote LABORIE high quality and ethical image</li><li>
Communicates effectively with site personnel, including the Principal Investigator (PI), to troubleshoot and provide appropriate solutions to study-related issues</li><li>
Supports site feasibility, identification, and selection activities.</li><li>
Maintains study tracking, in accordance with the demands of the study</li><li>
Supports completion of monitoring visits per study protocol, monitoring plan, and regulatory guidelines</li><li>
Serve as primary site contact and ensure proper handling of investigational products and other study supplies.</li><li>
Support planning and execution activities for study committee meetings (e.g., DMC, CEC, publication)</li><li>
Perform other tasks as directed</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor's degree in Life Sciences, medicine, or similar discipline.</li><li>
3-5 years&rsquo; experience in clinical research or equivalent experience gained with a CRO, pharmaceutical, or medical device company.</li><li>
Knowledge of ICH/GCP Guidelines, ISO 14155, and FDA and EU MDR, including a basic understanding of regulatory requirements in other countries.</li><li>
Ability to work with minimum supervision, excellent task management skills and collaboration, including verbal and written communication.</li><li>
Ability to travel (5-10%) domestically and internationally on an as-needed basis.</li><li>
Good verbal and written communication skills.</li><li>
Knowledge of MS Office and clinical trial management systems.</li></ul><div><b>
Why Laborie:</b></div><div>
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.</div><ul><li>
Paid time off and paid volunteer time</li><li>
Medical, Dental, Vision and Flexible Spending Account</li><li>
Health Savings Account with Company Funded Contributions</li><li>
401k Retirement Plan with Company Match</li><li>
Parental Leave and Adoption Services</li><li>
Health and Wellness Programs and Events</li><li>
Awarded 2024 Cigna Healthy Workforce Designation Gold Level</li></ul><p></p><div><i>
Laborie</i> <i>provides</i><i> </i><i>equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person&rsquo;s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual</i><i> </i><i>orientation,</i><i> </i><i>or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.</i></div><div>
</div><div>
#LI-Hybrid</div></div>

Clinical Research Associate II

Gladstone Institutes

<div><div>Category:</div>
Science<div><br>
Lab/Area:</div>
Theodoris Lab<div></div><div>
Description:</div><div></div><div>
Who we are:</div><div>
The Gladstone Institutes is a leading independent, not-for-profit research organization dedicated to improving human health through groundbreaking biomedical research and education. Our work spans neuroscience, cardiovascular biology, immunology, and stem cell biology, with a strong emphasis on understanding and treating disease. With approximately 600 team members, including world-renowned scientists and biomedical leaders, Gladstone fosters a collaborative and innovative environment. Located at the Mission Bay Campus in a state-of-the-art facility, we offer competitive salaries, comprehensive benefits, and the resources to empower individuals to maximize their potential and make a meaningful impact on global health.</div><div></div><div>
About the Role:</div><div>
The laboratory of Christina Theodoris, MD, PhD, is seeking a talented and motivated Research Associate (I, II, III, or Senior) with a background in experimental genomics to join the research program in the Gladstone Institute of Cardiovascular Disease and the Gladstone Institute of Data Science and Biotechnology.</div><div></div><div>
The Theodoris Lab focuses on leveraging cutting-edge experimental genomics and machine learning to map the gene networks driving cardiovascular disease and to develop network-correcting therapies. This is a unique opportunity to work at the interface of experimental and computational biology in a highly collaborative and interdisciplinary environment.</div><div></div><div>
What you will do:</div><ul><li><div>
Perform a variety of molecular biology and genomics experiments, including RNA/DNA purification, PCR, cloning, and sequencing library preparation.</div></li><li><div>
Conduct cell culture experiments, particularly with induced pluripotent stem cells (iPSCs).</div></li><li><div>
Contribute to single-cell and/or ChIP-seq experiments and analyses.</div></li><li><div>
Manage laboratory operations, including organization, ordering supplies, and maintaining compliance with safety protocols.</div></li><li><div>
Collaborate closely with computational biologists to integrate experimental and analytical approaches.</div></li><li><div>
Actively participate in lab meetings, present findings, and contribute to research discussions.</div></li><li><div>
Assist in the training and mentorship of junior lab members.</div></li></ul><div></div><div>
What you will need:</div><ul><li><div>
BS/BA and/or MS/MA in a related field (e.g., molecular biology, genomics, bioengineering, or a similar discipline).</div></li><li><div>
2+ years of related laboratory experience.</div></li><li><div>
Proficiency in tissue culture, especially with induced pluripotent stem cells (iPSCs).</div></li><li><div>
Hands-on experience with molecular biology techniques such as RNA/DNA purification, PCR, and cloning.</div></li><li><div>
Experience in experimental genomics, including sequencing library preparation (e.g., single-cell sequencing, ChIP-seq).</div></li><li><div>
Strong organizational skills, attention to detail, and the ability to work both independently and collaboratively.</div></li></ul><div></div><div>
What is preferred:</div><ul><li><div>
Prior experience in cardiovascular biology, stem cell differentiation, or gene regulation studies.</div></li><li><div>
Familiarity with bioinformatics tools or experience collaborating with computational researchers.</div></li><li><div>
A demonstrated track record of scientific initiative, including contributions to publications or research presentations.</div></li><li><div>
Interest in long-term professional growth within the lab, including potential leadership opportunities.</div></li></ul><div></div><div>
How to apply:</div><div>
Please include the following application materials with your submission:</div><ul><li><div>
Resume/Curriculum Vitae (CV)</div></li><li><div>
Cover Letter describing your research experience, relevant skills, and motivation for applying to this position</div></li><li><div>
Contact information for three professional references</div></li></ul><div>
Salary Range:</div><div>
RA I- $27-$31/hr.</div><div>
RA II- $68K-$80K</div><div>
RA III- $75K-$88K</div><div><br>
Gladstone Perks &amp; Benefits</div><ul><li><div><i>
People</i>&ndash;work with talented, committed, and supportive teammates within an organization that values each member of its community.</div></li><li><div><i>
A meaningful place to grow and learn</i>&ndash;whether it&rsquo;s your professional skills or scientific knowledge, we have the resources and environment to advance either so you can better support Gladstone&rsquo;s mission to drive a new era of discovery in disease-oriented science and to mentor tomorrow&rsquo;s leaders in an inspiring and excellent environment.</div></li><li><div><i>
Healthy work/life balance</i>&ndash;you are highly engaged and productive at work because you can have time to recharge and enjoy a vibrant life outside of work.</div></li><li><div><i>
Compensation</i>&ndash;competitive salary. Title and salary will be commensurate with education and experience.</div></li><li><div><i>
Excellent benefits</i>&ndash;generous medical, dental, vision, retirement plan, paid vacation, commuter benefits, access to free shuttle transportation.</div></li></ul><div><br>
Gladstone is committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, sex, religion, national origin, ancestry, age, marital status, medical condition, physical or mental disability, veteran status, sexual orientation, or any other non-job related characteristic. We make all employment decisions so as to further this principle of equal employment.</div></div>

Research Associate I / II or III

Syneos Health

<div><p><b>Description</b>
</p>CRA II | Sponsor Dedicated | Oncology (Home-Based - Buffalo, NY)<p></p><p>
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p><p>
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.</p><p></p><p>
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.</p><p></p><p>
Discover what our 29,000 employees, across 110 countries already know:</p><p></p><p><b>
WORK HERE MATTERS EVERYWHERE</b></p><p></p><p>
Why Syneos Health</p><ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul><p></p><p><b>
Job Responsibilities</b></p><p></p><ul><li>
Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.</li><li>
Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient&rsquo;s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.</li><li>
Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements.</li><li>
May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.</li><li>
Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.</li><li>
Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.</li><li>
For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets.</li><li>
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements</li><li>
Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.</li><li>
Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li><li>
Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Additional responsibilities include:Site support throughout the study lifecycle from site identification through close-out. Knowledge of local requirements for real world late phase study designs.Chart abstraction activities and data collection<br>
Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/Project Manager. Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations.</li></ul><p></p><p>
Qualifications:</p><ul><li>
Bachelor&rsquo;s degree or RN in a related field or equivalent combination of education, training and experience</li><li>
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li><li>
Must demonstrate good computer skills and be able to embrace new technologies</li><li>
Excellent communication, presentation and interpersonal skills</li><li>
Ability to manage required travel of up to 75% on a regular basis</li><li>
US ONLY: As part of your employment with Syneos Health, you may be deployed to Sites that require certain medical and other personal information to gain facility access. Pursuant to our Employee Privacy Notice, Syneos Health can provide the Sites with the information necessary for you to gain such access. Further, a Site may ask you for additional information beyond that which Syneos Health has in its possession. You are required to comply with any such Site requests as a condition of your employment with Syneos Health. Please note that failure to provide requested information may result in a Site barring you from entry, which could put your ongoing employment at risk.</li></ul><p></p><p>
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.</p><p></p><p>
Salary Range:</p>
$70,100.00 - $126,100.00<p></p><p>
The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate&rsquo;s qualifications, skills, competencies, and proficiency for the role.</p><p></p><p><b>
Get to know Syneos Health</b></p><p><br>
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.</p><p></p><p>
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.</p><p></p><p>
http://www.syneoshealth.com</p><p></p><p><b>
Additional Information</b></p><p><br>
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p><p><b>
Summary</b>
</p>Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Established and productive individual contributor. May manage defined components of projects or processes within area of responsibility. Requires practical knowledge of a professional area, typically obtained through education combined with experience.</div>

CRA II | Sponsor Dedicated | Oncology (Home-Based - Buffalo, NY)

ICON plc

<div>Site Specialist II, Study Start Up<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Site Specialist II (Study Start Up Associate II) to join our diverse and dynamic team. As a Site Specialist II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.</div><div></div><div>
What you will be doing</div><ul><li><div>
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.</div></li></ul><ul><li><div>
Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence</div></li></ul><ul><li><div>
Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.</div></li></ul><ul><li><div>
Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li></ul><ul><li><div>
Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.</div></li></ul><ul><li><div>
Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.</div></li></ul><ul><li><div>
Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Site Specialist II, Study Start Up

American Dental Companies

<div><p><b>Join Our Team as a Full-Time Dentist at Richard L. Powers II, D.D.S.!</b></p><p>
Richard L. Powers II, D.D.S. is seeking a talented full-time associate dentist to step into a high-producing role and serve our loyal and expanding patient base. This is a unique opportunity to join a PPO/FFS practice with <b>annual collections of $2.2 million </b>and a steady influx of<b> 70 new patients each month!</b></p><p><b>
Why Choose Richard L. Powers II, D.D.S.?</b></p><ul><li><b>Established Practice: </b>With <b>7,500 active patients,</b> our practice has a well-earned reputation for high-quality care and strong community ties.</li><li><b> High-Income Potential: Tearded compensation up to 40% of your collections</b></li><li><b>Growth Opportunity: </b>Partnership opportunity.</li></ul><p><b>
What We Offer:</b></p><ul><li>Competitive compensation package with achievable earning potential</li><li>State-of-the-art facilities with modern equipment</li><li>A robust patient base ensuring a busy schedule from day one</li><li>Opportunities for professional development and growth within the practice</li></ul><p><b>
Apply today!</b></p></div>

Associate Dentist - Powers Dentistry

Client of Garfield Robbins International

<div>
 <p>MAJOR UK / INT'L LAW FIRM - TOP-LEVEL INT'L FUNDS PRACTICE - £ATTRACTIVE (TAX FREE)<br>
Salary from £170,000 - £220,000 per annum + Bonus &amp; Benefits (Tax Free)<br>
This major UK and international law firm has an excellent opportunity for an ambitious Associate or Senior Associate to join their thriving and market leading UAE Private Funds practice in Dubai or Abu Dhabi. Their team advise a stellar list of major sponsors and institutional investors, incl. private equity houses, sovereign wealth funds, financial institutions and corporates, on big-ticket fund establishments and major investments into funds (including conventional and Shari a compliant structures). Their work often entails utilising funds in novel ways to diversify MENA region economies and create new opportunities, with fund types covering private equity, infrastructure, venture capital, real estate and technology; and domiciles spanning regional (DIFC, ADGM, UAE, Bahrain and Saudi), international and offshore (Cayman, Luxembourg, Channel Islands and Delaware). The scope of this top-level role will accordingly focus on the key areas of: (i) fund structuring and formation; (ii) investments into funds; and (ii) joint venture/co-sponsored/ fund-of-one  bespoke structures. The team are especially seeking an experienced individual who has strong knowledge of the ins and outs of limited partnership agreements, coupled with market knowledge of key negotiating points on major fund investments; ideally with experience of working with a range of different fund types and domiciles.</p></div>

Investment Funds Lawyer

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