medical research scientist

bioMerieux

<div>The Clinical Research Scientist (CRS) leads the execution of the clinical studies that make up the company&rsquo;s clinical evidence generation program. In this role, you will execute clinical studies and/or programs worldwide in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures.
The Clinical Research Scientist collaborates closely with cross-functional teams, including associate Clinical Research Scientists, Disease State Scientists, Biostatistics &amp; Data Management, Logistics, Medical Writers, Regional Medical Affairs teams and other stakeholders to generate impactful clinical evidence that supports the company&rsquo;s strategy. This role is crucial in maintaining our commitment to scientific excellence and patient-centric approaches within the competitive global healthcare landscape. 
This position can be located in either St. Louis, MO OR Salt Lake City, UT.
Primary Duties
Team and Cross Functional Leadership: 
a. Leads the study team in the execution of clinical studies to meet the Evidence Generation Plan from study synopsis to data lock and final study report 
b. Partner with internal stakeholders to lead the development, review, and finalization of clinical protocols to meet regulatory and scientific objectives 
c. Contribute to the development of the study synopsis 
d. Partner with key stakeholders to create and manage the study execution team 
e. Collaborate closely with cross-functional teams including Regulatory Affairs, Quality Assurance, Biostatistics, Program Management, external vendors, and contract research organizations (CROs) to ensure high-quality study conduct 
f. Mentor Associate Clinical Research Scientist(s) and provide guidance on clinical operations processes, study management and other study execution tasks
Study Planning, Strategy and Reporting: 
a. Develop and manage study budgets, timelines, enrollment strategies, and resourcing requirements to ensure study milestones are met 
b. Develop and manage all required plans including clinical study project plans, study execution plans, risk and risk mitigation plans, monitoring plan, and communication plans 
c. Contributes to or leads the development of abstracts/posters of study results in collaboration with study team 
d. Develop clinical study reports and/or contribute to the development of scientific publications
Study Management and Site Management: 
a. Manage all aspects of clinical trial operations including study start-up, site initiation, patient enrollment, monitoring, and study close-out for bioM&eacute;rieux initiated research studies and collaborative studies 
b. Track study progress and provide regular status reports to stakeholders 
c. Assure study metrics and budget are input to corporate systems 
d. Oversee site selection, feasibility, study startup, site activation, enrollment, and ongoing execution 
e. Oversee clinical monitoring and data integrity 
f. Update trial management systems, including timelines and budgets 
g. Perform on-site and remote site qualification visits, site initiation visits, interim monitoring visits and site close out visits as required 
h. Oversee clinical site activities, reference laboratories, CROs, and other external partners to ensure adherence and compliance with protocol timelines, budgets, study milestones and quality standards 
i. Manage and coordinate IRB/EC document creations and communications 
j. Manage clinical trial agreements for sites 
k. Manage study documentation and filing with electronic trial master file (eTMF) platforms
Regulatory Compliance: 
a. Follow Corporate (e.g., SOP&rsquo;s) and local/regional regulatory requirements 
b. Participate in the review and revision of Clinical Operations Standard Operating Procedures (SOPs) to assist Medical Affairs leadership with continuous process improvement initiatives
Quality and Compliance: 
a. Identify and mitigate risks throughout the clinical trial lifecycle 
b. Assure a quality plan is in place
Data Management: 
a. Oversee and manage electronic data capture (EDC) systems 
b. Oversee data collection activities, compliance, and inspection readiness 
c. Oversee electronic trial master file (eTMF) platforms to ensure data integrity and regulatory compliance
Communication: 
a. Lead internal and external study meetings with relevant stakeholders 
d. Organize and drive study meetings and other study activities as assigned 
e. Participate in core team meetings to provide clinical insights and contribute to strategic decision-making 
f. Outline and communicate safety issues and planned mitigations in collaboration with internal stakeholders
Vendor management: 
a. Negotiate contracts and budgets in partnership with the legal team 
b. Manage clinical trial agreements with external vendors 
c. Manage vendor performance according to contract
Perform all work in compliance with company quality procedures and standards.
Perform other duties as assigned.
Experience<ul><li>
Bachelor's Degree required in a scientific, medical, or healthcare discipline</li><li>
2+ years of professional related experience in clinical trial management, preferably in diagnostics or medical device required.</li><li>
Certifications including ACRP-CP or ACRP-PM a plus.
</li><li>Excellent knowledge of clinical trial processes, systems, and tools (e.g., CTMS, EDC, eTMF), with the ability to oversee quality, data integrity, and inspection readiness.
</li><li>Proven leadership and stakeholder-management capabilities, with the ability to influence without authority and build strong relationships across functions and with external partners.
</li><li>Experience negotiating clinical research contracts and budgets
</li><li>Knowledge of Good Clinical Practice ICH/GCP and other applicable regulations, fundamental knowledge of clinical research and monitoring requirements
</li><li>Experience managing all major aspects of strategic planning, organization, implementation, and delivery of clinical studies.
</li><li>Understanding the US and European Medical Testing environments and relevant professional societies and guidelines (e.g. FDA, CE-Mark IVD Directives, CAP, CLIA, WHO)
</li><li>Proven track record writing clinical study plans and study protocols
</li><li>Experience with the study budget oversight, risk mitigation, management of timelines, deliverables, and milestones
</li><li>Experience negotiating clinical research contracts and budgets with Investigators and sites
</li><li>Experience with electronic clinical trial systems and clinical data review
</li></ul>Knowledge, Skills, &amp; Abilities<ul><li>
Consistently upholds and reflects the core ethical principles and values that bioM&eacute;rieux promotes.</li><li>
Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives</li><li>
Effective Presentation Skills - including the ability to present technical data</li><li>
Solution oriented in the face of conflict</li><li>
Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently</li><li>
Managing and measuring work by tracking progress, performance, and goal achievement using metrics and KPIs.</li><li>
Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel
</li><li><ul><li>Advanced: demonstrates deep knowledge; manages complex tasks and integrates multiple tools independently</li></ul></li><li>
Functionally Required Knowledge, Skills, and Abilities
</li><li><ul><li>Ability to manage budget, timelines and multiple projects simultaneously</li><li>
Ability to learn new products and adjust to changing research directions</li></ul></li></ul><div>
The estimated salary range for this role is between $80,000 and $116,700. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux&rsquo;s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate&rsquo;s experience and will be presented in writing at the time of the offer.</div><div>
In addition, bioM&eacute;rieux offers a competitive Total Rewards package that may include:</div><ul><li>A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options</li><li>Company-Provided Life and Accidental Death Insurance</li><li>Short and Long-Term Disability Insurance</li><li>Retirement Plan including a generous non-discretionary employer contribution and employer match.</li><li>Adoption Assistance</li><li>Wellness Programs</li><li>Employee Assistance Program</li><li>Commuter Benefits</li><li>Various voluntary benefit offerings</li><li>Discount programs</li><li>Parental leaves</li></ul><div>
</div><div>
#LI-US</div></div>

Clinical Research Scientist

<div>
 We are looking for a
 
 Research Scientist
 
 to join our exceptional team at
 
 Schlumberger Doll Research (SDR)
 
 in Cambridge, Massachusetts&mdash;a place where pioneering science drives real‑world innovation.
 
 
 Schlumberger-Doll Research (SDR) conducts both fundamental and applied research to drive the development of innovative technologies for the Energy industry. Our teams are building the next generation of multi‑physics software and hardware systems designed to probe deeper and more accurately understand subsurface resources. This work leverages advanced data‑generating models, state‑of‑the‑art AI/ML algorithms, extensive domain expertise, and robust cloud computing infrastructure available within SDR and across SLB globally.
 
 
 As a Research Scientist, you will collaborate closely with scientists and subject‑matter experts to design and implement new computational and algorithmic models for next‑generation probing technologies. This includes working with advanced modeling tools and developing physics‑informed, data‑driven interpretation frameworks.
 
 
 Ideal candidates will bring a strong foundation in computational electromagnetics along with experience in areas such as machine learning, deep learning, signal processing, or statistical modeling and inference. A passion for tackling data‑intensive challenges in complex domain‑specific environments is essential. You&rsquo;ll draw insights from large databases and collaborate with experts spanning multiple specialties.
 
 
 We are looking for individuals who are driven, technically talented, and enthusiastic about scientific and technological innovation. Strong communication skills&mdash;both written and verbal&mdash;are important for thriving in SDR&rsquo;s multidisciplinary environment.
 
 
 <ul>
 <li>
 PhD in electrical engineering, computational physics, electromagnetics, or a related field with relevant domain specialization.
 </li>
 <li>
 Experience in computational modeling and familiarity with finite element analysis software (e.g., COMSOL, NGSolve, Ansys).
 </li>
 <li>
 Preferred (optional) skills: knowledge of inversion or optimization algorithms, AI/ML frameworks, and software development.
 
 
 
 </li>
 </ul>
 
 The compensation and benefits for this role are listed in compliance with applicable law. We are committed to offering fair and competitive pay aligned with each candidate&rsquo;s skills, experience, and qualifications, within the designated salary range for the role. Please note that the listed compensation and benefits apply only to successful candidates hired onto a local United States payroll.
 
 
 The anticipated annual salary range for this position is $105,280 - $213,800. SLB offers a comprehensive total rewards package, which includes variable pay, health care coverage, a retirement plan, protection programs, paid time off, and various training opportunities.
 
</div>

Research Scientist

Lumicity

<div>
 
 
 AI Research Scientist &ndash; NLP/Computational Linguistics
 
 
 
 
 
 
 A well-funded applied AI startup is building advanced systems to distinguish human-created content from machine-generated content. The team combines frontier research with real-world deployment, turning cutting-edge ideas into production systems used at scale.
 
 
 
 
 
 They&rsquo;re hiring an
 
 AI Research Scientist
 
 to improve and scale core detection models. This is a hands-on role where you&rsquo;ll train large neural networks, design experiments, and push model performance forward, while also shipping code into production.
 
 
 
 
 
 What You&rsquo;ll Do
 
 <ul>
 <li>
 Train and fine-tune large-scale deep learning models
 </li>
 <li>
 Design experiments to improve robustness and generalization
 </li>
 <li>
 Create and leverage synthetic data at scale
 </li>
 <li>
 Contribute new ideas that materially improve model accuracy
 </li>
 <li>
 Collaborate with engineering to deploy research into production systems
 </li>
 <li>
 Share insights through technical writing or publications where appropriate
 </li>
 </ul>
 
 
 
 
 This is not a purely academic role, you&rsquo;ll be expected to code, ship, and iterate.
 
 
 
 
 
 What They&rsquo;re Looking For
 
 <ul>
 <li>
 PhD in ML/AI/NLP (or equivalent research experience at a leading AI lab)
 </li>
 <li>
 Publications at top-tier venues (e.g., NeurIPS, ICML, ICLR, ACL, EMNLP)
 
 or
 
 meaningful contributions to deployed AI systems
 </li>
 <li>
 Strong understanding of generative models and modern LLMs
 </li>
 <li>
 Experience training models in PyTorch at scale
 </li>
 <li>
 Evidence your research has led to real-world impact
 </li>
 </ul>
 
 
 
 
 Bonus Points
 
 <ul>
 <li>
 Work in robustness, interpretability, synthetic data, or model evaluation
 </li>
 <li>
 Background in NLP, computational linguistics, vision, audio, or other adjacent ML domains
 </li>
 <li>
 Experience with distributed training or ML infrastructure
 </li>
 </ul>
 
 
 
 
 Ideal Profile
 
 <ul>
 <li>
 Early-career researcher (including strong new PhDs) who wants applied impact
 </li>
 <li>
 Industry researcher who wants more ownership and product exposure
 </li>
 <li>
 Someone motivated by AI integrity, trust, and responsible deployment
 </li>
 </ul>
 
 
 
 
 Small team. High ownership. Deep technical problems. Real-world impact.
 
</div>

Gencyte Therapeutics, Inc.

Gencyte Therapeutics, Inc. is an innovative life science startup developing next-generation CAR-T immunotherapy platforms for precision cancer treatment. We are seeking a highly motivated Scientist or Associate Scientist (In Vivo Research) to join our growing team. This position offers a unique opportunity to contribute directly to the development of cutting-edge adoptive cell therapies within a fast-paced, collaborative startup environment.Key Responsibilities<ul><li>Design, develop, and execute in vivo experimental protocols; generate clear, thorough scientific documentation and reports.</li><li>Establish, optimize, and execute murine models to evaluate novel adoptive T cell therapies in close collaboration with cross-functional teams.</li><li>Analyze, interpret, and effectively communicate experimental data through written reports and oral presentations.</li><li>Coordinate project activities and timelines to ensure alignment with research objectives and deliverables.</li><li>Supervise, train, and mentor research associates, as appropriate.</li><li>Manage multiple projects simultaneously while maintaining high scientific rigor, data integrity, and reproducibility.</li><li>Contribute to a collaborative, team-oriented culture within a dynamic startup environment.</li></ul>Required Qualifications<ul><li>Advanced degree (Ph.D., M.S., or B.S.) in molecular biology, cell biology, immunology, or a related discipline.</li><li>Minimum of 2 years of hands-on research experience; prior industry experience is strongly preferred.</li><li>Extensive experience designing, executing, and documenting in vivo studies, including preparation and management of IACUC protocols.</li><li>Demonstrated expertise in animal tumor models, including but not limited to:</li><li>Xenograft models (CDX and PDX)</li><li>Syngeneic models</li><li>Humanized mouse models</li><li>Strong proficiency with vivarium techniques, including:</li><li>Handling of mice and rats</li><li>Expertise in multiple dosing routes (IV, IP, SC, PO, IM, etc.)</li><li>Proficiency in blood collection methods (tail vein, retro-orbital, cardiac puncture)</li><li>Experience with tissue collection and necropsy</li><li>Strong data analysis and experimental interpretation skills.</li><li>Proven ability to work independently while contributing effectively within a team.</li><li>Strong organizational skills with the ability to manage competing priorities and timelines.</li></ul>Preferred Qualifications and Skills<ul><li>In-depth knowledge of pharmacology (PK/PD) and toxicology.</li><li>Experience with multicolor flow cytometry, immunophenotyping, and advanced cell culture techniques.</li><li>Prior experience in a fast-paced startup or early-stage biotech environment.</li><li>Demonstrated leadership experience, including mentoring or supervising junior scientists.</li><li>Strong commitment to scientific integrity and ethical research practices.</li><li>Exceptional attention to detail and data accuracy.</li><li>Adaptability to evolving project needs and comfort working under tight timelines.</li><li>Strong interpersonal and communication skills, with a constructive approach to collaboration and conflict resolution.</li><li>Highly self-motivated, creative, and goal-oriented.</li></ul>At Gencyte Therapeutics, you will be part of a passionate and driven team working to redefine cancer treatment through innovative immunotherapy platforms. If you are energized by challenging scientific problems and motivated to help translate groundbreaking research into transformative therapies, we encourage you to apply.Job Type: ContractPay: $30.00 - $50.00 per hourExperience:<ul><li>in vivo study: 2 years (Required)</li></ul>Ability to Commute:<ul><li>San Carlos, CA 94070 (Required)</li></ul>Work Location: In person

Scientist / Associate Scientist – In Vivo Research

Mount Sinai Health System

<div>Description
The Kimberly and Eric J. Waldman Department of Dermatology at the Icahn School of Medicine at Mount Sinai is dedicated to delivering superior, comprehensive dermatologic care that exceeds patient expectations, and to advancing the science of dermatology through research and education. 


From preparing the next generation of leaders, to providing cutting-edge and cost-effective treatment, the Department of Dermatology thrives on a passion to improve the lives of patients through science. 


The Research Scientist II is a senior-level laboratory or clinical research individual who conducts research involving the understanding of human diseases and the improvement of human health. S/he engages in clinical investigation or other research, production, technical writing, and related activities. The Research Scientist II make take the lead in the creation or participation of specific research projects. 
Responsibilities<ul><li>
Conducts research to develop methodologies, instrumentation and procedures for medical application, analyzing data and presenting findings.</li><li>
Assists in the design and conduct of complex clinical research studies requiring the determination and evaluation of alternative methods, computational modeling, diagnosis and treatment.</li><li>
Participates in studies to investigate human or animal disease, preventive methods, and treatments for disease.</li><li>
Follows strict safety procedures when handling materials to avoid contamination.</li><li>
May mentor students and less experienced research technicians.</li><li>
May confer with health departments, industry personnel, physicians, and others to develop health safety standards and public health improvement programs.</li><li>
Develops treatments and designs research tools and techniques.</li><li>
Explores subject area and defines scope and selection of problems for investigation through conceptually related studies.</li><li>
Develops hypotheses with senior colleagues to be tested and methodology for evaluating results.</li><li>
Examines the results of clinical trials and adjusts the dosage levels to reduce negative side effects or to induce better results.</li><li>
Develops new proposals for research and obtain support for new and/ or continuing research activities.</li><li>
Participates or leads the process in decision-making with potential impact on extensive scientific research activities.</li><li>
May present at relevant professional conferences.</li><li>
Other duties as assigned.</li></ul> 

Qualifications<ul><li>
Master&rsquo;s or Ph.D in Biological Science or related field is strongly preferred.</li><li>
3+ years minimum research experience (may include academic studies) with Masters; 5 years with a Bachelor&rsquo;s. Prior Faculty background preferred. Supervisory experience of lower-ranked research personnel is preferred.</li></ul> 

Employer Description
Strength through Unity and Inclusion

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.

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.

About the Mount Sinai Health System:

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.

Equal Opportunity Employer

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. 
Compensation
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 $87692 - $131538 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.</div>

Research Scientist II - Dermatology

The Alfred Foundation

<div>
 
 Bayside Health
 
 
 
 Bayside Health is a public health service delivering high-quality care across every stage of life for close to 1.2 million people living in metropolitan Melbourne, the Mornington Peninsula, Koo Wee Rup, Bass Coast and Southern Gippsland. We have more than 15 main sites, including hospitals, centres and clinics that provide comprehensive care from welcoming newborns to supporting older people and a full range of services in between. More than 22,000 dedicated staff are focused on providing exceptional, equitable, and locally connected care through shared expertise, compassion, and a commitment to continuous growth. Education and training are central to staff development as we encourage all employees to strive and thrive. Bayside Health was formed following the merger of Alfred Health, Bass Coast Health, Gippsland Southern Health Service, Kooweerup Regional Health Service and Peninsula Health on 1 January 2026.
 
 
 <ul>
 <li>
 12-month fixed term role with opportunity for renewal
 </li>
 <li>
 Full time (76 hours per fortnight)
 </li>
 <li>
 Level 2 Research Nurse Grade 3B (YU13) or Medical Scientist Grade 2 (RY4)
 </li>
 <li>
 Located at The Alfred
 </li>
 <li>
 Great staff benefits!
 
 
 </li>
 </ul>
 
 The Department
 
 
 
 The Medical Oncology Unit provides co-ordinated multidisciplinary management for adult patients with malignancies. An important component of this care is the Clinical Trial / Research activities we participate in, which enable us to offer forthcoming investigational treatments to our patients.
 
 
 Alfred Cancer Trials (ACT) conducts phase I, II and III trials, and is a participating member of both National and International Clinical Trials Groups, incorporating both pharmaceutical industry sponsored and investigator driven studies across a wide range of tumour types.
 
 
 
 The Role
 
 
 
 Trial coordination of allocated clinical trials within the framework of Good Clinical Practice.
 
 
 <ul>
 <li>
 Responsible for the delivery of clinical-trial-related care of patients
 </li>
 <li>
 Completing study related procedures and associated documentation
 </li>
 <li>
 Coordinate patient visits and scheduling as per trial requirements and available resources.
 </li>
 <li>
 Maintain good communication with study investigators
 </li>
 <li>
 Liaise with sponsors and clinical research organizations
 </li>
 <li>
 Report Adverse Events and Serious Adverse Events
 </li>
 <li>
 Educate patients and families about trials and patient safety
 </li>
 <li>
 Meet project deadlines and data locks with the direction and support of investigators and trial coordinators
 </li>
 <li>
 Collection of study data, data entry and maintenance of a study database
 </li>
 <li>
 Maintain accurate clinical records and associated clinical research data and site files
 
 
 </li>
 </ul>
 
 Essential
 
 
 
 
 Qualifications and Experience Required
 
 
 
 <ul>
 <li>
 Registered Nurse with the Nursing Midwifery Boad of Australia via AHPRA or Tertiary Medical Science qualification
 </li>
 <li>
 Current and satisfactory Police, and Working with Children checks
 </li>
 <li>
 Relevant post graduate education or progress
 </li>
 <li>
 Well-developed communication and interpersonal skills
 
 
 </li>
 </ul>
 
 Desirable
 
 
 
 <ul>
 <li>
 Basic understanding of oncology patients and their management
 </li>
 <li>
 Previous clinical trial experience
 </li>
 <li>
 Experience interacting with patients
 </li>
 <li>
 Current GCP certification
 </li>
 <li>
 Demonstrated ability to use clinical trial information systems (CTMS) and electronic case report forms (eCRF)
 </li>
 <li>
 Demonstrated knowledge of professional standards and knowledge of legal and ethical requirements in clinical trials
 
 
 </li>
 </ul>
 
 Staff Benefits
 
 
 
 <ul>
 <li>
 Salary packaging &amp; novated leasing through Maxxia
 </li>
 <li>
 Onsite car &amp; bike parking opportunities, deducted pre-tax!! *subject to availability
 </li>
 <li>
 Fantastic onsite fitness facilities at The Alfred through ProSport health and fitness
 </li>
 <li>
 Childcare services at The Alfred managed by KU Children&rsquo;s Services
 
 
 </li>
 </ul>
 
 If applicable, please specify specific requirements that you require in your cover letter or CV.
 
 
 
 
 For enquiries regarding this position, please contact Micheleine Uhe, Clinical Research Manager - m.uhe@alfred.org.au
 
 
 
 
 Applications close 11pm AEDT, Monday 30th March 2026.
 
 
 
 We embrace diversity and strive to have a workforce that reflects the communities we serve. We actively encourage applications from Aboriginal and Torres Strait Islander people, people with disability, and people of all genders, sexualities, and cultural backgrounds.
 
 
 If you require adjustments to the recruitment and selection process, or require an alternative format to any of the application materials, please don&rsquo;t hesitate to get in touch with the contact person listed on this ad.
 
 
 In accordance with the Health Services Amendment (Mandatory Vaccination of Healthcare Workers) Act 2020, health care workers in Category A or B roles (as determined by the department&rsquo;s risk ratings) are required to be vaccinated against influenza or hold an acceptable medical exemption.
</div>

Clinical Trial Coordinator

Metron Inc.

<div>
 
 Metron is an employee-owned company dedicated to delivering innovative solutions for the most challenging national security problems. For over 40 years, our principled approach to problem-solving has yielded creative solutions at the intersection of advanced mathematics, computer science, physics, and engineering. Our people are leaders in their technical fields and are passionate about solving challenging problems. We look for individuals who share this same passion and can apply their experience in real-world settings.&nbsp;&nbsp;
 
 
 &nbsp;
 
 
 Our Reston office is seeking a talented
 
 Signal and Information Processing Research Scientist
 
 to be part of a strong team of scientists, engineers, and operations experts in pursuit of applied research and development of effective and efficient solutions for real-world National Security System problems.
 
 
 The position responsibilities include data analysis, signal &amp; information processing, environmental (noise &amp; clutter) phenomenology identification/capture/modeling, and advanced algorithm development, implementation and testing. Initial projects will be related to undersea acoustic signal processing, and subsequent work may expand to include other signal processing methodologies.
 
 
 
 
 
 
 Required Qualifications:&nbsp;
 
 
 <ul>
 <li>
 Bachelor's degree in electrical engineering, physics, mathematics, or a related field.&nbsp;
 </li>
 <li>
 At least 2 years of relevant work experience.&nbsp;
 </li>
 <li>
 US Citizenship required; successful candidates will be subject to a security investigation and must meet eligibility requirements for access to classified information.&nbsp;
 </li>
 <li>
 Ability to research and implement advanced processing methods.&nbsp;
 </li>
 <li>
 Demonstrated knowledge, skills and abilities in sonar, radar, streaming video, SIGINT, or related sensing domain.&nbsp;
 </li>
 <li>
 Demonstrated knowledge, skills and abilities in statistical adaptive array and multichannel processing, stochastic processes and applications, classical inference/detection and estimation theory, fusion, tracking, classification, or related field.&nbsp;
 </li>
 <li>
 Ability to work in small groups, doing extended development with minimal oversight and direction.
 </li>
 </ul>
 
 
 
 
 
 Desired Qualifications&nbsp;
 
 
 <ul>
 <li>
 Active DoD security clearance.&nbsp;
 </li>
 <li>
 Advanced degree in electrical engineering, physics, mathematics, or a related field.&nbsp;
 </li>
 <li>
 Experience in mathematical/physical modeling, simulation, and performance analysis.&nbsp;
 </li>
 <li>
 Experience analyzing data on very large and diverse scales.&nbsp;
 </li>
 <li>
 Programming proficiency in Java or C/C++.&nbsp;
 </li>
 </ul>
 
 
 
 
 
 Position Location:&nbsp;
 
 Reston, VA&nbsp;&nbsp;
 
 
 
 
 
 
 Perks and Benefits:
 
 &nbsp;
 
 <ul>
 <li>
 Medical, Dental and Vision Insurance&nbsp;
 </li>
 <li>
 Accompanying FSA and HSA options&nbsp;
 </li>
 <li>
 Additional Voluntary Benefits&nbsp;&nbsp;
 </li>
 <li>
 Paid Time Off&nbsp;&nbsp;
 </li>
 <li>
 9 Observed Holidays and 2 Floating Holidays&nbsp;&nbsp;
 </li>
 <li>
 Paid Parental Leave&nbsp;&nbsp;
 </li>
 <li>
 Tuition Reimbursement&nbsp;
 </li>
 <li>
 Professional Development Reimbursement&nbsp;
 </li>
 <li>
 Annual Salary Reviews&nbsp;&nbsp;
 </li>
 <li>
 Profit Sharing&nbsp;&nbsp;
 </li>
 <li>
 401(k) Traditional and Roth Options&nbsp;&nbsp;
 </li>
 <li>
 Gym and Fitness Reimbursement&nbsp;&nbsp;
 </li>
 <li>
 Employee Assistance Program&nbsp;&nbsp;
 </li>
 <li>
 Employee Referral Program&nbsp;
 </li>
 </ul>
 
 &nbsp;
 
 
 
 Metron is an Equal&nbsp;Employment&nbsp;Opportunity (EEO) employer. It is the policy of the company to provide equal employment opportunities to all qualified applicants without regard to race, color, religious, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.
 
 
 <ul>
 <li>
 
 VEVRAA Federal Contractor
 
 &nbsp;
 </li>
 </ul>
</div>

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10000 medical research scientist jobs Near Me

Clinical Research Scientist

Research Scientist

Research Scientist

Scientist / Associate Scientist – In Vivo Research

Research Scientist II - Dermatology

Clinical Trial Coordinator

Research Scientist