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Clinical Research Jobs in New Brunswick, NJ

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Research Associate 5PY IQVIA RDS Inc.

Lake Hiawatha, NJ

$47,400–$169,300 / year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

30+ days ago

Executive Medical Director, Clinical Development - M.D. (Nephrology) Top Echelon

Jersey City, NJ

Quick Apply

The Clinical Development Executive Medical Director is the clinical leader of the specific clinical programs assigned with responsibility for outlining the overall clinical development strategy in line with regulatory requirements and sound scientific rationale, designing the clinical protocols, guiding the Clinical Operations team towards the adequate implementation of such protocols, ensuring adequate medical monitoring activities are implemented for the conduction of clinical studies and analyzing the data from the clinical program. The individual will also be responsible for ensuring adequate implementation of the global safety surveillance and pharmacovigilance for the investigational products, including review and analysis of safety data from clinical trials and other permitted sources (e.g., early access/expanded access programs, if applicable), identification and investigation of safety signals, and management of the benefit-risk profile for assigned compounds.

1 day ago

Clinical Nurse Educator - Emergency Department WhiteCap Search

East Orange, NJ

$97,000–$110,000 / year
Quick Apply

Ideal opportunity for an experienced ED educator, Nurse Educator, Clinical Nurse Specialist, or nurse leader seeking broader system-level impact while remaining clinically connected. Highly visible leadership role with direct influence on nursing practice, staff development, retention, quality outcomes, and patient safety.

30+ days ago

Clinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred * New York University School of Medicine

New York, NY

$70,481.60–$76,450 / year

Intermediate competency in medical terminology, and an advanced competency in Good Clinical Practice (GCP) guidelines, Federal Regulation that govern the conduct of human subjects research as well as Institutional Review Board and institutional policies and procedures related to human subjects research. Record, update, edit, and maintain confidential information relating to research biospecimens onto paperwork and/or web-based forms in a neat, accurate and timely manner and ensure subsequent data collection as required.

30+ days ago

Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials Mount Sinai Health System

New York, NY

$58,661–$81,675 / year

Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - 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. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" 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.

30+ days ago

Clinical Research Associate - Sponsor Dedicated IQVIA

Parsippany, Kansas

In this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.

19 days ago

Senior Clinical Research Associate (Field- Based) - Multiple Openings NAMSA Inc

$68,800–$133,700 / year

Assess the suitability of potential investigative sites through screening interviews, regulatory document review and evaluation of study information and provides input to the site selection process. Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc.

30+ days ago

Sr. Clinical Research Associate/Clinical trial Manager BridgeBio Pharma Inc

$145,000–$177,000 / year

Lead operational management for assigned regions and sites by driving site initiation activities, monitoring performance metrics, identifying and mitigating risks, driving escalations and action-item closure, and representing regional performance in study team and cross-functional discussions. Lead aspects of vendor management for the CRO and other key vendors (IRT, imaging, central and specialty labs, etc.), establishing expectations, ensuring deliverables are met, performance measures are maintained, and escalating as needed; address performance gaps and drive corrective actions to closure.

28 days ago

Clinical Research Associate - 170044 Zp Group Llc

$100,000–$140,000 / year

Partner with investigative sites and internal study teams to address findings, resolve issues, and maintain study timelines. Responsibilities: of the Clinical Research Associate (CRA): Conduct onsite and remote monitoring activities to evaluate study progress, participant safety, and protocol compliance.

30+ days ago

On-site Clinical Research Associate Protagonist Therapeutics

Newark, New Jersey

The Company also has a number of clinical and preclinical programs based on clinically and commercially validated targets and addressing unmet medical needs, including an oral IL-17 antagonist peptide, anti-obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin discovery programs. Clinical Research Associate About Us Protagonist Therapeutics is a biopharmaceutical company built on a proprietary peptide technology platform that has now produced two FDA-approved, first-in-class medicines, generating royalties and milestones from global commercial partnerships with Johnson and Johnson and Takeda Pharmaceutical Company Limited.

30+ days ago

Clinical Research Associate II - FSP Precision Medicine Group LLC

$91,500–$137,300 / year

Precision's uniquely integrated offerings enable the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for complex disease states. Essential functions of the job include but are not limited to: Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports.

3 days ago

Clinical Research Associate - Sponsor Dedicated IQVIA Holdings Inc

Parsippany, NJ

$74,500–$197,500 / year

19 days ago

Senior Clinical Director, Clinical Research, Hematology Merck & Co Inc

Rahway, NJ

$282,200–$444,200 / year

The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.

30+ days ago

Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic Worldwide Clinical Trials Holdings Inc

$97,000–$193,000 / year

To best support our sites, we're seeking candidates who are based in the Northeast and Mid-Atlantic region of the United States Travel will primarily be regional, with occasional travel to support sites in other locations as needed. Conduct all types of monitoring visits: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs),Interim Monitoring Visits (IMVs) and Closeout Visits (COVs).

30+ days ago

Senior Clinical Research Associate - CNS/Psychiatry - Northeast Worldwide Clinical Trials Holdings Inc

$97,000–$193,000 / year

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

30+ days ago

Clinical Research Pharmacist Adams Clinical

New York, NY

$100–$115 / hour

Monitor Visits: Meet with Clinical Research Associates (CRAs) during monitoring visits to review pharmacy binders, drug accountability records, and resolve queries. Investigational Product (IP) Preparation: Prepare, compound/reconstitute, and dispense IV infusions, subcutaneous injections, and oral medications in strict accordance with the study protocol and Pharmacy Manual.

9 days ago

Clinical Research Associate National Veterinary Associates

Remote

$80,000–$95,000 / year

This role serves as a strategic and operational lead for assigned studies, exercising discretion and independent judgment in planning trial activities, identifying and resolving site and study issues, prioritizing competing demands, and driving decisions that materially influence study timelines, site performance, sponsor satisfaction, data quality, and overall business results. The CRA acts as a primary liaison among sponsors, hospital teams, and internal stakeholders and is expected to operate with a high degree of autonomy in managing study conduct, recommending solutions, setting priorities, and shaping processes that support the successful delivery of Ethos Science services.

7 days ago

Senior Clinical Research Associate BeOne Medicines AG

$105,800–$140,800 / year

The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. General Description: The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

30+ days ago

Senior Clinical Research Associate Terumo Medical Corp

Somerset, NJ

$92,320–$126,940 / year

Support the investigator evaluation and recruitment process: o Create phone scripts, questionnaires, and other assessment tools for use in the selection of sites; o Assist team in the development of site recruitment and retention strategy; o Initiate contact with PIs, conduct pre-visits, assess potential investigators and recommend suitability of the site; Assist clinical team with study start-up activities: o Assist in development of protocol / ICF / CRF / CRF completion guidelines, preparation and maintenance of monitoring plans, study binders, study manuals, and other site specific and monitoring tools; o Requests and collects initial regulatory documentation; o Ensure that sites fulfill their regulatory obligations and submit study documents for IRB review and approval; o Performs study tracking and advises PM when an investigational site is approved and ready to receive investigational device supplies; Site Management and study execution activities: o Plan and conduct training / site initiation, interim and close-out visits. Thorough understanding of operational aspects of clinical research and regulatory regulations; Good interpersonal, problem solving and communication skills; Excellent follow-through capability; Self-motivated, attention to detail and organizational skill; Experience with various computer systems / applications and clinical trial management systems; willingness to learn new systems / databases as needed.

30+ days ago

Clinical Research Budget Manager, Office Of Research And Project Administration Memorial Sloan-Kettering Cancer Center

New York, NY

Remote

$83,800–$134,000 / year

Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. 2-4 years in clinical research financial management, including budget development, Medicare coverage analysis, clinical trial agreements, invoicing, and fiscal management.

14 days ago

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Clinical Research Jobs in New Brunswick, NJ

Research Associate 5PY IQVIA RDS Inc.

Executive Medical Director, Clinical Development - M.D. (Nephrology) Top Echelon

Clinical Nurse Educator - Emergency Department WhiteCap Search

Clinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred * New York University School of Medicine

Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials Mount Sinai Health System

Clinical Research Associate - Sponsor Dedicated IQVIA

Senior Clinical Research Associate (Field- Based) - Multiple Openings NAMSA Inc

Sr. Clinical Research Associate/Clinical trial Manager BridgeBio Pharma Inc

Clinical Research Associate - 170044 Zp Group Llc

On-site Clinical Research Associate Protagonist Therapeutics

Clinical Research Associate II - FSP Precision Medicine Group LLC

Clinical Research Associate - Sponsor Dedicated IQVIA Holdings Inc

Senior Clinical Director, Clinical Research, Hematology Merck & Co Inc

Senior Clinical Research Associate - CNS/Psychiatry - Northeast/MidAtlantic Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate - CNS/Psychiatry - Northeast Worldwide Clinical Trials Holdings Inc

Clinical Research Pharmacist Adams Clinical

Clinical Research Associate National Veterinary Associates

Senior Clinical Research Associate BeOne Medicines AG

Senior Clinical Research Associate Terumo Medical Corp

Clinical Research Budget Manager, Office Of Research And Project Administration Memorial Sloan-Kettering Cancer Center

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