- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Global Associate Director, will lead projects and contribute to the payer evidence strategy for key ... a Global remit. The role requires a strong technical background in evaluating clinical data and leading HEOR analyses such as systematic literature reviews, indirect… more
- Actalent (New York, NY)
- The Clinical Trial Associate (CTA) will play a vital role in supporting clinical studies and the Clinical Operations Department. This includes ... managing various administrative tasks and providing assistance to Clinical Project Managers. Responsibilities + Generate agendas and minutes, maintain study… more
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is accountable for… more
- Pfizer (New York, NY)
- …in mechanistic PK/PD modeling/systems pharmacology, literature meta-analyses, population modeling, and clinical trial simulations using NONMEM, R, etc.). + ... **OVERVIEW:** Exciting opportunity in Clinical Pharmacology! Our Clinical Pharmacology Team is looking for an Associate... Clinical Pharmacology Team is looking for an Associate Director to support the exciting portfolio in Internal… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents ... The Associate Director, Clinical Sciences contributes to the development, evaluation, planning and execution of Internal Medicine clinical studies and… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- Touro University (Hawthorne, NY)
- Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities + Assist in new IRB… more
- Pfizer (New York, NY)
- …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... the reporting of clinical trial results to regulatory authorities and the scientific community by contributing to the clinical study reports, clinical … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to ... communication skills. + Solid knowledge of statistical analysis methodologies, experimental and clinical trial design + Expertise in statistical software Does… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments + Assists with and may author/review ... process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including… more
- Hackensack Meridian Health (Hackensack, NJ)
- …change. The ** Clinical Research Nurse** is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in ... Preferred: + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology (QP) group. The AD will lead model-informed drug development ... combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.… more
- Hackensack Meridian Health (Hackensack, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education, Knowledge, Skills and ... : + SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …consequences of discovered disease gene variants + Understanding of drug development and clinical trial design and execution. Experience in the clinical ... You will collaborate with various RGC teams and with pre- clinical and clinical development teams at Regeneron to catalyze therapeutic development for… more
- TD Bank (New York, NY)
- …by covered companies, drug mechanisms and their associated safety/efficacy profiles, clinical trial design strategies, etc.) and non-scientific (analyzing ... TD Cowen, a division of TD Securities, is looking for an Equity Research Associate to join its Healthcare, Biotechnology team in New York. Equity Research Analysts… more
- Mount Sinai Health System (New York, NY)
- …leaders, hospital and system leaders, and with external parties. **Grant and Clinical Trial Management** + Responsible for research enterprise including grants ... of current and new faculty + With the Site Associate Chair of Administrative Affairs, oversee and administer faculty...research compliance, and oversight of core facilities + Oversee clinical research and clinical trial … more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …accepting this position, you will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness and whether your continued employment ... would advance the efficiency of the Federal service. Upon completion of your trial period, your employment will be terminated unless you receive certification, in… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …employment for accepting this position, you will be required to serve a 2-year trial period during which we will evaluate your fitness and whether your continued ... efficiency of the Federal service. Upon completion of your trial period, your employment will be terminated unless you...format of a health records. OR, (2) Education. An associate 's degree from an accredited college or university recognized… more
- Mount Sinai Health System (New York, NY)
- …color + Supportive and experienced clinical staff + State of the art clinical trial unit, clinical and translational research environment and affiliated ... and expertise in skin of color, as director and associate director of the skin of color center, respectively,...candidates, given that our department is a leader in clinical and translational research in skin of color to… more
