- 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
- Sumitomo Pharma (Trenton, NJ)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Parexel (Trenton, NJ)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- Taiho Oncology (Princeton, NJ)
- …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- Parexel (Trenton, NJ)
- …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- System One (Basking Ridge, NJ)
- …M-F Day Pay: $30-34/hour Responsibilities: + Monitor and assess temperature data for clinical trial shipments and on-site storage. + Collaborate with Quality to ... Title: Clinical Supplies Associate Location: Basking Ridge,...destruction, study close-out, and filing documents in the electronic Trial Master File (e-TMF). Requirements: + Background in pharmaceutical… more
- Bristol Myers Squibb (Princeton, NJ)
- …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial /biomarkers and asset development as well as ... late-stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written… more
- Sumitomo Pharma (Trenton, NJ)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … 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
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Description: Oncology Clinical Biomarker Lead ( Associate /Director), Translational Development** ... biology, mechanism of action, and predictive biomarkers in our late-stage clinical oncology portfolio. Ideal candidates will possess a strong scientific background,… 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
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …As core study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of... clinical , statistical, and regulatory literature for current clinical trial results, regulatory trends and new… more
- Parexel (Trenton, NJ)
- …in Lupus is preferred *Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
- Merck (Trenton, NJ)
- … Associate (CRAs), Clinical Research Managers (CRMs), in the Global Clinical Trial Operations (GCTO) Regions in alignment with strategic priorities for ... **Required Knowledge and skills:** + Strong knowledge of drug development and clinical trial processes, including relevant standards and documentation. +… more
- System One (Princeton, NJ)
- …RAVE). + Lead data reporting and BI efforts, including graphical dashboards to support clinical trial progress and operational KPIs + Ensure compliance with CFR ... Job Title: Associate Director of IT - Life Sciences/ Clinical...technical staff and non-technical business stakeholders + Familiar with clinical systems and trial platforms such as… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …team. In addition to regulated bioanalysis, innovative measurement projects that focus on clinical trial outcomes and process improvement are just a part of ... as biospecimen management. In addition, he/she will be responsible for surveying the clinical trial measurement landscape and make recommendations on process and… more
- Sumitomo Pharma (Trenton, NJ)
- …regulatory submissions and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to ... a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part… more
- ThermoFisher Scientific (Lawrenceville, NJ)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …+ Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial , and public domain information resources to identify ... The Associate Director of Regulatory Intelligence leads the collection...taxonomy terms relevant to Otsuka approved and investigational products, clinical , and business development programs. + Build professional network… 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