- Actalent (Lexington, MA)
- Job Title: Clinical Trial Associate As a Clinical Trial Associate , you will support clinical operations and contribute to groundbreaking ... + Support clinical research operations and ensure compliance with clinical trial protocols. + Maintain and organize clinical documentation. + Collaborate… more
- Sumitomo Pharma (Concord, NH)
- …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 (Concord, NH)
- …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
- Parexel (Concord, NH)
- …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
- Sumitomo Pharma (Concord, NH)
- …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
- Otsuka America Pharmaceutical Inc. (Concord, NH)
- …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 (Concord, NH)
- …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
- Sumitomo Pharma (Concord, NH)
- …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
- Otsuka America Pharmaceutical Inc. (Concord, NH)
- …+ 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
- Veterans Affairs, Veterans Health Administration (Bedford, MA)
- …per week. Responsibilities The duties and responsibilities are carried out in all clinical and other patient care areas involved with the Audiology service.. The ... health technician supports the function of the clinical programs in Audiology. The incumbent is a staff...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- Otsuka America Pharmaceutical Inc. (Concord, NH)
- …adheres to the approved core scientific narrative and lexicon, accurately reflects clinical trial data, and maintains consistency across global materials + ... on the execution and production of scientific assets, ensuring they accurately reflect clinical data, adhere to the core scientific narrative, and are compliant with… more