- Bayer (Whippany, NJ)
- …the creation of clinical documents or components of key documents (eg, Clinical Study Protocol, Investigator Brochure, Clinical Study Report, regulatory ... across the organization and externally with service providers and investigator sites; + Review clinical trial data...service providers and investigator sites; + Review clinical trial data both internally and from external vendors/partners,… more
- Arvinas (New Haven, CT)
- …and external) on study design elements and endpoints + Contribute to the clinical portion of investigator brochures review for consistency and applicability + ... and medical literature to support document development, such as the investigator brochure, protocol design, clinical study report, competitive assessments,… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …(IP) review and accountability on site. * Serves as point of escalation for clinical site management and investigator sites. Liaises with the in-house CRA ... knowledge of trial oversight activities, GCP/ICH and federal regulations, IRB/EC and Investigator responsibilities. * Familiarity with clinical trial systems (ie… more
- Actalent (Neenah, WI)
- … clinical research protocols under the general supervision of the Principal Investigator or Clinical Research Manager responsible for the clinical ... Healthcare Clinical Study Specialist Job Description A Clinical Study Specialist is a professional who will coordinate and oversee clinical operations of… more
- Amgen (Thousand Oaks, CA)
- …input/review study start up documentation, eg, CRF design + Attend and provide clinical support for investigator and steering committee meetings + Participate in ... transform the lives of patients while transforming your career. **Executive Director, Clinical Development, Rare Disease** **Live** **What you will do** Let's do… more
- Taiho Oncology (Pleasanton, CA)
- …the reports or the appropriate sections of the following documents: + + Clinical Study Reports. + Investigator Brochures. + Population PK and/or ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Carle Health (Urbana, IL)
- …dollar investment in its research infrastructure, including CCIRP, CIAIC, clinical trials management, investigator -initiated support services, and other ... Overview The Stephens Family Clinical Research Institute of the Carle Foundation Hospital...Foundation Hospital in Urbana, IL is building the Carle Clinical Imaging Research Program (CCIRP) with a position to… more
- Teva Pharmaceuticals (Parsippany, NJ)
- … documents including but not limited to clinical study protocols, clinical study reports, investigator 's brochures, and summary modules for regulatory ... Medical Writing Clinical Publisher Date: Nov 7, 2025 Location: Parsippany,...difference with. **The opportunity** The primary responsibilities of the Clinical Publisher ( Clinical Publisher) are to ensure… more
- Ascendis Pharma (Palo Alto, CA)
- …study teams + Ensure successful completion of trial-related documents (including clinical trial protocols, investigator brochures, medical monitoring plans, site ... the design, monitoring, data analysis, and interpretation of the Company's late-phase clinical trials in endocrinology. As such, the Medical Director is an important… more
- Ascendis Pharma (Palo Alto, CA)
- …and subject retention + Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training ... a dynamic workplace for employees to grow and develop their skills. The Senior Clinical Scientist is involved in the design, monitoring, and data analysis of the… more