- Bristol Myers Squibb (San Diego, CA)
- …personal lives. Read more: careers.bms.com/working-with-us . RayzeBio, a Bristol Myers Squibb company , is a dynamic biotechnology company headquartered in San ... of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial… more
- Bristol Myers Squibb (San Diego, CA)
- …. **Clinical Development Lead Prostate (ACP3)** RayzeBio, a Bristol Myers Squibb company , is a dynamic biotechnology company headquartered in San Diego, ... to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …US Medical Senior Director, MA Evidence Generation at Kite Pharma, a Gilead Company , will provide scientific and strategic leadership for the design, execution, and ... with Medical and Clinical development teams. + Oversee the US Investigator -Sponsored Research (ISR) and Collaborative Research (CR) program within the evidence… more
- Kelly Services (Irvine, CA)
- …Research Leader within the Clinical R&D Department to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, ... the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures; + May serve as the primary contact for… more
- Arvinas (New Haven, CT)
- Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the ... PROTAC protein degraders against validated and "undruggable" targets, the company has three investigational clinical-stage programs currently enrolling: ARV-102 for… more
- Teva Pharmaceuticals (West Chester, PA)
- …(REMOTE) Date: Nov 22, 2025 Location: West Chester, United States, Pennsylvania, 00000 Company : Teva Pharmaceuticals Job Id: 64152 **Who we are** Together, we're on ... edits clinical regulatory documents (eg, study reports, protocols, briefing books, investigator 's brochures, health authority responses, Module 2.5 and 2.7.x). +… more
- United Therapeutics (Research Triangle Park, NC)
- …as follows:** **Who We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... complex aspects of protocol design and/or study data at investigator and internal meetings + Prepare and review draft...literature + Collaborate with Medical Science Liaisons and other company staff in identifying key partners for future research… more
- Bristol Myers Squibb (Princeton, NJ)
- …prepares study protocols, amendments, specific sections of study manuals and Investigator meeting materials, and other documents as needed with appropriate guidance ... the preparation/review of INDs, regulatory documents, IND annual report/DSURs, Investigator Brochures, and NDAs/MAAs. + Supports priorities within functional area.… more
- Astellas Pharma (Northbrook, IL)
- …this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are ... closely with safety officer in writing and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events. +… more
- Lilly (Boston, MA)
- …design and development of key clinical documents, including study protocols, investigator 's brochures, informed consent documents, and other essential materials. + ... a key medical expert in cross-functional discussions, including regulatory submissions, investigator meetings, and advisory boards. + Work with the Clinical… more