- Lilly (Indianapolis, IN)
- …to Lilly's drug development needs! In partnership with the Asset team, the ** Senior Director, Clinical Design Program Lead** will lead a cross-functional group in ... cost, and time). + Represent program and trial design optionality to asset teams and Sr . Leaders to inform prioritization of an option that will be translated into a… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …Director, you will provide clinical oversight to multiple clinical trials. Additionally, the Senior Director guides the project teams to design and implement ... of study conduct and industry standards of Good Clinical Practice. + Lead project teams to design and implement clinical studies. + Write protocols, investigator… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** As Sr . Director of Clinical development in the Inflammation/Fibrosis therapeutic area, you ... including but not limited to assessment of eligibility criteria, addressing investigator questions, safety monitoring, and ensuring high data quality through data… more
- Taiho Oncology (Princeton, NJ)
- …area issues and questions + Set up and lead advisory boards + Review investigator -sponsored study (IIST) proposals and other research grants + Provide medical ... Sr . Medical Director, Medical Affairs Princeton, NJ, USA...matter expert + Collaborate with key cross-functional partners on project teams to ensure the development of scientifically accurate… more
- Medexus Pharma (Remote, OR)
- …centers of excellence engagement plans. + Facilitate the submission of investigator -initiated trials and collaborative research inquiries, including the ... Medical Science Liaison/ Sr . MSL/ Principal MSL remote Remote, Great Lakes/...thought leaders, and key stakeholders to exchange clinical and research insights on Medexus products. This role builds and… more
- AbbVie (Nashville, TN)
- …Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Medical Science Liaison (MSL/ Sr MSL), is a field based scientific expert that strategically ... executes and maintains high impact territory plans, including HCP and Investigator engagement plans in alignment with therapeutic area medical and scientific… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …writing activities as needed. + Represent the medical writing function on product or project teams with oversight from senior staff. + Participate in submission ... _This role is located in Santa Monica CA._ As Sr Medical Writing Associate you will be responsible for...1 and Phase 2 Clinical Study Reports (CSRs) and Investigator 's Brochures (IBs) in compliance with regulatory requirements and… more
- System One (Park Ridge, NJ)
- Title: Sr Regulatory Writer - R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing ... device, cosmetic, disinfectant (EPA, DIN) and general household products areas. The Senior Writer will lead and drive the technical (CMC) writing to accelerate… more
- Geisinger (Danville, PA)
- …candidate will enjoy 80% protected research time along with dedicated research support staff including project management and biostatistical support. The ... of CKD, cardiovascular-kidney-metabolic syndrome, and patient-centered care. Resources include research data analyst support, project manager, project… more
- Chiesi (Cary, NC)
- …identify new collaborative KOL relationships for advisory boards, company-sponsored, investigator -initiated research , and speaker development + Provide beliefs, ... scientific meetings + Provide field-based medical affairs assistance for clinical research initiatives supported by Company, related to Investigator Initiated… more