Clinical Scientist
Medasource
- New York, New York, United States
- New York, New York, United States
Über
Clinical Scientist Remote 6 month contract with extensions The Clinical Scientist, Rheumatology will be responsible for assisting in the development and execution of Medical Affairs sponsored and supported clinical programs for company products in the Rheumatology therapeutic area. The Clinical Scientist will partner with other Rheumatology team members, as well as real-world evidence, health economic and outcomes research, biostatistics, and commercial marketing personnel to formulate and execute scientific strategy on marketed products as well as address other medical questions and issues that arise from the field. Responsibilities: Responsible for the development and execution of Medical Affairs sponsored and supported clinical programs for company products in the Rheumatology therapeutic area. Lead the day-to-day conduct of clinical studies of all types, including Phase IIIb/IV trials, registries, real-world evidence, collaborations, and investigator-initiated studies. Actively partner with individuals in the Dermatology therapeutic area and other groups inside and outside Medical Affairs to support analysis plans, safety data review for database locks, and ensure compliance with study monitoring and other SOP/GCP requirements. Contribute as a subject matter expert on previous and new data on approved immunology products, providing advice and input to the Integrated Evidence Teams, Commercial, and Medical Information Teams. Contribute to or lead the development of study reports, abstracts, and manuscripts, with a focus on safety analyses and experience. Build and manage effective relationships with KOLs and investigators related to Medical Affairs studies and strategic initiatives. Qualifications: MA/MS/PharmD/PhD preferred, ideally with a focus on basic or medical science, public health, and/or epidemiology. This position requires a minimum of 3 years of pharmaceutical industry experience with at least 2 years of clinical study, registry, or real-world evidence study experience strongly preferred. Overall, the position requires 8-10 years of work experience in total. Experience with clinical studies end-to-end conduct (e.g., protocol development, study planning/start-up/execution/close-out) and study medical monitoring/safety reporting is required. Experience with data analysis, review, and results interpretation is preferred. Strong organizational skills, written and verbal communication skills are required. Excellent time management skills with the proven ability to plan and track deliverables and timelines are required. Ability to work in a matrix environment with cross-functional teams is mandatory. Energy and enthusiasm, strong leadership skills, and the ability and desire to embrace building subject matter expertise are essential. Seniority level
Associate Employment type
Full-time Job function
Science, Research, and Strategy/Planning Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Sprachkenntnisse
- English
Hinweis für Nutzer
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