Principal Scientist overseeing clinical program execution at a bio-pharmaceutical company. Leading cross-functional teams in clinical development activities from strategic planning to post-marketing approval.
Responsibilities
Provide oversight and leadership of clinical program execution.
Lead and direct global, cross-functional teams in end-to-end clinical development activities (strategic planning through post-marketing approval).
Responsible and accountable for the operational execution of a suite of clinical trials encompassing a clinical program.
Lead and direct teams to support key program planning and execution elements.
Serve as the operational representative on the Product Development’s Clinical Subteam.
Collaborate and facilitate interactions with key internal and external stakeholders (e.g., KOLs, supplies) in support of clinical program objectives.
Requirements
Bachelor's Degree +12 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR master's degree +9 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
Degree in life sciences, preferred.
Highly Preferred: experience in leading clinical programs for Gastroenterology, Dermatology, Pulmonary or Rheumatology, especially autoimmune or immune-mediated disorders.
Experience in leading global clinical programs, including trial initiation through database lock.
Experience in developing protocols and study related documents for Immunology related clinical trials.
Benefits
medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days
Job title
Principal Scientist, Clinical Operations, Immunology
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