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
Senior CRA overseeing clinical trial activities to ensure compliance with protocols in China. Collaborating with teams and site personnel to enhance trial execution and data integrity.
Clinical Operations Study Country Lead overseeing US clinical trials at Sanofi. Leading strategic planning, execution, and ensuring compliance with regulations and digital transformation initiatives.
Manager, Clinical Operations at Nuvalent overseeing clinical trial planning, execution, and data collection according to regulatory guidelines. Responsible for various aspects of clinical study conduct and ensuring high - quality results.
CRA Manager responsible for oversight, coaching, and performance management of CRA teams to meet clinical trial KPIs. Focused on delivery, quality, and compliance for clinical research in China.
Vice President driving operational excellence and strategy for Sitero’s clinical services. Leading teams and ensuring compliance across global clinical operations.
Vice President of Clinical Operations at knownwell leading national clinical teams in obesity medicine. Responsible for building team culture, achieving best - in - class clinical outcomes, and driving performance in healthcare settings.
Head of Clinical Operations overseeing clinical governance and operations at CARED, a health - tech revolutionising allied health. Opportunity to shape the future of care in Australia and beyond.
Clinical Operations Coordinator ensuring quality patient care and compliance in home health agency. Collaborating with interdisciplinary teams while supporting field staff in multiple locations.
Clinical Operations Asset Lead overseeing operational strategy and execution within clinical research at GSK. Driving informed decision - making and ensuring high‑quality, on‑time delivery throughout the asset lifecycle.