Senior Clinical Trials Manager, Clinical Operations - Oncology

CLINICAL OPERATIONS: Clinical Operations is responsible for the execution of all Phase 1-4 clinical trials, across all therapeutic areas, around the world. In partnership with Clinical Research, Medical Affairs and Development Operations functions, ensures that all clinical trial activities are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of Gilead’s products.

Senior Clinical Trials Manager, Clinical Operations- Oncology (Sr. CTM)

We are seeking a talented, experienced, and highly motivated candidate to join the Oncology Clinical Operations team. The candidate must have the ability to work independently, be an effective leader, and an engaged team member in a dynamic, fast-paced environment.

**This position can be located in Foster City, CA, Morris Plains, NJ, Seattle, WA or remotely in the US.
Specific Responsibilities and Skills for Position:

• Ability to write study protocols, study reports, sections for investigator brochures and regulatory documents (e.g. IND, NDA, etc.) with little supervision
• In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines
• Communicates with functional peers regarding project status and issues and ensure project team goals are met
• Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction
• Provide guidance and training to CROs, vendors, investigators and study coordinators on study requirements
• Anticipates obstacles and client difficulties and implements solutions to achieve project goals
• Experience in developing RFPs and selection and management of CROs/vendors
• May contribute to development of abstracts, presentations and manuscripts
• Functional expertise to initiate, author or contribute to SOP development, implementation and training
• Participates in the recruiting and hiring process for CPA/CTMAs and supports their professional development
• May manage CPA/CTMA/Sr. CTMA
• Coaches members of a work team and ensures adherence to established guidelines
• Ability to examine functional issues from a broader organizational perspective
• Excellent interpersonal skills and demonstrated ability to lead is required
• Independently manages less complex studies
• Travel may be required

Knowledge:

• Knowledge of FDA and/or EMA Regulations (or relevant local regulations), ICH Guidelines, and GCP governing the conduct of clinical studies
• Working knowledge and experience with Word, PowerPoint and Excel
• Excellent interpersonal skills and demonstrated ability to lead is required
• Excellent verbal, written, interpersonal and presentation skills are required
• Strong communication and influence skills and ability to create a clear sense of direction is necessary

Experience and Skills:

• At least 6+ years of experience and a RN (2 or 3 year certificate) or BS/BA in a relevant scientific discipline
• At least 4+ years of experience and a Masters' degree or higher; scientific discipline preferred

For Colorado Job Applicants: The salary range for this position is:

Gilead considers a range of factors, including background and experience, when determining base compensation. These considerations means actual compensation will vary. 
Position is also eligible for bonus and benefits. For more information, visit https://www.gilead.com/careers/compensation-benefits-and-wellbeing