Hiring company: Gilead
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.
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.
Clinical Trials Manager, Clinical Operations – (CTM) - Oncology
Specific Responsibilities and Skills for Position:
- Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports
- Must be able to understand, interpret and explain protocol requirements to others
- Maintains study timelines
- Coordinates review of data listings and preparation of interim/final clinical study reports
- Assists in determining the activities to support a project’s priorities within functional area
- Contributes to development of RFPs and participates in selection of CROs/vendors
- May be asked to train CROs, vendors, investigators and study coordinators on study requirements
- Contributes to development of study budget
- May serve as a resource for others within the company for clinical trials management expertise
- Able to examine functional issues from an organizational perspective
- Participates in the recruiting and hiring process for CPA/CTMA/Sr. CTMA and support their professional development
- May contribute to development of abstracts, presentations and manuscripts
- Under supervision, may design scientific communications within the company
- Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision
- Must have a general, functional expertise to support SOP development and implementation
- Travel may be required
Knowledge:
- Excellent teamwork, communication, decision-making and organizational skills are required
- Thorough 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
Experience and Skills:
- At least 5+ years of experience and a RN (2 or 3 year certificate) or BS/BA in a relevant scientific discipline
- At least 3+ years of experience and a Masters' degree or higher; scientific discipline preferred
- Prior oncology clinical trials experience is preferred