Title: Clinical Project Manager
Location: Santa Clara, California
Duration: 12+ Months
Job Description:
Working with diverse groups such as Regulatory Affairs, Program Management, Research & Development, Quality Assurance and external clinical contractors the primary role of this position is the facilitation and management of APOC’s Clinical Study program.
Responsibilities:
- Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations.
- Oversees development of clinical documents, including clinical plans, protocols, forms, and reports.
- Manages team to prepare for clinical study initiation, execution and close out activities.
- Monitors and reports progress of clinical studies and follows up with team members and line managers when issues develop.
- Communicates and works with cross-functional teams to resolve issues that arise during clinical studies.
- Ensures consistency of clinical study and processes across clinical trials.
- Travels as necessary to aid in program facilitation.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.