We have a current opportunity for a Clinical Trial Manager, Clinical Operations on a 12- month contract basis. The position will be based in San Rafael, CA. For further information about this position please apply.
Duties: For the assigned study(ies), the Study Manager is accountable for day-to-day Clinical Operations study execution and related deliverables and is the primary point of contact within Clinical Operations for a study. Key responsibilities include managing risks, issues, and opportunities that impact timeline, quality, and budget, overseeing the Clinical Operations study team, vendors, and CRO, and collaborating with cross-functional representatives to execute on study deliverables.
Skills: The candidate is expected to show and have proficiency and experience in the following competencies:
Decision Making, Strategic Thinking, and Problem Solving Influence and Organizational Awareness Agility and Proactivity Communication and Collaboration With advanced technical competencies in many of the following areas:
Study Management and Execution
Compliance and Quality Data Analysis and Interpretation Drug Development and Study Design
Product and Therapeutic Area Knowledge
7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO Experience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.)