3410 Clinical Trial Manager Clinical Operations

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 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.

Education:
Minimum BA/BS.
7 years of 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.).

PLEASE NOTE: Our client has mandated COVID-19 vaccination for their workforce, all external personnel providing services to our client are required to comply with this requirement.