Immediate Need for Senior Clinical Project Manager with a biotech company in Boston, MA. This is a full time permanent position. Remote 3 days, office based 2 days a week.
Must have small biotech experience, Phase I-III management experience, CRO oversight and international experience.
Rare disease is preferred but not required.
Sr. Clinical Project Manager (CPM) provides operational leadership of one or more clinical trials from protocol development through clinical study report, and ensure activities are executed in accordance with the protocol, ICH/GCP guidelines, applicable regulations, and company's policies and procedures and corporate goals. Responsibilities may include leading cross-functional study team(s) and/or the oversight of Contract Research Organizations (CRO) and vendors. The CPM will have a command of assigned studies, the ability to flex and adapt to dynamic situations, and will utilize critical thinking skills to facilitate risk mitigation analyses and problem solving.
Reporting Relationship
The Clinical Project Manager or Sr. Clinical Project Manager will report to the Vice President of Clinical Operations or designee
Duties and Responsibilities
Educational Qualifications
A Bachelor's degree or higher degree (scientific discipline preferred)
Additional Qualifications
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