WalthamFull TimeHealthcare
Remotely
gcppharmacovigilanceclinical trialsclinical developmentregulatoryclinical study reports
Job Description
📋 Description
- Leads direction, planning, execution, and interpretation of clinical trials or research activities
- Participates in cross-functional teams to generate and disseminate high-quality clinical data
- Oversees study teams, ensures enrollment and timelines, and reviews safety/efficacy data.
- Leads design, analysis, and reporting of protocols, regulatory submissions, and program documents.
- May supervise Medical/Scientific Directors and Clinical Scientists.
- Joins Clinical Strategy Teams to develop rigorous Clinical Development Plans.
🎯 Requirements
- MD/DO or non-US equivalent; subspecialty fellowship desirable.
- 5-7 years clinical trial experience in pharma/academia; ability to run complex programs.
- Proven leadership and cross-functional collaboration skills.
- Strong knowledge of clinical trial methodology, regulatory/compliance requirements, and clinical
- Excellent oral and written English communication.
- Ability to address complex problems and provide solutions for multiple projects.
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