WalthamFull TimeHealthcare
Remotely
gcppharmacovigilanceregulatory complianceclinical trialsprotocol designmddoclinical study reports
Job Description
📋 Description
- Oversee direction, planning, execution and interpretation of clinical trials in a development
- Participate in cross-functional teams to generate and interpret high-quality clinical data for
- Design and implement study protocols; supervise investigators and site personnel.
- Monitor study integrity and review data for safety and efficacy; manage enrollment and timelines.
- Contribute to protocol design, Investigator Brochures, Clinical Study Reports and regulatory
🎯 Requirements
- MD/DO or non-US equivalent with relevant specialty; residency preferred; subspecialty fellowship
- Experience in running clinical research studies and collaboration in cross-functional teams.
- Clinical trial experience in pharma, academia or equivalent; knowledge of trial methodology and
- Ability to interact to support global scientific and business strategy; strong English
- Ability to design study protocols and support regulatory discussions.
🎁 Benefits
- Competitive compensation package with comprehensive benefits including PTO, medical/dental/vision
- Eligibility to participate in long-term incentive programs.
- AbbVie is an Equal Opportunity Employer; see company information for details.