South San FranciscoFull TimeHealthcare
Remotely
gcppharmacovigilanceclinical developmentregulatory submissionsclinical study reports
Job Description
📋 Description
- Oversees direction, planning, execution, and interpretation of clinical trials for development
- Leads design/implementation of programs aligned with Product Development Plan.
- Ensure study integrity; interpret safety/efficacy data for molecule.
- Manage study enrollment timelines and key deliverables; report SAEs per policy.
- Provide in-house clinical expertise; coordinate translational strategies as needed.
- Stay updated on regulatory requirements and GCP standards.
🎯 Requirements
- MD/DO or non-US equivalent; residency preferred; subspecialty fellowship desirable.
- At least 2 years of clinical trial experience in pharma/academic.
- Ability to run a cross-functional global clinical research program.
- Ability to interact to support global scientific/business strategy.
- Knowledge of trial methodology and regulatory/compliance requirements.
- Excellent oral and written English communication skills.
🎁 Benefits
- Comprehensive benefits: PTO, medical/dental/vision insurance, 401(k).
- Eligible for long-term incentive programs.
- AbbVie is an equal opportunity employer.