Remotely
regulatory complianceclinical developmentgood clinical practiceclinical study reports
Job Description
📋 Description
- Oversees direction, planning, execution, and interpretation of clinical trials or research
- Participates in cross-functional teams to generate high-quality clinical data supporting product
- Designs and implements clinical development programs aligned with regulatory requirements and
- Oversees study enrollment, timelines, and data safety/efficacy assessments in collaboration with
- Provides clinical expertise for molecule/disease, coordinating with internal stakeholders and
🎯 Requirements
- Medical Doctor (M.D.), D.O., or non-US MD-equivalent with relevant specialty. Residency and
- At least 2 years of clinical trial experience in pharma, academia, or equivalent.
- Ability to lead a cross-functional global clinical research program with minimal supervision.
- Strong collaboration, communication, and regulatory knowledge for global development.
- Excellent English oral and written communication skills.
🎁 Benefits
- AbbVie comprehensive benefits package and competitive compensation.
- Eligibility for long-term incentive programs.
- Equal opportunity employer; commitment to integrity and inclusion.