Remotely
gcpregulatory complianceclinical trial designclinical study reportsgood clinical practices
Job Description
📋 Description
- Oversee direction, planning, and interpretation of clinical trials in a development program.
- Participate in cross-functional teams to deliver high-quality clinical data.
- Design study protocols aligned with regulatory and scientific needs.
- Monitor study integrity, safety, and efficacy data with oversight from Clinical Operations.
- Contribute to interpretation and reporting for regulatory submissions.
- Engage in cross-functional Clinical Strategy and leader interactions as needed.
🎯 Requirements
- Medical Doctor (MD) or DO or non-US equivalent with relevant specialty.
- Experience running clinical research with supervision.
- Strong collaboration and cross-functional teamwork.
- Clinical trial experience in pharma, academia, or equivalent preferred.
- Knowledge of trial design, regulatory/compliance, and GCP.
- Excellent English communication skills.
🎁 Benefits
- AbbVie offers comprehensive benefits package.
- Eligible for long-term incentive programs.
- Competitive pay aligned with location and grade.
- Equal opportunity employer and inclusive culture.