ChicagoFull TimeHealthcare
Remotely
gcppharmacovigilanceclinical trialsregulatorycsrssaeclinical study reportsstudy protocols
Job Description
📋 Description
- Oversee direction, planning, execution and interpretation of clinical trials or research activities
- Manage design/implementation of study protocols within the Product Development Plan; supervise
- Oversee study enrollment, timelines, data safety and efficacy assessments; monitor SAEs per
- Contribute to design, analysis and reporting of protocols, CSRs, regulatory submissions and
- May serve on Clinical Strategy Team; help develop a rigorous Clinical Development Plan.
- Engage in opinion leader interactions and stay current on scientific/clinical developments.
Qualifications
- Medical Doctor (M.D.) or D.O. or non-US equivalent with relevant specialty; residency strongly
- Clinical trial experience in industry/academia; ability to run studies under supervision.
- Strong cross-functional collaboration skills and English communication proficiency.
- Bachelors (and advanced degree preferred for Scientific Director)
- Experience with regulatory requirements, trial design, and cross-functional strategy is desirable.
🎁 Benefits
- AbbVie comprehensive benefits package including PTO, medical/dental/vision, 401(k).
- Eligibility for long-term incentive programs.
- Equal opportunity employer; supports diversity and inclusion.