WalthamFull TimeHealthcare
Remotely
gcppharmacovigilanceclinical trialsregulatoryclinical study reportsstudy protocols
Job Description
📋 Description
- Oversee design, execution and interpretation of clinical trials.
- Participate in cross-functional teams to deliver high-quality data.
- Ensure GCP/regulatory compliance in trials.
- Manage study protocols and timelines.
- Contribute to the Clinical Development Plan.
- Engage with thought leaders and Medical Affairs as required.
🎯 Requirements
- Medical Doctor (M.D.), Doctor of Osteopathy (D.O.), or non-US equivalent; residency strongly
- Ability to run a clinical research study with supervision.
- Strong desire to collaborate in a cross-functional setting.
- Clinical trial experience in pharma/academic environment preferred.
- Knowledge of clinical trial methodology and regulatory/compliance; experience in protocol design.
- Excellent oral and written English communication skills.
🎁 Benefits
- Competitive compensation package.
- Comprehensive benefits including PTO and medical/dental/vision insurance; 401(k).
- Eligibility for long-term incentive programs.
- AbbVie is an Equal Opportunity Employer.