WalthamFull TimeHealthcare
Remotely
gcponcologyclinical trialsregulatoryclinical study reportspkpd
Job Description
📋 Description
- Manages the design and implementation of one or more clinical development programs in support of an
- Has overall responsibility for oversight of clinical studies, monitoring overall study integrity
- Responsible for design, analysis, interpretation, and reporting of scientific content of protocols
- May oversee the work of Associate Medical, Medical and/or Scientific Directors working on the same
- Provides in-house clinical expertise for the molecule and disease, coordinating appropriate
- May serve on or chair a Clinical Strategy Team (CST), with responsibility for development of a
🎯 Requirements
- Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with
- At least 3 years of clinical trial experience in the pharmaceutical industry, academia, or
- Ability to run clinical research program(s) of moderate complexity with minimal supervision.
- Ability to interact externally and internally to support a global scientific and business strategy.
- Experience in drug development in thoracic malignancies and/or T-cell engagers strongly preferred.
- Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical
🎁 Benefits
- AbbVie is an equal opportunity employer and is committed to operating with integrity, driving
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick)
- This job is eligible to participate in our long-term incentive programs.
- US & Puerto Rico only - to learn more, visit the provided resources on equal employment
- Compensation and benefits are described in the posting and may be modified at the Company’s