Remotely
oncologypharmacovigilanceregulatory complianceclinical trialsresearch & developmentcell therapymedical monitoringdata review
Job Description
📋 Description
- Manages the design and implementation of one or more clinical development programs in support of an
- Oversees project-related education of investigators, study site personnel and AbbVie study staff
- Has overall responsibility for oversight of 1-2 clinical studies, monitoring overall study
- Along with Clinical Operations, is responsible for oversight of study enrollment and overall
- Responsible for design, analysis, interpretation, and reporting of scientific content of protocols
- May oversee the work of Associate Scientific Directors and/or of Clinical Scientists working on the
🎯 Requirements
- Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, PharmD) preferred
- Ability to provide input and direction to clinical research with appropriate supervision
- At least 5+ years of clinical trial experience in the pharmaceutical industry, academia, or
- Ability to oversee a clinical research program of moderate complexity with minimal supervision
- Ability to perform and bring out the best in others on a cross-functional global team
- Ability to interact externally and internally to support a global scientific and business strategy
🎁 Benefits
- 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
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