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About the Role
This position serves as the affiliate’s medical and scientific expert for assigned products and therapeutic areas, with a primary focus on real-world evidence generation. The role partners with internal and external stakeholders to develop evidence concepts and protocols, support study execution, and strengthen the scientific foundation of therapeutic areas. It also supports the identification, review, and management of Investigator-Initiated Studies (IIS), while engaging with external stakeholders to exchange scientific insights and advance evidence generation strategies.
Responsibilities
- Contribute to and support the medical strategy for the assigned therapeutic area, with emphasis on real-world evidence generation.
- Collaborate with the TA/MSL medical team, Evidence Solutions Group, and other relevant internal and external stakeholders to develop evidence concepts, study proposals, protocols, and IIS-related activities.
- Support the planning, review, and management of real-world evidence generation activities and IIS in alignment with internal standards and applicable procedures.
- Establish and maintain professional relationships with external stakeholders, including academic experts and other relevant partners, to support evidence generation and scientific exchange.
- Review and synthesize relevant scientific literature, congress data, and external insights to identify evidence gaps, scientific trends, and opportunities relevant to the therapeutic area.
- Serve as a scientific resource for the assigned therapeutic areas, including responding to medical and scientific information requests and contributing to core medical materials and dossiers.
- Ensure all activities are conducted in compliance with applicable laws, regulations, industry codes, and AbbVie standards and policies.
Requirements
- Knowledge of medical science and regulations
- Excellent oral and written English communication skill
- Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols
- Experience in a pharmaceutical company over 3 years
Skills
- Medical science
- Regulations
- Oral communication
- Written English communication
- Clinical trial methodology
- Regulatory requirements governing clinical trials
- Development strategy
- Protocol design
- Real-world evidence generation
- Scientific exchange
- Scientific literature review
- Data synthesis
- Medical information requests
Experience Level
- Workday Global Grade: 16
Education Level
- Ph.D. – Desirable
- Bachelor or Master of Science – Required
About the Company
- AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.
- We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
- For more information about AbbVie, please visit us at www.abbvie.com.
- Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Equal Opportunity
- AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
- Equal Opportunity Employer/Veterans/Disabled.
- US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
- US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html