Pipeline Medical Science Liaison, Hematology & Oncology

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Therapeutic area: Hematology, Oncology.

We are open to candidates residing in any location. 

This position covers operations across the entire country.

The Pipeline Medical Science Liaison (pMSL) is a field-based scientific expert dedicated to facilitating scientific dialogue and supporting the scientific, clinical and business objectives of a designated therapeutic area, with a strong focus on clinical research and enterprise critical studies globally. The pMSL role embodies our unified R&D approach by fostering seamless collaboration with in-house Clinical Site Monitoring (CSM) teams, especially Clinical Research Associates (CRAs). This integrated approach ensures the alignment of scientific vision and operational execution, enhancing the efficiency and effectiveness of pipeline development and acceleration.

The role emphasizes strong engagement with investigators, healthcare professionals, and key scientific institutions to elevate AbbVie's scientific credibility and support clinical research and development of investigational products and compounds. The pMSL serves as a conduit of information to a cross functional External Experts (EEs) regarding AbbVie’s investigational products, and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, code of conduct, AbbVie’s policies and procedures and accepted standards of best practice.

Key Responsibilities:

• Establish and maintain a strong scientific presence at investigational sites and key scientific centers.
• Act as an expert in the designated therapeutic area and deliver credible scientific presentations related to AbbVie pipeline products, including but not limited to study initiation trainings and scientific information support.
• Collaborate with Clinical Site Monitoring teams, especially Clinical Research Associates (CRAs) and Clinical Development, Oncology Early Development departments, and other relevant functions to support AbbVie-led clinical trials.
• Participate in country and site feasibility and selection process to help identify qualified external experts (EEs) for AbbVie clinical programs.
• Collaborate with Medical Affairs activities such as advisory boards, steering committees, congresses, and symposia.
• Offer scientific and business leadership to establish and maintain professional, credible relationships with investigators and thought leaders to facilitate potential research collaborations and educational efforts.
• Act as the primary contact for investigator-initiated study ideas and support interactions with both local and global medical teams.
• Maintain a high level of interaction with internal and external stakeholders to support scientific dialogue.
• Ensure all activities are conducted in compliance with relevant laws, guidelines, and AbbVie’s policies.

• Advanced degree in health sciences or clinical discipline required (e.g. PharmD., MD, PhD or MSc). Candidates with an undergraduate degree and significant relevant experience may be considered.
• Greater than or equal to 2 years of clinical, scientific/research, or industry related experience or equivalent strongly preferred.
• Experience in Hematology & Oncology and in an MSL or CRA (or similar) role with proven success may be considered as an additional asset.
• Ability to quickly learn about new subject areas and environments.
• Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general.
• Demonstrated expertise in the aligned therapeutic area, scientific methods, clinical research & development and current regulatory requirements.
• Excellent communication and presentation skills, with proficiency in scientific storytelling.
• Demonstrated ability to develop and maintain strong collaborative relationships.
• Demonstrated ability to work independently and as part of a cross functional team and in matrix environment.
• Fluent in Polish and English.
• Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.

Willingness to travel up to 50-75% of the time for field-based activities.
 

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