Role Summary
Regional Medical Science Director (MSL) is a field-based scientific expert who supports scientific and business objectives for cancer therapeutics across the product life cycle. They are the primary communicators of Summit Therapeutics science within a defined geography to healthcare professionals and researchers, with a focus on Immuno-Oncology and treatment options. They collaborate with cross-functional teams to support clinical development and pipeline activities as needed. Must be located in the Mid-Atlantic states: New Jersey, Pennsylvania, Delaware, Maryland, Virginia, West Virginia, North Carolina, and South Carolina.
Responsibilities
- Develop, execute and maintain high impact territory plans, including HCP and Investigator engagement plans in alignment with therapeutic area medical and scientific objectives with a focus on quality
- Support clinical development and research initiatives across development at the request of R&D to include, but not limited to, site evaluation and identification, recruitment, investigator meetings, external expert identification, and involving experts to generate scientific data including investigator-sponsored trials
- Identify, gain access to, and develop professional customer centric based relationships with external experts in Immuno-Oncology within assigned geography
- Provide education relative to disease state, therapeutic landscape and Summit Therapeutics products across the product lifecycle to healthcare providers and researchers
- Participate, monitor, and provide insights to Summit from relevant scientific meetings in relevant geography
- Continuously maintain self-education on market issues/trends, product knowledge, and new therapeutic areas of interest as it pertains to specific business responsibilities, including creating awareness and relationships for Summit Therapeutics in the Medical community
- Actively participate in relevant team meetings, organizational activities, and Country-driven medical affairs activities (e.g. advisory boards, masterclasses, roundtables)
- Create, maintain, and collaborate in relationships with Cross-Functional partnerships, as appropriate, to develop and execute Account plans designed to support and meet shared scientific or business objectives
- All other duties as assigned
Qualifications
- A minimum of 5+ years of solid tumor cancer experience
- A minimum of 5+ years of clinical, scientific/research, or industry related experience or equivalent
- A minimum of 2+ yearsβ experience in Medical Science Liaison role
- Previous pharmaceutical industry experience within relevant scientific discipline is strongly preferred
- The MSL must possess and be able to demonstrate past achievements in:
- Understanding, analyzing and communicating complicated scientific concepts and data
- Building credible relationships with prominent HCPs
- Ability to independently identify and translate corporate needs into an action plan that will achieve objectives
- Self-motivation to achieve and exceed goals
- Problem solving and analytic skills
- Critical thinking
- Ability to work independently
- An essential requirement of the position is to meet health care industry representative (HCIR) credentialing requirements to gain entry into facilities and organizations that in your assigned territory. These HCIR credentialing requirements may include, but are not limited to, background checks, drug screens, and proof of immunization/vaccination for various diseases.
Skills
- Proficient user of standard MS Office suite (e.g., Word, Excel)
- Experience using electronic document management systems, and document review tools desirable
- Strong computer and database skills
- Attention to detail, accuracy and confidentiality
- Clear and concise oral and written communication skills
- Excellent organizational skills
- Must be able to effectively multi-task and manage time-sensitive and highly confidential documents
- Prioritize conflicting demands
- Work in a fast-paced, demanding and collaborative environment
Education
- Doctoral degree in the health sciences from an accredited university required (MD, PhD, PharmD, or equivalent). Significant clinical and/or industry experience in oncology and cancer therapeutic area may be accepted in lieu of education requirements.
Additional Requirements
- Must be willing to travel up to 75% of the time