Job Description
Scientific Exchange:
- Develops professional relationships and engages with national and/or regional SLs to ensure access to medical and scientific information on areas of therapeutic interest and Company products.
- Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the Company.
- Addresses scientific questions and directs SL inquiries on issues outside of MSL scope (e.g., grants) to appropriate Company resources consistent with applicable policies.
- Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI).
- Upon request from Global Clinical Trial Operations (GCTO),
- Identifies barriers to patient enrollment and retention efforts to achieve study milestones, recommends study sites, and identifies potential investigators to participate in phase II-IV clinical development programs.
- Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies.
- Upon request from Scientific Affairs,
- Enhances the comprehension of the scientific foundations and goals of investigator-sponsored research.
- Identifies barriers to patient enrollment and retention efforts to achieve study milestones.
- Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
Scientific Congress Support:
- Engages in scientific and medical meetings through pre-congress preparation.
- Facilitates scientific and data exchange for both Company and competitor data and collects meaningful insights.
- Staffs congress exhibit booth as applicable.
Scientific Insights:
- Gathers feedback, data, or information during routine activities that can help the Company better comprehend medical or scientific needs, priorities, or concerns of healthcare practitioners and/or patients.
Inclusive Mindset and Behavior:
- Demonstrates eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment.
- Leads by example and serves as a role model for creating, leading and retaining a diverse and inclusive workforce.
Requirements:
- PhD, PharmD, DNP, or MD or equivalent.
- Clinical (patient care) or research experience in assigned therapeutic areas beyond that obtained in the terminal degree program.
- Proven competence and a minimum of 3 years of relevant therapeutic area experience.
- Ability to conduct doctoral-level discussions with key external stakeholders.
- Dedication to scientific excellence with a strong focus on scientific education and dialogue.
- Business and market knowledge.
- Excellent stakeholder management, communication, and networking skills.
- A thorough comprehension of local/regional regulatory agencies and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers.
- Ability to organize, prioritize, and work effectively in a constantly changing environment.
- Ensuring accountability to drive an inclusive culture.
- Strengthening the foundational elements of diversity.
- Consistent adherence to field and corporate policies, including field standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
- Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access).
- Desire to contribute to an environment of belonging, engagement, equity, and empowerment by:
- Working to transform the environment, culture, and business landscape.
- Leveraging diversity and inclusion to increase competitive advantage, per global diversity and inclusion strategy.
Advantages:
- Clinical research experience.
- Demonstrated record of scientific/medical publication.
- Relevant therapeutic area experience.
- Field-based medical experience.
Current Contingent Workers apply
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