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QUALIFICATIONS
Required:
- Advanced degree (e.g., PharmD, MSc, MD, PhD)
- At least 4 years of experience in a biopharmaceutical, biotech, or CRO setting
- Demonstrated experience in developing and executing medical strategy and tactics
- Proven track record of executing medical-affairs activities such as advisory boards, medical education programs, KOL engagement, and scientific publications
- Demonstrated ability to build and maintain relationships with cross-functional colleagues and external stakeholders
- Solid understanding of drug development, clinical research, and regulatory requirements
- Strong written and verbal communication skills for both scientific and non-scientific audiences
Preferred:
- PharmD or PhD in a relevant scientific field.
- Experience supporting medical, clinical, or regulatory activities in a biopharmaceutical or medical-device company.
- Familiarity with device/drug combinations, specialty pharmacy, home infusion, payer environments, and therapeutic areas such as oncology or rare disease
Skills & Competencies:
- Knowledge of drug-development processes
- Strong organizational and operational skills to keep medical-affairs activities running smoothly
- Ability to collaborate effectively with colleagues and external partners
- Business and scientific acumen
- Creative problem-solving skills
Physical Requirements:
- Ability to remain stationary for extended periods and operate standard office equipment
- Ability to set up conference booths and support congress activities
- Ability to travel up to 20% domestically and internationally
RESPONSIBILITIES
- Support biopharmaceutical partner drug launches via KOL engagement, conference attendance, publication support, and other medical-affairs activities
- Assist in implementing Enable Injections’ business-development and corporate strategies by providing scientific input at conferences, partner meetings, and business-development events
- Deliver external and internal educational/product training under the direction of senior team members
- Provide input on clinical-development plans and collaborate with partners, reporting recommendations to senior leadership
- Coordinate with internal teams—including Product Development, Operations, Regulatory Affairs, Marketing, Program Management, and others—to integrate medical-affairs activities into overall product strategy and lifecycle management
- Cultivate and maintain relationships with KOLs, healthcare professionals, and scientific societies
- Contribute to publication planning and the preparation of scientific manuscripts, ensuring compliance with regulatory and ethical guidelines
- Monitor scientific advancements, market trends, and competitive landscape to provide insights to senior leadership
- Prepare scientific booth materials, coordinate medical presence, and manage symposia at global and regional congresses
- Provide accurate, timely responses to unsolicited medical information requests from healthcare providers
- Contribute to non-interventional study design, registries, and real-world data initiatives
- Partner with Regulatory, Clinical Development, Commercial, Market Access, and other partners to ensure medical alignment
- Ensure all medical activities are conducted in line with industry codes, regulations, and internal SOPs
- Maintain organizational systems, processes, and documentation to ensure efficient execution of medical-affairs initiatives
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