Medical Affairs Specialist

Integra LifeSciences•Princeton, NJ

7d•$71,300 - $97,750•Hybrid

About The Position

Medical Affairs Specialist is a foundational Medical Affairs role that provides scientific, clinical, and operational support across the Tissue Reconstruction portfolio. Under the guidance of experienced Medical Affairs professionals, the position supports scientific communications, medical information activities, scientific education material development, publication support, medical review processes, including promotional material review, and the communication of clinical evidence. The role collaborates across functions to ensure medical accuracy and effective execution of Medical Affairs initiatives while focusing on operational excellence, capability development, and serving as a developmental pathway toward a field-based Medical Science Liaison (MSL) role.

Requirements

Advanced clinical or health sciences degree preferred (PharmD, PhD, DNP, PA-C, NP, RN or other relevant health sciences degree) or a master's degree in a relevant scientific discipline.
0-3 years of experience in Medical Affairs, Clinical Affairs, Scientific Affairs, Clinical Research, healthcare, or related industry roles.
Demonstrated ability to critically evaluate clinical literature and scientific data.
Familiarity with medical device regulatory and compliance environments.
Strong scientific and clinical knowledge.
Excellent literature evaluation and critical thinking skills.
Strong written, verbal, and presentation communication abilities.
Ability to communicate scientific concepts effectively to diverse internal audiences.
Strong organizational and project management capabilities.
Ability to work independently and collaboratively in a cross-functional environment.
Analytical mindset with strong problem-solving skills.
High level of professionalism, integrity, and attention to detail.

Nice To Haves

Experience in medical devices, biologics, wound care, regenerative medicine, tissue reconstruction, surgical technologies, or related therapeutic areas preferred.
Experience supporting scientific communications, publications, medical education, or medical information activities preferred.

Responsibilities

Assist as a scientific and medical resource for internal stakeholders regarding assigned products, technologies, and therapeutic areas.
Support the evaluation and summary of scientific literature, clinical evidence, and competitive intelligence under the guidance of Medical Affairs leadership.
Monitor developments in tissue reconstruction, regenerative medicine, wound care, and related therapeutic areas to support Medical Affairs activities.
Assist in translating scientific findings into practical insights for internal stakeholders.
Support the development and review of medical information materials, scientific communications, scientific education materials, and product-related documentation.
Support medical review processes, including the review of promotional and non-promotional materials, to ensure medical accuracy and scientific consistency.
Assist in the preparation and review of abstracts, posters, manuscripts, presentations, and publication materials.
Support responses to medical information requests and scientific inquiries.
Support evidence-generation activities through literature reviews, publication support activities, and documentation coordination under the guidance of Medical Affairs leadership.
Support the review of clinical evidence to assist Medical Affairs planning and communication activities.
Assist with the compilation and organization of scientific and clinical information to support internal decision-making.
Provide scientific support for research initiatives and post-market evidence assessment activities.
Collaborate with Regulatory Affairs, Clinical Affairs, Research & Development, Marketing, Professional Education, Market Access, and Commercial teams.
Participate in cross-functional projects and provide scientific input on assigned initiatives.
Support the development of scientific training and educational materials for internal stakeholders.
Support cross-functional teams by providing medical and scientific input on assigned projects and initiatives.
Support execution of Medical Affairs projects, timelines, deliverables, medical information processes, and Medical Affairs operational systems and databases.
Maintain Medical Affairs documentation, databases, CRM systems, and associated records to support departmental activities and compliance requirements.
Maintain knowledge of applicable medical device regulations, compliance requirements, and industry standards.
Ensure activities are conducted in accordance with company policies and applicable legal, regulatory, and ethical requirements.
Effectively manage multiple priorities and projects in a collaborative environment.