Medical Affairs Specialist

Integra LifeSciences Corporation

Princeton (NJ)

On-site

USD 71,000 - 98,000

Full time

8 days ago
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Job summary

Integra LifeSciences Corporation in Princeton, New Jersey, is seeking a Medical Affairs Specialist to provide scientific and clinical support across the Tissue Reconstruction portfolio. The role involves evaluating literature, supporting medical information materials, and coordinating publication activities with cross-functional teams.

You will work under the Medical Director, Medical Affairs, contributing to evidence generation and regulatory-compliant communications while developing toward a

Qualifications

  • Advanced clinical or health sciences degree preferred (PharmD, PhD, DNP, PA-C, NP, RN or other relevant degree).
  • 0-3 years of experience in Medical Affairs, Clinical Affairs, Scientific Affairs, or related roles.
  • Experience in medical devices, biologics, wound care, or related therapeutic areas preferred.
  • Ability to critically evaluate clinical literature and scientific data.
  • Experience supporting scientific communications, publications, medical education, or medical information activities preferred.
  • Familiarity with medical device regulatory and compliance environments.

Responsibilities

  • Provide scientific and medical support for internal stakeholders regarding products, technologies, and therapeutic areas.
  • Assist in evaluating and summarizing scientific literature and clinical evidence under Medical Affairs leadership.
  • Support development and review of medical information materials and publications.
  • Coordinate and support evidence-generation activities and publication support.

Skills

Literature review
Scientific knowledge
Communication skills
Project management
Analytical thinking

Education

Advanced health sciences degree

Tools

CRM systems

Job description

## Medical Affairs SpecialistApply: US-NJ-Princeton-100-Headquarters: Full time: Posted Today: JR-6677Changing lives. Building Careers.Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.**SUMMARY DESCRIPTION**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.**SUPERVISION RECEIVED**Reports to Medical Director, Medical Affairs**SUPERVISION EXERCISED**None**KEY RESPONSIBILITIES****Scientific and Medical Support*** **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.**Medical Communications and Information*** 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.**Evidence Generation and Clinical Support*** 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.**Cross-Functional Collaboration*** 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.**Operational Excellence*** 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.**DESIRED MINIMUM QUALIFICATIONS*** 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.* Experience in medical devices, biologics, wound care, regenerative medicine, tissue reconstruction, surgical technologies, or related therapeutic areas preferred.* Demonstrated ability to critically evaluate clinical literature and scientific data.* Experience supporting scientific communications, publications, medical education, or medical information activities preferred.* Familiarity with medical device regulatory and compliance environments.**TECHNICAL COMPETENCIES*** 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.**Travel Requirements*** Limited travel (up to **10%**) for internal meetings, training programs, scientific congresses, and business-related activities. Travel may include weekend days.**PHYSICAL REQUIREMENTS**The physical requirements listed in this section include, but are not limited to, the motor/physical abilities and skills required of this position to successfully perform the essential duties and responsibilities of the role. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.Must be able and willing to travel up to 5-10% of work time. While performing the essential duties and responsibilities of the position, the employee must frequently sit, stand, drive, listen, speak, utilize electronic communication devices, and travel by automobile and air transportation.**ADVERSE WORKING CONDITIONS**The adverse working conditions listed in this section include, but are not limited to, those environmental conditions which the employee may be exposed to while performing the essential duties and responsibilities of the position.Occasional exposure to healthcare settings may require adherence to institutional safety protocols, infection prevention procedures, and personal protective equipment requirements.# **SELECTION GUIDELINES**Formal applications, rating of education and experience; oral interview and reference check; job-related assessments may be required.# **DISCLAIMER**The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.Salary Pay Range:$71,300.00 - $97,750.00 USD Salary
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