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Scientist Physician, Medical Device

Clinchoice
ClinChoice
5-7 years
Not Disclosed
10 Jan. 15, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist Physician – Medical Affairs (Medical Devices) | Remote – US

Location: United States (Remote)
Department: Medical Affairs
Employment Type: Full-Time
Experience Required: 5–7 Years
Educational Qualification: MD (Cardiology)


Job Overview

We are seeking a Specialist Physician – Medical Affairs with expertise in medical devices to join our global team. The role is responsible for ensuring medical and scientific accuracy of regulatory, promotional, and scientific materials, supporting clinical and commercial teams, and providing medical expertise across the product lifecycle. This position interacts with internal stakeholders (e.g., Clinical R&D, Safety, Medical Affairs) and external stakeholders, contributing to overall medical strategy and product success.


Key Responsibilities

Medical Expertise & Strategy

  • Provide medical and scientific support across regulated medical device products.

  • Participate in literature reviews and interpretation of clinical study data in collaboration with regional and global Medical Affairs teams.

  • Identify and address potential medical issues, implementing risk-management strategies.

  • Contribute to the development and execution of medical strategies for assigned devices.

Regulatory & Scientific Content

  • Prepare, review, and ensure accuracy of regulatory, promotional, and scientific materials.

  • Support medical content development for congresses, symposia, and advisory boards.

  • Review and revise materials in response to published literature, media coverage, or new medical discoveries.

  • Develop and review medical training programs for new hires and ongoing education.

  • Provide input on product information manuals, FAQs, labeling, and packaging components.

Cross-Functional Collaboration

  • Serve as a medical resource for cross-functional teams to ensure accuracy in promotional and non-promotional content.

  • Support preparation of safety reports, regulatory submissions, PSURs, CCDS, and annual reports.

  • Mentor junior team members, providing domain knowledge and functional training.

Quality & Compliance

  • Ensure timely delivery of high-quality, error-free deliverables in line with project SLAs.

  • Perform functional reviews of team outputs for accuracy and compliance.

  • Maintain compliance with QMS/ISMS/PIMS policies, security protocols, and training requirements.

  • Identify potential risks and escalate issues proactively.


Required Qualifications

  • MD in Cardiology aligned with project/business needs.

  • 5–7 years of relevant experience in medical affairs, clinical support, or medical device-related domains.

  • Strong knowledge of medical device regulations, clinical data interpretation, and risk management.

  • Excellent communication, mentoring, and cross-functional collaboration skills.

  • Ability to work independently and manage multiple deliverables with high quality and compliance standards.


Why Join Us

  • Be part of a global medical affairs team supporting innovative medical devices.

  • Engage with internal and external stakeholders to shape clinical, regulatory, and promotional strategies.

  • Collaborate in a remote-friendly environment with opportunities for professional growth.

  • Contribute to high-impact projects ensuring safety, compliance, and scientific integrity.


Apply now to join our team as a Specialist Physician – Medical Affairs and help drive medical excellence in medical device innovation.