Manager, Medical Affairs – MedTech Surgery
OneTrust
full-time
Posted on:
Location Type: Hybrid
Location: Cincinnati • Ohio • United States
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Salary
💰 $117,000 - $201,250 per year
About the role
- Serve as a strategic and scientific partner across the product lifecycle, contributing to evidence generation, scientific communications, and medical strategy for key products within the Surgery portfolio.
- Scaling the impact, efficiency, and output of medical writing using internal expertise, external agencies, and emerging AI technologies.
- Collaborate closely with cross functional partners in R&D, Clinical Research, Regulatory Affairs, Medical Safety, Quality, Marketing, and Professional Education to ensure scientific accuracy, product safety, and robust evidence generation supporting global commercialization.
- Engage with key opinion leaders, investigators, and clinical partners to strengthen external scientific collaboration.
- Stay current with emerging literature and competitive intelligence to inform research priorities, evidence strategy, and product positioning.
- Contribute to early product introduction, including clinical insights for launches, training, and procedural optimization.
- Lead and scale scientific communications, including manuscripts, abstracts, posters, and congress materials.
- Manage and expand external medical writing agencies, ensuring quality, scientific rigor, and high return on investment.
- Oversee publication planning, timeline management, and cross functional review/approval processes.
- Conduct Medical Information Requests (MIRs), copy review, product claim assessments, and scientific accuracy checks.
Requirements
- Bachelor’s degree in life sciences, biomedical engineering, nursing, pharmacy, or related field is required.
- Advanced degree (MS, PhD, MD, PharmD, MBA) is strongly preferred.
- A minimum of 2+ years of industry experience in Medical Affairs, Clinical Affairs, Scientific Communications, or related functions within a medical device or highly regulated health tech environment is required.
- Hands-on experience in clinical or operating room settings (physician, nurse, or scientist) is required.
- Proven track record in scientific writing (manuscripts, abstracts, posters) and presenting at scientific conferences is required.
- Strong analytical skills with experience interpreting clinical or preclinical data is required.
- Demonstrated ability to manage multiple projects, timelines, and cross-functional stakeholders is required.
- Experience in leading or scaling medical writing functions, including agency management, is preferred.
- Familiarity with clinical trial design, biostatistics, and evidence-generation strategies is preferred.
- Strong understanding of regulatory pathways and product development processes in the medical device sector is preferred.
- Leadership potential and a demonstrated history of increasing responsibility.
Benefits
- Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
- Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
scientific writingclinical trial designbiostatisticsevidence-generation strategiesdata interpretationpublication planningmedical information requestscopy reviewproduct claim assessmentsproject management
Soft Skills
analytical skillscollaborationleadershipcommunicationorganizational skillsstakeholder managementstrategic thinkingtime managementproblem-solvingadaptability
Certifications
Bachelor’s degree in life sciencesMSPhDMDPharmDMBA