Clinical Strategy Lead

Convatec

Clinical Strategy Lead for Advanced Wound Care at Convatec. Involved in clinical study design and evidence generation strategies with cross-functional collaboration.

Posted 7/1/2026full-timeRemote • District of Columbia, Illinois, Massachusetts, New York • 🇺🇸 United StatesSenior💰 $124,800 - $195,000 per yearWebsite

About the role

Key responsibilities & impact

Act as a clinical strategist for our Advanced Wound Care Medical and Clinical Affairs team, with a special focus on emerging Advanced Wound Care technologies
Play a lead role in clinical study design, including regulatory approvals, statistical analysis plan, and budget
Close collaboration with Global Medical Education and Key Opinion Leader Management colleagues and Business Development and Marketing teams through interactions with key opinion leaders, healthcare providers, and regulatory bodies to analyze and identify unmet needs in our field
Work closely with the clinical operations colleagues to translate business strategies to actionable clinical study protocols and retrospective data generation plans
Analyze data output from clinical studies and other evidence generation activities and distill these into a cohesive "story" to be presented when needed
Play a proactive role in putting together publications and evidence communication in close collaboration with the medical writing team
Act as an educator and role model for colleagues outside of medical affairs
Support all our general medical affairs activities, including, but not limited to new product development, evidence generation and review, risk management, and other activities as needed
Act as a subject matter expert in the product line

Requirements

What you’ll need

Bachelor’s degree or higher degree in Medicine, Life Sciences, Allied Health, Pharmacy, or Nursing
Advanced degree (MD, PhD MSN, DNP) preferred
Clinical experience or specialty knowledge in wound care preferred
At least 3 years’ experience in the medical device or pharmaceutical industry in positions of increasing responsibility
Strong understanding of clinical research, including literature reviews, protocol development, general study execution, and statistical analysis
Experience in clinical study design in an industry or academic setting
Understanding of the medical device industry: product development, pre-clinical, clinical, quality, marketing, and regulatory components
Experience with regulatory requirements for clinical studies in the US and EU is highly desirable
Strong computer skills and high level of proficiency of Microsoft Office
Ability to communicate fluently in English

Benefits

Comp & perks

health benefits for individuals, families, and domestic partners, including medical, prescription drug, dental, and vision coverage
paid vacation
holidays
community service days
sick time
paid caregiver/parental leave
medical leave
retirement savings plan with company match

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical ResearchProtocol DevelopmentData AnalysisLiterature ReviewEvidence Generation

Soft Skills

CommunicationCollaborationEducation

Certifications

Bachelor’s DegreeAdvanced Degree (MD, PhD, MSN, DNP)