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Associate Director, Clinical Research & Real-World Evidence

Sequel Med Tech · United States · US

Clinical Research
Remote
physician
Pharmacist
Dentist
Demand82
Career growth84
Healthcare fit88
Remote potential45
Salary band
USD 170k – 220k
5-year outlook
Senior clinical research and RWE roles in medical device and digital health typically offer competitive compensation, with exact pay depending on location, experience, and scope. Growth should be supported by increasing demand for evidence generation, reimbursement support, and real-world data across medtech.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-25

Intelligence details

Flexible work details

Side income
Classified as side-income friendly
Engagement type
Contract
Hours
Variable hours
Eligible countries
United States
Profession fit
physician, Pharmacist, Dentist
Rate period
Annual

Why this was classified this way

  • contract

Listing via Himalayas.

Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.

Why this is worth applying to

Worth applying for clinicians with prior clinical research, RWE, biostatistics, regulatory evidence, or medical affairs experience who want a senior industry evidence-generation role. Clinicians without industry research or medtech evidence experience may find the bar high.

Who should apply

Physicians, pharmacists, nurses, and allied health professionals with CRO, pharma, device, or health-system research experience; especially those with protocol development, real-world evidence, publications, regulatory submissions, or medical affairs exposure.

CV angle

Frame real clinical training and practice as the foundation for endpoint selection, data interpretation, and clinical adoption, then emphasize concrete research deliverables such as protocols, analysis plans, publications, regulatory evidence, cross-functional collaborations, and vendor/investigator coordination. Do not claim industry RWE or medtech regulatory experience unless genuinely held.

Skills to highlight

  • Clinical research study design
  • Real-world evidence generation
  • Protocol and endpoint development
  • Biostatistical planning and data interpretation
  • Medical device regulatory evidence support
  • Scientific publications and communications
  • Cross-functional collaboration with CMO, investigators, and vendors
  • Payer/market access evidence summaries

Role summary

A senior, hands-on clinical research and real-world evidence role at a medical device company, focused on designing studies, supporting biostatistics and regulatory evidence, generating payer-relevant evidence, and disseminating scientific findings for an automated insulin delivery system.

We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.