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Boston Scientific · 1 day ago

Senior Clinical Research Specialist

Minnetonka, MN

Full-time

Hybrid

Mid, Senior Level

$83K/yr - $157K/yr

4+ years exp

Boston Scientific is a leader in medical science, committed to solving important health industry challenges. The Senior Clinical Research Specialist will support key commercialized products by developing and executing clinical research activities while collaborating cross-functionally to ensure the appropriateness of research scope.

Health CareMedicalMedical Device

No H1B

Responsibilities

Support strategic growth of our team’s Real-World Evidence (RWE) capabilities and demonstrate ROI in the use of these new clinical data sources

Plan and execute feasibility and analysis of BSC Urology RWE studies programmatically utilizing data science techniques and contribute to post-market documentation, publications, and other documents as needed

Design studies utilizing administrative claims, Electronic Health Records (EHR), and other RWE data sources by applying clinical research methodologies (e.g., research question development, population inclusion/exclusion, reduction of bias, etc.)

Develop coding definitions utilizing reimbursement code sets (ICD-10-CM, ICD-10-PCS, CPT, etc.) and medical terminologies (SNOMED, LOINC, RxNorm, etc.) for populations, outcomes, and co-variates of interest in the Urology space

Collaborate cross-functionally with Clinical Strategy, Scientific Communication, Biostatistics, Medical Safety, Legal, and Compliance to design and run RWE studies

Manage internal and external project materials and timelines

Participate as a key team member on process development and improvement efforts to meet Urology VIP goals

Qualification

Clinical research methodologiesMedical coding systemsData analysis softwareReal World Evidence (RWE)Scientific writingTeam collaborationClear communication

Required

Minimum of a Bachelor's Degree in a related field and 4 years of related work experience (including data analytics, data management, health economics, medical affairs, clinical risk, clinical trial operations, clinical safety, quality assurance or regulatory affairs) or advanced degree (PhD, research-based MS, MD, RN/DVM) in a related field with 4+ years of related work experience

Expertise in leveraging medical coding systems and terminologies for research applications (ICD-9/10, CPT, SNOMED, LOINC, RxNorm, etc.)

Proven experience using Python, R, other software for exploring, structuring, and analyzing data sets, relational data modeling and querying expertise (SQL)

Ability to work in a team environment and possess clear, concise communication skills – both written and verbal

Preferred

Preferred medical device or clinical experience in Urology

Prior or current experience in retrospective research design with Real World data including claims data inclusive of Charge Master Data and/or Electronic Health Record (EHR) data

Proven scientific writing experience

Proven Physician-facing experience