Clinical Researcher

A confidential healthcare technology and analytics organization is hiring a Clinical Researcher to develop evidence-based insights for healthcare product evaluation and procurement decisions. The role researches and synthesizes clinical literature and real-world evidence, assesses study quality and product safety, and translates findings into structured insights for decision-support initiatives.

Responsibilities

Conduct systematic literature reviews and evidence searches utilizing resources such as PubMed, Embase, Cochrane Library, FDA MAUDE, clinical registries, and other research databases

Evaluate and synthesize clinical studies, real-world evidence, and post-market surveillance data related to medical devices, implants, and clinical consumables

Assess study quality and strength of evidence using established research methodologies and evidence-rating frameworks

Monitor emerging clinical research, specialty-specific literature, and healthcare trends that may impact product performance, utilization, or risk

Translate clinical findings into structured and standardized formats to support evidence-scoring methodologies and decision-support tools

Maintain accurate source documentation, citations, and research audit trails to ensure transparency and traceability

Track product recalls, adverse events, safety alerts, and post-market surveillance trends relevant to healthcare products and supply risk

Support the development and maintenance of evidence repositories, datasets, and research documentation

Partner with product, analytics, and data teams to support evidence quality, confidence, and risk-scoring methodologies

Prepare research findings, evidence summaries, and supporting analyses for internal stakeholders

Contribute to customer-facing deliverables, including research briefs, evidence summaries, white papers, and educational materials

Present complex clinical and scientific information in a clear and understandable manner for both clinical and non-clinical audiences

Perform other duties and special projects as assigned

Preferred

Master's degree in Public Health, Health Sciences, Nursing, Library Science, or a related discipline

Clinical credentials or healthcare background such as RN, PharmD, MPH, or an equivalent credential

Experience with orthopedic implants, medical devices, healthcare technologies, or hospital supply chain environments

Experience supporting value analysis committees, product evaluation programs, sourcing initiatives, or GPO-related activities

Familiarity with regulatory and post-market surveillance resources, including FDA MAUDE and clinical registries

Experience working with health technology assessment organizations, healthcare consulting firms, medical device manufacturers, or evidence-based research teams

Master’s Degree in Public Health

Master’s Degree in Health Sciences

Master’s Degree in Nursing

Master’s Degree in Library Science

Registered Nurse (RN)

Doctor of Pharmacy (PharmD)

Master of Public Health (MPH)

Orthopedic Implants

Medical Devices

Healthcare Technologies

Hospital Supply Chain

Value Analysis Committees

Product Evaluation Programs

Sourcing Initiatives

Group Purchasing Organizations (GPOs)

Regulatory Resources

Clinical Registries

Healthcare Consulting

Medical Device Manufacturing

Evidence-Based Research

Benefits

Fully remote work environment.

Gain exposure to medical devices, healthcare innovation, and emerging clinical evidence.

Company

Hiring Solutions

0-1 employees

Qualifications

Bachelor's degree in Life Sciences, Nursing, Public Health, Health Informatics, or a related field

Minimum of 2 years of experience in clinical research, literature review, health technology assessment (HTA), medical writing, evidence-based medicine, or a related discipline

Knowledge of systematic review methodologies, literature search strategies, and evidence appraisal techniques

Familiarity with clinical research design, biostatistics concepts, and evidence grading frameworks

Experience interpreting, analyzing, and summarizing complex clinical and scientific information

Strong written communication skills with the ability to communicate technical findings to diverse audiences

Experience using spreadsheets, databases, structured datasets, or similar research tools

Strong organizational and analytical skills with attention to detail

Clinical literature databases and research platforms (PubMed, Embase, Cochrane Library)

Systematic review methodologies and evidence appraisal techniques

Clinical research evaluation and evidence-grading frameworks

FDA MAUDE and other post-market surveillance resources

Spreadsheet and structured data analysis tools

Basic SQL and data-query concepts

Research documentation and citation management systems

Microsoft Office Suite

Master's degree in Public Health, Health Sciences, Nursing, Library Science, or a related discipline

Clinical credentials or healthcare background such as RN, PharmD, MPH, or an equivalent credential

Experience with orthopedic implants, medical devices, healthcare technologies, or hospital supply chain environments

Experience supporting value analysis committees, product evaluation programs, sourcing initiatives, or GPO-related activities

Familiarity with regulatory and post-market surveillance resources, including FDA MAUDE and clinical registries

Experience working with health technology assessment organizations, healthcare consulting firms, medical device manufacturers, or evidence-based research teams

Minimum of 2 years of experience in clinical research, literature review, health technology assessment (HTA), medical writing, evidence-based medicine, or a related discipline.

Required skills

Systematic Literature Review, Literature Search Strategies, Evidence Appraisal, Clinical Research Design, Biostatistics, Evidence-Grading Frameworks, Health Technology Assessment, PubMed, Embase, Cochrane Library, FDA MAUDE, SQL

Experience

2+ years