Clinical and Medical Research Specialist

Sequel Med Tech

. Manage operational activities across Sequel’s research and evidence-generation portfolio .

Posted 11/4/2026full-timeUnited StatesMid-LevelSenior💰 $100,000 - $110,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research operations, including project planning, data management, and compliance with regulatory standards. Proficient in coordinating cross-functional teams and maintaining organized, audit-ready documentation in a regulated environment.

Highest-signal resume keywords

Clinical Research ManagementProject Planning and ExecutionData Management and AnalysisRegulatory Compliance KnowledgeStrong Organizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical TrialsEpidemiologic StudiesData AnalysisSOP ManagementMicrosoft ExcelResearch DocumentationProject Management SystemsGood Clinical PracticeMedical Device ResearchPost-Market Research

Soft Skills

Strong Attention to DetailEffective CommunicationSound JudgmentIndependent Work CapabilityOrganizational Skills

Industry Keywords

Health ScienceLife SciencePublic HealthBiotechCRO EnvironmentDigital HealthDevice-Generated DataResearch CollaborationsParticipant SafetyFDA Regulations

About the role

Key responsibilities & impact

Manage operational activities across Sequel’s research and evidence-generation portfolio
Develop, maintain, and interpret project plans, study and enrollment trackers, timelines, status reports, decision logs, and source-of-truth materials
Assess project status, delays, dependencies, and research execution risks; recommend mitigation actions
Lead research start-up and execution activities across internal stakeholders, investigators, research sites, vendors, and external partners
Manage CRO relationships and day-to-day operational execution of assigned CRO-led studies
Coordinate investigator-initiated and external research collaborations
Work with external product development and manufacturing partners, including DEKA and Millyard, on research-related needs
Ensure collection, cleaning, organization, reconciliation, and documentation of research data
Maintain analysis-ready datasets, data dictionaries, supporting documentation, tables, graphs, dashboards, and basic descriptive summaries
Assess research and data requests, evaluate feasibility, identify approval requirements, prioritize work, and recommend timelines and deliverables
Manage research-related SOPs, work instructions, templates, and supporting documentation
Manage project meetings, action items, vendor and investigator coordination, budgets, forecasts, invoices, agreements, and project documentation
Maintain accurate, organized, and audit-ready research records
Evaluate and escalate issues affecting research conduct, participant safety, data integrity, compliance, timelines, or evidence quality

Requirements

What you’ll need

Bachelor’s degree in health science, life science, public health, epidemiology, clinical research, data science or related discipline
3+ years of experience supporting clinical, medical, epidemiologic, or related research programs
Experience within a medical device, pharmaceutical, biotech, or CRO environment
Experience supporting medical device research and working within a regulated industry environment is required
Experience with medical device, diabetes, digital health, or device-generated data research is preferred
Familiarity with Good Clinical Practice
Experience with clinical trials, post-market studies, observational or epidemiologic studies, real-world evidence or secondary data analysis
Experience working with research data, SOPs, external research organizations, CROs, investigators, sites, vendors, or scientific collaborators
Strong organizational and project-management skills
Proficiency with Microsoft Excel and research and/or project-management systems
Strong attention to detail and analytical skills
Working knowledge of clinical and research operations, including IRB/ethics submissions, informed consent, study documentation, post-market research, and applicable FDA, Good Clinical Practice, and other research requirements and processes
Strong written and verbal communication skills
Ability to develop and maintain organized, audit-ready research documentation, procedures, and standardized workflows
Ability to appropriately handle confidential information, including protected health information (PHI) and sensitive research data
Sound judgment regarding confidentiality, research documentation, data handling, issue escalation, and role authority
Ability to work independently and seek advice when necessary
Commitment to accurate, compliant, organized, and audit-ready research practices
Ability and willingness to work regularly from the Manchester, NH office and travel as required

Benefits

Comp & perks

401k plan with a 6% company match and 100% immediate vesting
Capped out-of-pocket insulin costs
GLP-1 coverage across all plans
Meritain health insurance plans
Flexible Spending Accounts (FSAs)
Health Savings Account (HSA)
Vision and dental coverage
Voluntary long-term disability, accident, critical illness, and hospital indemnity coverage
Discounts for pet care
Employer-paid short-term disability and life insurance
Flexible PTO
Generous paid holidays
Flex Time options