Associate Director, Clinical Research & Real-World Evidence

About Sequel Sequel, headquartered in Manchester, New Hampshire, is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. Sequel’s approach is to look at diabetes management holistically to advance systems that make living with diabetes simpler and easier for all. Sequel’s flagship product, the twiist Automated Insulin Delivery (AID) System, launched in July 2025 for people with type 1 diabetes providing them with personalized diabetes management. 

Job Overview

The Associate Director, Clinical Research and Real-World Evidence is a hands-on scientific contributor who drives and executes clinical research, real-world evidence (RWE), biostatistical planning and interpretation, and other evidence-generation activities across Sequel Med Tech's product portfolio, including the twiist Automated Insulin Delivery (AID) System. Working closely with the Chief Medical Officer and cross-functional partners, this role translates clinical and business questions into rigorous, feasible research plans and helps generate evidence to support product development, regulatory activities, reimbursement, clinical adoption, and scientific dissemination.

The ideal candidate can independently contribute to protocol development, endpoint selection, statistical analysis plans, interpretation of clinical and real-world data, and study execution, while working closely with the CMO and other subject-matter experts on broader evidence strategy. Experience supporting medical device regulatory submissions or working within a regulated environment is preferred. The role will collaborate with internal teams and external investigators, academic research organizations, analytics partners, and other research vendors.

Job Responsibilities and Essential Duties

Real-World Evidence & Biostatistics: Design and support RWE studies; contribute to research questions, endpoint definitions, analysis plans, data-quality review, interpretation, and communication of results; partner effectively with internal or external statisticians and data scientists.

Study Design & Regulatory Support: Lead the development of study protocols and study concepts for company-sponsored, collaborative, post-market, and pivotal studies, including objectives, populations, comparators, endpoints, sample-size considerations, and analysis approaches; develop clinical evidence for regulatory briefing materials, submissions, and responses.

Clinical Research Execution: Drive study start-up and execution, including protocol and case-report-form development, vendor and investigator coordination, data review, issue resolution, analysis, and interpretation across company-sponsored studies, investigator-initiated studies, and special-population research.

Evidence Planning: Partner with the CMO to identify evidence gaps and research priorities and drive an integrated evidence-generation plan spanning clinical studies, real-world evidence, publications, and external collaborations.

Clinical Evidence Development: Develop clinical evidence materials, including competitive data comparisons, dossiers, evidence summaries, and scientific narratives supporting regulatory, reimbursement, product adoption, medical education, publications, and OUS opportunities.

Payer / Market Access: Develop clinical and economic evidence summaries supporting reimbursement, payer engagements, and market-access activities.

Publications & Scientific Communications: Support scientific publications, abstracts, posters, congress presentations, and dissemination of clinical and real-world evidence.

Medical Affairs Strategy: Contribute to the execution of the Medical Affairs strategy and evidence roadmap, supporting clinical adoption, reimbursement, patient outcomes, and future growth objectives.

Medical Education & Scientific Engagement: Serve as a scientific resource across the product portfolio; support advisory boards, congress activities, medical education programs, and engagement with healthcare professionals, investigators, and key opinion leaders.

Medical Safety: Participate in hazard analysis reviews, adverse-event and complaint evaluations for Sequel owned product, post-market safety activities, and related investigations.

Minimum Requirements

Education: Advanced degree in biostatistics, epidemiology, health outcomes research, clinical research, public health, or a relevant scientific or healthcare discipline (e.g., PhD, ScD, DrPH, PharmD, MD, or MS).

Experience: 5+ years of relevant experience in clinical research, RWE, biostatistics, epidemiology, medical device or pharmaceutical evidence generation, or a related field; a doctoral degree may substitute for a portion of professional experience.

Experience in a regulated medical device, pharmaceutical, biotechnology, academic research, contract research, or health-data environment; direct experience supporting regulatory activities is preferred.

Required Knowledge, Skills and Abilities

Strong knowledge of clinical study design, observational research, registry studies, and real-world evidence methods.

Applied understanding of biostatistical principles, including endpoint selection, sample-size and power considerations, longitudinal and repeated-measures data, missing data, confounding, bias mitigation, and interpretation of clinical and real-world analyses.

Ability to develop or critically review protocols, statistical analysis plans, tables and figures, and study reports, and to collaborate effectively with statisticians and programmers.

Experience supporting clinical research execution, including investigator or vendor collaboration, data review, and interpretation of study findings.

Familiarity with FDA expectations, Good Clinical Practice, and clinical evidence requirements for regulated products; medical device experience is preferred.

Knowledge of clinical research and regulatory requirements outside the U.S., including experience supporting global or international evidence-generation activities, is preferred.

Experience preparing abstracts, posters, manuscripts, evidence summaries, or other scientific communications.

Knowledge of diabetes management, insulin therapy, continuous glucose monitoring, and Automated Insulin Delivery systems is preferred.

Strong scientific writing, communication, project management, and cross-functional collaboration skills.

Ability to work independently, manage multiple research activities, and translate evidence into clear scientific, clinical and business insights.

Sequel Med Tech provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. At Sequel, we believe that when you thrive, we thrive. That’s why our benefits package is designed to support you from day one. You’ll be automatically enrolled in our 401k plan, featuring a 6% company match and 100% immediate vesting. We’re committed to your well-being and understand the unique needs of employees and families living with diabetes, so we offer capped out-of-pocket insulin costs and GLP-1 coverage across all plans. You’ll have access to a variety of Meritain health insurance plans to suit your needs and can also take advantage of Flexible Spending Accounts (FSAs) or Health Savings Account (HSA). Our comprehensive benefits package includes vision and dental coverage, plus voluntary options such as long-term disability, accident, critical illness, hospital indemnity, and even discounts for pet care. In addition, we provide employer-paid short-term disability and life insurance for extra peace of mind. We know the importance of taking time to rest and recharge. That’s why Sequel offers flexible PTO, generous paid holidays, and Flex Time options to help you balance work and life when you need it most. Our team enjoys a culture built on hard work, fun, and genuine support. At Sequel, you’re not just starting a job, you’re building a rewarding career and a brighter future. Join us, and let’s thrive together! Environmental/Safety/Physical Work Conditions Ensures environmental consciousness and safe practices are exhibited in decisions Use of computer and telephone equipment and other related office accessories/devices to complete assignments May work extended hours during peak business cycles Physical requirements such as lifting specific weights Some travelling is expected

Advanced degree in biostatistics, epidemiology, health outcomes, clinical research, public health, or related field; 5+ years relevant experience in clinical research, RWE, biostatistics, or medical device/pharmaceutical evidence generation; strong knowledge of clinical study design and biostatistics.

Key Responsibilities

• designing research studies
• analyzing clinical data
• supporting regulatory submissions

Job Details

• Category: Research and Development (R&D)
• Seniority: Senior Level
• Commitment: Full Time
• Workplace: Remote — Manchester, New Hampshire, United States
• Salary: USD 170,000 – 220,000 / year
• Languages: English

Benefits

• 401k matching
• Generous paid time off
• Retirement plan

About Sequel Med Tech

A company developing transformative drug-delivery advancements for diabetes management. — Industry: Healthcare