Manager, Medical Information

Sequel Med Tech; Marlboro (MA); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

401k plan with 6% company match

Capped out-of-pocket insulin costs

Flexible PTO and generous paid holidays

Job summary

Sequel Med Tech is looking for a proficient medical communication specialist to handle inquiries, develop responses, and ensure compliance with regulatory standards. This role requires strong writing skills, a solid background in diabetes management, and 5+ years of experience in the medical device or pharmaceutical industry.

Join Sequel Med Tech in Marlboro, Massachusetts, and contribute to meaningful advancements in diabetes management. Enjoy a supportive environment and competitive benefits package, including medical insurance and flexible PTO.

Qualifications

• 5+ years of relevant industry experience in medical safety, pharmacovigilance, clinical research, or medical affairs.
• Strong understanding of the Medical, Legal, and Regulatory review process.
• Proven ability to partner across teams to align messaging.

Responsibilities

• Respond to verbal and written medical inquiries.
• Develop and maintain medical response documents.
• Coordinate with cross-functional teams to align medical communications.

Skills

Strong writing and editing skills

Knowledge of diabetes management

Ability to interpret clinical data

Experience in medical affairs

Education

Advanced degree in medicine, pharmacy, nursing, or life sciences

Job description

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.

Responsibilities

• Respond to verbal and written medical inquiries from internal and external customers.
• Preview, edit, and develop new standard medical response letters as needed; proactively develop medical response documents.
• Work closely with the Medical Affairs team, including medical directors, scientists, and the Chief Medical Officer, to gather and verify information.
• Coordinate with the marketing and public relations teams to align medical communications with broader company messaging.
• Perform meticulous proofreading and editing of all medical content to ensure grammatical accuracy, clarity, and consistency.
• Implement quality control measures to ensure all publications meet high standards of excellence.
• Manage the preparation and submission of medical content to the Medical, Legal, and Regulatory (MLR) and Scientific Material Review process.
• Perform medical accuracy review of promotional materials containing medical content.
• Ensure all content complies with regulatory and company standards before submission.
• Track and manage feedback from reviewers and implement necessary revisions.
• Develop, organize, and maintain the company’s repository of standard medical responses, FAQs, and reference materials.
• Ensure all medical inquiry resources are scientifically accurate, compliant, and aligned with regulatory and company standards.
• Provide ongoing updates and maintenance of these resources in response to new evidence, product updates, and regulatory guidance.
• Support Medical Affairs and cross‑functional teams by ensuring timely access to accurate, approved medical content for responding to inquiries.
• Ensure all communications comply with relevant regulatory requirements and ethical standards.
• Stay updated on industry guidelines and best practices for medical and scientific communication.
• Create unbranded presentations for Medical Affairs use.
• Translate scientific results for use in Medical Education presentations.
• Develop scientific summaries for distribution to HCPs.
• Compile and synthesize HCP insights to build scientific and education priorities.

Qualifications

• Education: Advanced degree in medicine, pharmacy, nursing, or life sciences (MD, PharmD, PhD, NP, PA, or equivalent).
• Experience: 5+ years of relevant industry experience in medical safety, pharmacovigilance, clinical research, or medical affairs.
• Experience in the medical device and/or pharmaceutical industry with exposure to post‑market surveillance and safety reporting.
• Strong writing and editing skills to prepare medical response letters, scientific summaries, and HCP‑facing content with accuracy and clarity.
• Strong understanding of diabetes management and familiarity with insulin pump therapy preferred.
• Experience developing and maintaining standard response documents, FAQs, and medical information repositories.
• Familiarity with the Medical, Legal, and Regulatory review process and standards for promotional and scientific materials.
• Ability to interpret clinical and real‑world data—including study endpoints, confidence intervals, and effect sizes—and communicate findings accurately to scientific and lay audiences.
• Ability to translate scientific evidence into clear, unbranded educational content for HCP audiences.
• Proven ability to partner effectively across Medical Affairs, Regulatory, Marketing, and Commercial teams to align messaging and ensure compliance.
• Commitment to high standards of accuracy, regulatory compliance, and ethical practice in all deliverables.
• Ability to manage multiple projects, prioritize effectively, and deliver under tight timelines.
• Strong influencing, facilitation, and presentation abilities; capable of serving as a medical information subject matter expert internally and externally.

Benefits

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.

EEO Statement

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.