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Document Review Specialist II/Senior Document Review Specialist (FSP)

Thermo Fisher Scientific -
Maryland

Apply Now

Job Details

Full-time
$85,000 - $100,000 a year
3 days ago

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

English
Clinical research protocol review

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Summarized Purpose:

We are excited to be expanding our Medical Writing Functional Service Partnership (FSP) Team in North America. We are seeking an experienced and skilled Document Review Specialist II who will be dedicated to one or more clients in the FSP space to join our team; experience working in a range of document management systems would be preferred. As a remote-based Document Review Specialist within the FSP Team, you will effectively review regulatory documents, including but not limited to submissions documents, protocols and amendments, clinical study reports, investigator’s brochures, and patient safety narratives, to ensure quality standards and adherence to templates, client guidelines, editorial style guides, and industry standards. You will collaborate with internal clients, supporting and enabling effective communication that results in operational excellence and quality deliverables. This role requires meticulous attention to detail, a high English proficiency with the ability to communicate clearly and concisely, and a solid understanding of regulatory document content.

Key Responsibilities:

Reviews highly technical scientific documents of all types developed within or outside of the company to ensure quality standards that meet or exceed client expectations.
Verifies scientific logic and clarity of the document by verifying data in tables, listings, and figures against source documents, checking for consistency according to current regulatory standards and guidelines.
Edits for accuracy, consistency, and grammatical correctness.
Adjusts schedule to accommodate unexpected requests for priority review.
Revises scientific language for usage, flow, clarity, and audience appropriateness.
Proactively queries authors to ensure compatibility with unique preferences and scientifically sound judgment.
Maintains, communicates, and applies knowledge of current guidelines, templates, and industry standards.

**This is a document review role only and you will not be responsible for writing**

Education and Experience:

Bachelor's degree or equivalent and relevant formal academic/vocational qualification required.
5 years of regulatory document review experience, including protocols, protocol amendments, clinical study reports, narratives, investigator brochures, regulatory responses, and submission modules (primarily Modules 2.5, 2.7.3, and 2.7.4).
Experience working in the pharmaceutical/CRO industry preferred.
If CRO experience: experience working in a client-dedicated role or with 1 to 2 clients over multiple projects is preferred.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Capable of focusing on document details and the overall objectives and intent of document messaging.
Good knowledge of the methods, techniques, and procedures of medical writing tasks.
Strong analytical ability.
Good working knowledge of medical terminology, statistical concepts, GCP, guidelines (e.g., ICH), and requirements of the FDA and other international regulatory agencies.
Attentive to detail and quality of documents, thorough and methodical.
Proficient oral and written communication and grammatical skills.
Good organizational and planning skills.
Good interpersonal skills.
Proven ability to work effectively in a team environment.
Advanced computer literacy and expertise.
Good knowledge and understanding of document management systems.
Capable of working well under pressure and remaining motivated.
Capable of working both independently and collaboratively with a team in a cross‑cultural, geographically dispersed environment.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

The salary pay range estimated for this position Medical Doc Review Specialist II based in Maryland is $85,000.00–$100,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

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Document Review Specialist II/Senior Document Review Specialist (FSP)

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