Discover Impactful Work:

We are looking for a Senior Document Review Specialist to join our FSP Medical Writing team. This role would be dedicated to one client and fully remote, working from certain EMEA locations. As a Senior Document Review Specialist, you will review documents to ensure quality of a standard that meets or exceeds client's expectations. Documents include: regulatory submissions, integrated clinical study reports, serious adverse event narratives, study protocols and publications. You will be ensuring integrity of data in tables against source documents, instructing others outside of the quality review group on the review process.

A Day in the Life:

• Reviews highly technical documents of all types to ensure a quality standard that meets or exceeds client expectations.

• Ensures scientific logic and clarity of the document by verifying data in tables 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.

• Coordinates the work of team members and tracks the status of documents being reviewed.

• Mentors junior team members.

• May represent the department at meetings with clients.

• Contributes to the development and modification of the quality review process.

• Collaborates with the writer to manager alliance account(s)

• Delegates weekly assignments to the quality review team and fields questions as appropriate."

Keys to Success:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years').

Capable of concentrating on the details of a document without losing sight of the overall objectives and intent of the document's message

Thorough knowledge of medical terminology, statistical concepts, GCP, guidelines (e.g. ICH), and requirements of the FDA and other international regulatory agencies

Familiarity with interpreting data and excellent analytical ability

Effective oral and written communication skills

Good organizational and planning skills

Good interpersonal skills

Ability to work on own initiative

Good computer literacy and expertise

Competent word processing skills

Solid understanding of document management systems

Suitable level of expertise within a broad range of medical writing projects

Good knowledge of global and regional medical writing and regulatory affairs duties for clinical trials, marketing authorization and late-phase procedures

Capable of providing general advice and training to others

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"

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.