Sr. Medical Writer

TALENT Software Services; California (MO); Remote; USD 96,432 - 110,208; Full time

Job summary

A consulting firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review timelines within a collaborative team environment. Candidates should have a scientific degree and significant experience in medical writing, with advanced knowledge of drug development processes and regulatory requirements. This full-time position is primarily remote, with a competitive pay range of $70 - $80 per hour.

Qualifications

• Minimum 6 years as a medical writer in pharmaceutical industry or 10 years in a related field.
• Experience with INDs and regulatory submissions preferred.
• Ability to interpret complex clinical data and present it clearly.

Responsibilities

• Draft and edit clinical study protocols and reports.
• Manage timelines and facilitate document review processes.
• Represent Global Medical Writing in cross-functional team meetings.

Skills

Medical writing experience

Regulatory document knowledge

Attention to detail

Effective communication

Education

Bachelor's or higher degree in scientific field

Tools

Microsoft Word

Adobe Acrobat

Document management software

Job description

Pay Range

This range is provided by TALENT Software Services. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$70.00/hr - $80.00/hr

Sr. Medical Writer

Job Summary: Talent Software Services is in search of a Sr. Medical Writer for a contract position in CA (Remote). The opportunity will be six months with a strong chance for a long-term extension.

Position Summary: This position progressively develops the medical writing function in alignment with the requirements of the Development Sciences department and organizational goals. Filling this need with a regular full-time employee will enable Client to reduce writing-related CRO and contractor costs, increase Global Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications.

Primary Responsibilities/Accountabilities

• Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
• Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PBRERs, DSURs, etc.)
• Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
• Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
• Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
• Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
• Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
• Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
• Adheres to departmental procedures and practices and technical and industry standards during all aspects of work
• Works effectively with cross-functional groups within Client's
• Other tasks as assigned

Qualifications

• Bachelor's or higher degree required; scientific focus desirable
• Minimum requirement: Experience in medical writing
• Evidence of medical writing career development desirable, e.g., American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association

Fulfills one of the following:

• Up to 6 years as a medical writer in the pharmaceutical industry
• At least 10 years of medical or scientific writing experience as a primary job responsibility
• Clinical Studies
• Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
• Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Intermediate to advanced applied knowledge of

• Documentation required for the conduct of clinical studies
• Protocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs)
• Study results reporting
• Integrated results reporting
• Direct experience with documentation in all phases of drug development

Medical Writing

• Experience writing, reviewing, or editing protocols and clinical study reports required
• Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
• Experience writing, reviewing, or editing regulatory briefing books preferred
• Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
• Ability to interpret and create complex tabular and graphical clinical data presentations
• Advanced applied knowledge of basic clinical laboratory tests
• Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)

Computer/office equipment Skills

• Proficient in Microsoft Word (including the use of templates), Excel, Adobe Acrobat, MS Project/Project Server, and PowerPoint
• Experience using document management software (eg, LiveLink, SharePoint, Veeva)
• Experienced with scanners, printers, and copiers

Regulatory

• Intermediate to advanced knowledge of regulatory requirements and guidances associated with standalone regulatory documents (eg, protocols, investigator brochures, and clinical study reports)
• Prior familiarity with standard eCTD IND/NDA work, including:
  • Modules 2, 3, 4, and 5 of INDs/NDAs in eCTD format
  • Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISS)

Project Management

• Capable of working on multiple tasks and shifting priorities
• Capable of leading a cross-functional team under strict timelines, including calling/running meetings and managing team review and comment adjudication stages of document preparation
• Capable of representing Global Medical Writing at cross-functional meetings, advocating for Global Medical Writing, and working with Global Medical Writing line management to resolve cross-functional conflicts
• Good conflict management skills
• Motivated and shows initiative
• Detail oriented

Communication

• Capable of well organized, concise and clear written and verbal communication
• Capable of comprehending complex scientific concepts and translating them into clear, concise, appropriately referenced text that meets regulatory requirements
• Effective at explaining writing principles to a varied audience both in individual and group settings; intermediate to advanced presentation skills

If this job is a match for your background, we would be honoured to receive your application! Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let's talk!

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Other
• Industries: IT Services and IT Consulting

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