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Document Writer Jobs in Raleigh, NC (NOW HIRING)

Acts as Lead Medical Writer on any type of writing project and can advise others on any type of ... Take a leading role in preparing assigned documents, including, but not limited to, confirming the ...

Acts as Lead Medical Writer on any type of writing project and can advise others on any type of ... Take a leading role in preparing assigned documents, including, but not limited to, confirming the ...

NC FAST P4 Test Scripts Writer Location : Research Triangle Park, Durham, NC REQ ID: 496061 ... Documents, developing requirements into test conditions, cases and scripts, development and ...

Senior Technical Writer

Raleigh, NC · On-site

$50 - $60.25/hr

Description The Technical Writer III is an experienced technical documentation professional who works independently with minimal supervision. This person owns significant project workstreams ...

Test Scripts Writer Location: Durham, NC 27709 Duration: 12+ months contract Rate:$30/hr on C2C ... Documents, developing requirements into test conditions, cases and scripts, development and ...

Test Scripts Writer Duration 12 Months Location: Durham, NC Description: Duties include analyzing ... Documents, developing requirements into test conditions, cases and scripts, development and ...

Senior Technical Writer

Raleigh, NC · On-site

$50 - $60.25/hr

Description The Technical Writer III is an experienced technical documentation professional who works independently with minimal supervision. This person owns significant project workstreams ...

Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and ... Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps ...

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and ... Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps ...

Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and ... Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps ...

They are seeking a Technical Writer in Raleigh, NC to create and manage technical documentation for an IT audience. Responsibilities : • Demonstrated experience writing technical documentation for ...

... technical documentation and training materials using various Microsoft Office tools ... Responsibilities : • The technical writer will be expected to heavily use the Microsoft Office ...

We offer an excellent compensation package We are looking for Sr. Technical Writer in Raleigh, NC ... Documented experience in developing IT Operational processes and Procedure * Experience meeting ...

Our writers are integral members of clinical development teams supporting the writing and ... Ensuringthat all documents are produced according to agreed timelines,monitorand manage project ...

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Document Writer information

See Raleigh, NC salary details

$20

$34

$52

How much do document writer jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for document writer in Raleigh, NC is $34.98, according to ZipRecruiter salary data. Most workers in this role earn between $23.37 and $48.61 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Document Writer, and why are they important?

To thrive as a Document Writer, you need excellent written communication skills, attention to detail, and proficiency in language usage, typically supported by a relevant degree or experience in writing or communications. Familiarity with word processing software, document management systems, and sometimes industry-specific tools like Adobe Acrobat or content management systems is common. Strong research abilities, time management, and adaptability help Document Writers effectively convey complex information and meet deadlines. These skills ensure documents are accurate, clear, and tailored to their intended audience, which is essential for effective communication and organizational success.

What are some common challenges faced by Document Writers when working with subject matter experts (SMEs)?

Document Writers often collaborate closely with subject matter experts to gather accurate information, but a common challenge is translating complex or technical details into clear, accessible documentation for the intended audience. SMEs may use specialized jargon or provide dense information, so Document Writers need strong communication skills to clarify requirements and ensure nothing is lost in translation. Building rapport and maintaining regular communication with SMEs can help streamline the process and lead to more effective, user-friendly documents.

What does a Document Writer do?

A Document Writer is responsible for creating, editing, and formatting various types of documents such as reports, manuals, proposals, and business correspondence. They ensure that documents are clear, well-organized, and tailored to the intended audience. Document Writers often work closely with subject matter experts to gather information and may use specialized software to maintain consistency and quality. Their role is essential in ensuring effective communication within an organization.
Medical Writing Manager/Senior Manager - USA

Medical Writing Manager/Senior Manager - USA

Trilogy

Durham, NC • On-site, Remote

$160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

Trilogy Writing & Consulting, anIndegenecompany,is currently looking to hireaMedical WritingManager/Senior Manager, reporting directly to the Director of Medical Writing,to support our growing company in producing regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our writers are integral members of clinical development teams supporting the writing andcoordinationof successful documentation across a broad spectrum of therapeutic areas. As our company continues to expand, there is room to develop withusand your ideas will form our future together. For further insight into who we are and what we do, please explore our website (www.trilogywriting.com).

Applicants must live in the USA and be authorized to work for any employer in the USA (we are unable to sponsor or take over sponsorship of an employment visa at this time); may work either fully remotely or a hybrid schedule (in office/remote) from our Durham, NC, USA office.

Job Overview:

As aMedical Writing Manager/Senior Manager, you will:

  • Provide line managementofa group ofmedicalwriters.
  • Provideresource oversightand guidance on a weekly basis.
  • Overseeprofessional development includingregular (i.e.quarterly) meetings with all members of the honeycomb.
  • Conduct annual and ad-hoc performance reviews for all members of the honeycomb.
  • Overseeeach employee's timeandutilization.
  • Regularly reinforce the company's values and purpose tomaintaina sense of shared values, purpose, mission, and vision
  • Participate in Trilogy management-levelactivities.
  • Participate inbusiness development activities such as giving talks or workshops on behalf of Trilogy,participatingin management meetings to discuss strategic developments for the company,orrepresentingTrilogy at meetings withclients.
  • In addition,continue writing on client projects but have a reduced writing workload to accommodate these management activities.

Required experience and qualifications (professional skills) for this role:

  • Experience managing a team of medical writers inaline-management functionfor a minimum of 2 years.
  • A minimum of8years of medical regulatory writing experiencein a pharmaceutical, biotech, or CRO environment.
  • Demonstrated abilityand experience as a Lead Medical Writer on multiple types of regulatory documents/writing projects, including complex, multiple-document projectswith global, multinational teamssuch as submission dossiers or responses to regulatory authorities.
  • Experience in managementand coordination ofproject-level activities, including oversight of resources, otherwritersand QC, as well asuse ofsystematic methods to plan and perform tasks and coordinate people.
  • Experience with cost/benefit analyses for decision making (e.g.regardingresource assignment, conflict resolution, etc.)
  • Excellent interpersonal skills includingabilitytoguide andinfluence others internally and/or externally, effective decision-makingability,and excellent written and oral communication skills.


Trilogy offers the following:

  • Competitive base salary (starting from$160,000USD;dependent onexperience level and the Company's compensation practices)
  • Annual bonusopportunity dependent on personal and company performance
  • A generous allowance of paid time off (vacation, holiday, illness).
  • Comprehensive benefit plansthatinclude medical, dental, vision, short- and long-term disability, life insurance with AD&D.
  • Retirement savings plan with company match
  • Full AMWA membership and annual conference attendance paid for by Trilogy
  • Continuous personal and professional development opportunities
  • Free weekly yoga sessions
  • Other fun and excitingevents toencourage team bonding and development


Indegene is an Equal Opportunity Employer committed to fostering a culture of inclusion, diversity, and respect. We do not discriminate against any individual on the basis of race,color, religion or belief, sex, sexual orientation, gender identity or expression, age, national or ethnic origin, disability, marital or parental status, or any other characteristic protected under applicable laws. All employment decisions, including recruitment, hiring, training, compensation, promotion, and separation, are made based on business needs, individual merit, and qualifications.


It is important toIndegeneto ensure the highest possible degree of protection for your personal data. All personal data collected and processed within the scope of an application for employment with Trilogy are protected against unauthorized access and manipulation by technical and organizational measures and are notforwardedto third parties.Your data will be collected for the purpose of filling employment opportunities offered by Trilogy Writing & Consulting GmbH in Germany or its subsidiaries Trilogy Writing & Consulting Ltd in the UK,Trilogy Writing & Consulting, LLC in Canada,and Trilogy Writing & Consulting, Inc. in the USA.Bysubmittingyour data with this application, you consent to its use for this purpose within Trilogy. You can revoke this consent at any time without needing to give a reason by informing us of your revocation under jobs@trilogywriting.com.In the event ofrevocation, we willdeleteyour personal dataimmediately.