Senior Medical information Writer

Employvision Inc.; United States; Remote; USD 56,000 - 105,000; Part time

Job summary

Employvision Inc. is seeking a skilled Medical Writer to support the global medical content development for medical affairs. This remote, part-time role demands strong expertise in creating scientific content across various therapeutic areas and involves collaboration with internal teams to ensure regulatory compliance.

Benefits

Flexible work hours

Collaborative team environment

Diverse client projects

Qualifications

• Minimum 2 years in medical information or communications roles.
• Experience in developing medical content (SRDs, FAQs, CRDs).
• Proficient in medical literature search tools.

Responsibilities

• Develop medical content including SRDs, FAQs, and training materials.
• Manage content development process from writing to review.
• Collaborate with teams on content strategy and improvements.

Skills

Analytical skills

Critical thinking

Project management

Communication

Education

MSc, PharmD, PhD in Life Sciences, Medicine, Pharmacy

Tools

Veeva PromoMats

PubMed

EndNote

Mendeley

Job description

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Title: Medical Information Writer -Senior

Location: Remote in USA

Duration: 3 -6+ months

Medical Writer – Medical Information & Content Development (Part-Time/Flexible)

We are seeking a skilled Medical Writer with experience in developing high-quality medical information deliverables such as Scientific Response Documents (SRDs), FAQs, and standard response documents. This role supports global medical content development for medical affairs and information functions.

• Hours: 20–30 hours/week with flexibility to increase to 40 hours/week as needed
• Travel: Up to 10–15%
• Location: Remote
• Start: Immediate or based on availability

Role Summary

The Medical Writer will contribute to the development and management of scientifically rigorous, regulatory-compliant medical content to support client needs. This includes collaborating with internal teams and clients to craft impactful, accurate materials across multiple therapeutic areas.

Key Responsibilities

• Develop a range of medical content including SRDs, FAQs, custom response documents, slide decks, abstracts, posters, training materials, etc.
• Lead the end-to-end content development process: gather background materials, write scientifically accurate content, and manage internal and client review cycles.
• Participate in medical, legal, and regulatory (MLR) reviews and discussions.
• Use document management systems (e.g., Veeva PromoMats, MedComms) for content submission, annotation, and tracking.
• Perform literature reviews and scientific fact-checking as needed.
• Collaborate with cross-functional teams and contribute to content strategy, execution, and process improvements.
• Support development and updates of SOPs, templates, and style guides.
• Participate in client meetings and provide strategic input when required.
• Stay updated on best practices and regulatory standards in medical writing and medical information.

Required Qualifications

• Education: MSc, PharmD, PhD, or equivalent in Life Sciences, Medicine, Pharmacy, or a related field.
• Experience:
• Minimum of 2 years in medical information, medical communications, or related industry roles.
• Proven track record in developing medical information content (SRDs, FAQs, CRDs, etc.).
• Proficiency in medical literature search tools (e.g., PubMed, Embase) and reference management software (e.g., EndNote, Mendeley).
• Strong understanding of regulatory and compliance requirements for promotional and non-promotional materials.
• Skills:
• Strong analytical and critical thinking skills.
• Competence in Microsoft Office and Adobe Acrobat.
• Ability to manage multiple projects and deadlines.
• Collaborative mindset with the ability to work independently.

Preferred Qualifications

• Advanced degree (PharmD, MD, PhD).
• Experience with global medical content development for product launches and life-cycle management.
• Background in various therapeutic areas.
• Familiarity with content review systems (e.g., Veeva PromoMats).
• Demonstrated ability to deliver high-quality results and drive client satisfaction.
• Strong ethical and professional integrity.

What We Offer

• Flexible work hours and remote setup
• Collaborative and supportive team environment
• Opportunity to work on diverse client projects across therapeutic areas

If you are a driven medical writer passionate about clear, compliant scientific communication and want to make an impact in the medical affairs space, we’d love to hear from you.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Writing/Editing, Art/Creative, and Science

• Industries

  Pharmaceutical Manufacturing

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