Senior Medical Information Writer

EVERSANA; London; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading medical consulting firm is seeking a Senior Medical Information Writer based in London. The ideal candidate will have a Doctorate or MSc in Life Sciences and at least two years' experience in medical writing. Responsibilities include developing scientifically accurate content for clients and collaborating with various teams. This remote position allows for flexibility while maintaining high-quality standards. Competitive salary and benefits are offered, including generous paid time off and retirement resources.

Benefits

Generous paid time off

Employer-funded tuition reimbursement

Health, dental, and vision insurance

Global workplace flexibility

Qualifications

• Minimum of 2 years of experience in medical information.
• Experience developing medical information materials.
• Strong understanding of regulatory requirements.

Responsibilities

• Develop and manage medical content for clients.
• Collaborate with teams to ensure quality and compliance.
• Conduct literature searches and fact-checking.

Skills

Exceptional written and oral skills

Ability to interpret complex scientific information

Proficient in Microsoft Office

Project management skills

Experience in medical writing

Education

Doctorate or Master of Science degree in Life Sciences

Tools

Microsoft Office

PubMed

EndNote

Job description

Social network you want to login/join with:

Senior Medical Information Writer, London

col-narrow-left

Client:

EVERSANA

Location:

London, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

8ce65c037d0f

Job Views:

3

Posted:

01.08.2025

Expiry Date:

15.09.2025

col-wide

Job Description:

Job Description

We are looking for a Senior Medical Information Writer with a minimum of 2 years of recent experience in developing core medical information deliverables, including Standard Response Documents (SRDs), Frequently Asked Questions (FAQs), Custom Response Documents, and interactive SRDs. This is a remote position, offering flexibility while working on impactful projects. The ideal candidate should be capable of independently managing assignments and consistently delivering high-quality, scientifically accurate content with minimal supervision.

This role can be based in the UK, Ireland, Spain, Italy, Poland, Germany or Portugal.

Must be legally eligible to work in the European Union / United Kingdom.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by:

• Plays an essential role supporting Global Medical Information / Medical Content Development Team on content development-related engagements for clients who require medical content development and management services.
• Writes and creates medical and scientific content related to Medical Affairs, Medical Information and Medical Communications including, but not limited to, Scientific Response Documents (SRD), Frequently Asked Question (FAQ) documents, Slide Sets, Abstracts, Posters, Education and Training materials, and others for potential clients.
• Drives the client document development process from gathering materials and developing scientifically rigorous content to facilitating document review and discussions at medical, legal, regulatory (MLR) review meetings.
• Works with EVERSANA and/or client-provided document management technology platforms (i.e., Veeva PromoMats / MedComms, etc.) as content owner when appropriate, uploading documents, providing reference anchoring and annotations as required.
• May be called up to perform scientific data fact checking for documents in support of medical reviewers participating in MLR teams.
• Collaborates with Global Medical Information / Medical Content Development Team and contributes to discussions on strategy, tactical execution and communication approaches for assigned projects.
• Provides direction and works closely with other medical writers and medical content development team to deliver on client projects efficiently and effectively.
• Participates in key client meetings as assigned.
• Supports creating/updating the SOPs, checklists, templates, style guides, and guidance documents as necessary.
• Stays knowledgeable of industry best practices and supports leadership team in evaluating and implementing new technologies and procedures to improve operational efficiency and quality of materials developed.
• Works collaboratively with other medical writers and creative teams across EVERSANA.
• All other duties as assigned

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

EXPECTATIONS OF THE JOB:

• Responsible to work collaboratively with EVERSANA medical information and medical affairs team and take direction and feedback from management and clients
• Responsible to ensure management and compliance with industry standards and codes of practice
• Able to work independently to develop high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content
• Responsible to proactively flag and manage any quality issues, and ensure timely corrective and preventive actions
• Travel This position may require business travel and will need to be able to travel up to approximately 10-15%.
• Hours: Able to work full time and be flexible with work scheduling as required by clients and management.

The above list reflects the general details necessary to describe the expectations of the position and shall not be construed as the only expectations that may be assigned for the position.

An individual in this position must be able to successfully perform the expectations listed above.

EVERSANA is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, national origin, age, veteran status, disability, or any other protected class. Applicants must be able to pass a drug test and background investigation.

Qualifications

MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:

The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.

• Education: Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare or equivalent.
• Experience and/or Training:
• A minimum of 2-year(s) experience in pharmaceutical industry or Medical Information / Medical Communications service provider. Experience developing global medical information materials, e.g., scientific response documents (SRDs), frequently asked questions (FAQs), custom response documents (CRDs), etc.
• Exceptional written, oral, interpersonal, and presentation skills including the ability to independently interpret and summarize complex results. Ability to establish credibility with a variety of audiences; especially with clients
• Ability to effectively interface with all levels of management and staff and to succeed in a matrix team setting while meeting or exceeding timelines.
• Proficient editing skills along with expertise in Microsoft Office, Acrobat and other applications.
• Experience conducting literature searches and working with tools such as PubMed, Ovid, Embase, etc.
• Experience working with reference management and citation software (e.g., EndNote, Mendeley, Citavi, etc.)
• Strong understanding of regulatory requirements and best practices in relationship to Medical Information, Medical Affairs and promotional and non-promotional materials review
• Excellent project management skills and proven track record of being results driven
• Ability to conceptualize, design and deliver best in class solutions.

PREFERRED QUALIFICATIONS:

• Education: A Pharm.D. or Pharm.M or a Degree in Medicine or PhD is preferred. Relevant Bachelor’s Degree in a Life Science also considered.
• Experience: Medical Information, Medical Communications, Medical Writing, Medical Affairs; experience developing medical content, especially Medical Information materials, for both new product launches and for updating and managing current materials; experience working across multiple therapeutic areas.
• Communication Skills: Possesses the ability to develop and articulate ideas and information that generate understanding and creates a climate that motivates and encourages others to participate.
• Analytical Thinking / Critical Thinking: Ability to analyze, digest, and interpret complex scientific information and data
• Project Management: Ability to develop project plans and execute on the project plan, both works individually and working with client(s), other medical content development team members, and medical information contact center team and leadership team.
• Results Driven: Proven track record of executing and delivering results.
• Innovator: Transforms creative ideas into original solutions that positively impact client delight and company’s performance.
• Highly Principled: Proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior.
• Client Management: Ability to manage, coordinate, and oversee relationship and projects with assigned client(s).
• Competitive Wages

  Above market salary structures as part of our total rewards program

• Retirement Resources

  Generous employer matching retirement solutions

Leading health, dental and vision insurance products

Employer-funded tuition reimbursement

• Global Workplace Flexibility

  Remote and hybrid work across the globe

• Paid Time Off

  Generous paid time off including company holidays

• Training & Development

  Company provided training and development

• Employee Assistant Programs

  Offering financial, work-life balance, legal solutions and more to employees at no cost 24-7-365