Senior Medical Writer

JR United Kingdom; North East; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

A leading Medical Communications Agency is looking for experienced Senior Medical Writers to join their team in Newcastle-upon-Tyne. This role offers a chance to produce high-quality scientific content while mentoring junior writers. The company promotes work-life balance with a 35-hour work week and flexible work arrangements.

Benefits

35-hour workweek

Flexible remote/hybrid working options

Career progression to Lead Medical Writer

Qualifications

• Proven experience as a Senior Medical Writer within pharma, biotech, or CRO settings.
• Demonstrated expertise in at least one therapeutic area: Oncology, Cardiovascular, Respiratory, or Ophthalmology.
• Excellent scientific writing and editing skills.

Responsibilities

• Develop, write, and edit scientific documents such as clinical study reports.
• Ensure documents meet accuracy, clarity, and regulatory standards.
• Mentor junior writers and support team knowledge sharing.

Skills

Scientific writing

Project management

Communication

Teamwork

Job description

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Senior Medical Writer, newcastle-upon-tyne, tyne and wear

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Client:

Meet Life Sciences

Location:

newcastle-upon-tyne, tyne and wear, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

5

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

We are partnering with a recognised Medical Communications Agency, consistently ranked among the Top 10 Best Places to Work. They are currently recruiting experienced Senior Medical Writers for multiple openings. These roles are suited to professionals with strong medical writing backgrounds who are ready to advance their careers. Successful candidates will produce high-quality scientific content across various therapeutic areas, with opportunities to progress into Lead Medical Writer roles.

Key Responsibilities:

• Develop, write, and edit scientific documents such as clinical study reports, manuscripts, regulatory submissions, and medical communications.
• Ensure documents meet accuracy, clarity, and regulatory compliance standards.
• Collaborate effectively with clinical, regulatory, and medical affairs teams.
• Mentor junior writers and support team knowledge sharing.
• Contribute to the team’s growth with a view to future leadership responsibilities.

Therapeutic Specialisations Required (experience in at least one):

• Oncology
• Cardiovascular, Respiratory, Oncology & Ophthalmology

Candidate Profile:

• Proven experience as a Senior Medical Writer within pharma, biotech, or CRO settings.
• Demonstrated expertise in at least one of the specified therapeutic areas.
• Excellent scientific writing and editing skills.
• Strong project management abilities and ability to meet deadlines.
• Effective communication and teamwork skills.
• Flexible to work remotely or onsite (2 days per week depending on location).

Why This Opportunity?

• Join a top-ranked company recognized for its exceptional work culture.
• Benefit from a 35-hour workweek supporting work-life balance.
• Flexible remote or hybrid working options.
• Clear pathways for career progression into Lead Medical Writer roles.
• Work across multiple therapeutic areas and exciting projects.