🕒 Yesterday
Medical Writer I preparing and quality-controlling clinical and regulatory documents for ICON, a global clinical research organization. Managing EDMS workflows, CSR lifecycle support, and regulatory submission readiness.
🕒 4 days ago
Medical writer leading clinical, regulatory, and scientific documents for Syneos Health, a life sciences services organization. Collaborating with biopharmaceutical clients and cross-functional clinical teams.
🕒 6 days ago
Medical Writer developing clinical and regulatory documents for Thermo Fisher Scientific’s global clinical research services. Ensuring compliant, accurate deliverables across pharmaceutical and CRO projects.
🕒 6 days ago
Principal Medical Writer producing clinical and regulatory documents for Syneos Health’s drug-development services. Coordinating reviews, clients, cross-functional teams, and complex medical writing projects.
🕒 August 5
Senior Medical Writer developing clinical and regulatory documents for Parexel, a global clinical research organization. Coordinating reviews, quality control, approvals, and publishing across clinical development teams.
🌐 Poland, Romania, +2 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🏥📝 Medical Writer
🕒 August 5
Medical Writer II preparing clinical and regulatory documents for Parexel, a global clinical research organization. Coordinating reviews, quality control, timelines, approvals, and publishing across clinical development programs.
🌐 Poland, Spain, +2 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🏥📝 Medical Writer
🕒 August 5
Medical Writer developing clinical and regulatory documents for Parexel, a global clinical research organization. Managing document workflows, reviews, quality control, approvals, and publishing across clinical development programs.
🌐 Poland, Spain, +2 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer
🕒 August 4
Senior/Principal Medical Writer producing clinical regulatory documents for the international pharmaceutical industry. Leading client collaboration, document reviews, timelines, budgets, and writer coordination.
🕒 August 4
Senior/Principal Medical Writer producing clinical regulatory documentation for the international pharmaceutical industry. Leading writing, client coordination, review cycles, timelines, budgets, and regulatory document management.
🕒 August 4
Principal Medical Writer preparing clinical regulatory documentation for international pharmaceutical companies. Leading authoring, client coordination, review cycles, budgets, and timelines across therapeutic areas.
🕒 August 4
Principal Medical Writer producing clinical regulatory documents for the international pharmaceutical industry. Leading multinational projects, timelines, reviews, budgets, and writer coordination.
🕒 August 4
Medical Writer creating scientific communications for Lumanity’s life-sciences clients. Developing manuscripts, training materials, and client-facing content across therapeutic areas.
🕒 July 31
Medical Writer preparing clinical documents for Parexel, supporting clinical trials and regulatory submissions in a collaborative environment.
🕒 July 30
Senior Medical Writer delivering medical writing services for clinical documents at Parexel. Collaborating closely with sponsors to ensure high-quality clinical development programs in healthcare.
🕒 July 29
Senior Medical Writer at BOLDSCIENCE developing a range of medical communication materials. Involves technical writing, client communications, and project management responsibilities.
🕒 July 29
Lead Medical Writer at BOLDSCIENCE developing and delivering medical communications across various projects. Ensuring quality, mentoring junior writers, and collaborating with teams on client needs.
🕒 July 29
Medical Writer at Syneos Health leading clinical documentation efforts in drug development. Collaborating with cross-functional teams to produce high-quality medical writing deliverables.
🕒 July 28
Medical Writer in Global Cardiac Solutions team creating expert reports and documentation. Collaborating with scientists and stakeholders to ensure regulatory compliance and high-quality outputs.
🇬🇧 United Kingdom – Remote
💰 Private Equity Round on 2019-10
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer
🕒 July 27
Senior Medical Writer/Principal Medical Writer leading the development of high-quality clinical study documents. Writing, editing, and collaborating on documents in compliance with regulatory guidelines.
🇬🇧 United Kingdom – Remote
💵 $100.6k - $182.6k / year
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟠 Senior
🏥📝 Medical Writer
🕒 July 27
Senior Medical Writer leading high-quality clinical study document development for Precision Medicine Group. Responsible for document planning, writing, and compliance with regulatory guidelines.
🇬🇧 United Kingdom – Remote
💵 $100.6k - $182.6k / year
💰 $35.2M Venture Round on 2021-03
⏰ Full Time
🟠 Senior
🏥📝 Medical Writer
+19 More Medical Writer Jobs Available!
The average salary for remote medical writers in Europe is €81,225 per year. This is based on data from 157 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
🟢 Junior Medical Writer (1-2 yrs) | 19 | €46,000 |
🟡 Mid-level Medical Writer (2-4 yrs) | 26 | €46,000 |
🟠 Senior Medical Writer (5-9 yrs) | 82 | €130,272 |
🔴 Lead Medical Writer (10+ yrs) | 30 | €0 |
We analyzed 110 job listings in the last year and found it takes about 40 days for employers to close a job opening.
We reviewed 157 job postings and found the top 10 skills employers are asking for most often are:
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs as soon as they're posted, so you can apply before everyone else.
Most members hear back within the first week
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