Senior Medical Writer

Aixial Group; United Kingdom; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

Aixial Group, a leading Contract Research Organization, seeks a Senior Medical Writer to coordinate medical writing tasks in clinical trials. The successful candidate will deliver high-quality documents in compliance with regulations, ensuring alignment with company values. This role offers opportunities for professional growth in a supportive work environment.

Benefits

Professional growth opportunities

Friendly work environment

Qualifications

• Experience in writing clinical study reports and protocols.
• Familiarity with ICH-GCP guidelines.
• Strong attention to detail and ability to manage multiple tasks.

Responsibilities

• Coordinate and manage medical writing tasks.
• Deliver high-quality documents for regulatory submission.
• Provide timely feedback on work progress.

Skills

Medical Writing

Regulatory Compliance

Communication

Education

Degree in Life Sciences or Relevant Field

Job description

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The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, with offices located in France, UK, US, Belgium, Denmark, Sweden, Switzerland, Romania, and India.

The CRO occupies a unique position in the clinical research industry, supporting biotech in clinical trials across all phases (Ph. I – IV) and non-interventional studies, as an expert in the operational delivery of clinical trials. Our vision is to conduct clinical trials better than anyone else, to help patients and ultimately save lives. We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials.

We are currently looking for an enthusiastic and talented Senior Medical Writer for a client dedicated opportunity. This role is home-based in the UK or EU, or office-based/hybrid in Denmark and Sweden.

The successful candidate will be responsible for coordinating and managing medical writing tasks, including the timely delivery of high-quality documents in accordance with agreements made between Aixial and the sponsor. Key medical writing tasks include clinical study reports, Investigator’s Brochure (IB) updates, protocols, as well as summary documents and clinical overviews for submission to regulatory authorities. The candidate will be expected to work in alignment with company values and in compliance with ICH-GCP, national and international regulations, and the client’s quality system. They must provide timely feedback to management on work progress and actively participate in scheduled training sessions and required reading. Other medical writing tasks may be assigned as needed. Aixial offers a friendly and stimulating work environment, with ample opportunities for professional growth.