Medical Writer (Regulatory) — Hybrid & Flexible Hours

Ctc Clinical Trial Consultants AB; Uppsala län; Hybrid; SEK 520,000 - 700,000; Full time

Benefits offered by this job

Flexible working hours

Wellness allowance

Generous vacation terms

Hybrid work in Uppsala

Job summary

CTC Clinical Trial Consultants AB in Sweden is seeking an experienced Medical Writer to join a team of MWs responsible for writing and quality‑checking regulatory documents, clinical study protocols and reports.

The role is hybrid in Uppsala, full‑time, with opportunities for professional development and to mentor colleagues. Requirements include MSc in life sciences, 3+ years in medical writing, and English proficiency; Swedish knowledge is also valued.

Qualifications

• At least 3 years of experience in medical writing, drug development, and clinical trials.
• Excellent written English and ability to express complex data clearly.
• Experience leading meetings and coordinating multiple timelines.

Responsibilities

• Write protocols and reports per ICH E6/E3 and ISO 14155, coordinating QC and client reviews.
• Draft regulatory texts like summaries, narratives, amendments, and authority responses.
• Coordinate and lead meetings; act as client contact, and mentor colleagues.
• Other tasks such as medical coding, abstracts, safety reports, and marketing texts.

Skills

Medical writing

Clinical trials

Regulatory writing

Project coordination

English proficiency

Swedish language

Education

MSc in life sciences

PhD in life sciences (preferred)

Job description

CTC Clinical Trial Consultants AB in Sweden is seeking an experienced Medical Writer to join a team of MWs responsible for writing and quality‑checking regulatory documents, clinical study protocols and reports.

The role is hybrid in Uppsala, full‑time, with opportunities for professional development and to mentor colleagues. Requirements include MSc in life sciences, 3+ years in medical writing, and English proficiency; Swedish knowledge is also valued.