Remote Medical Writer – MedTech Regulatory & Clinical

Rqmplus; Polska; Hybrid; PLN 90,000 - 130,000; Full time

Job summary

RQM+ is seeking a Medical Writer to develop Clinical, Regulatory, and Regulatory-technical documents for global medical device clients. The role emphasizes literature reviews, regulatory reporting, and collaboration with cross-functional teams to ensure high-quality, compliant submissions.

Requirements include residence in Poland, 0–2 years of experience, and a strong background in life sciences with excellent writing and communication skills.

Qualifications

• Reside in Poland.
• 0-2 years of experience in medical writing or related fields.
• Bachelor’s, Master’s or Ph.D. in life sciences or equivalent.
• Experience in medical writing within healthcare or academia.
• Strong medical and technical writing skills.
• Familiarity with Endnote and PubMed.
• Strong scientific writing with attention to detail.
• Ability to work independently and take initiative.
• Excellent organizational skills for multiple projects and tight deadlines.
• Willingness to align with RQM+ values and culture.

Responsibilities

• Develop and write Clinical, Regulatory, and Technical documents.
• Prepare and edit Clinical Regulatory Reports (Clinical Evaluations, Post Market Surveillance, CRRs).
• Perform literature searches for Safety and Performance data.
• Collaborate with cross-functional teams to analyze clinical data.
• Stay current with global regulations and guidance affecting regulatory writing.
• Ensure documents comply with RQM+ procedures and guidelines.
• Interact with clients to gather information and provide updates.

Skills

Medical writing

Regulatory knowledge

Attention to detail

Communication skills

Independent working

Education

Bachelor’s/Master’s/PhD in life sciences

Tools

Endnote

PubMed

Job description

RQM+ is seeking a Medical Writer to develop Clinical, Regulatory, and Regulatory-technical documents for global medical device clients. The role emphasizes literature reviews, regulatory reporting, and collaboration with cross-functional teams to ensure high-quality, compliant submissions.

Requirements include residence in Poland, 0–2 years of experience, and a strong background in life sciences with excellent writing and communication skills.