- Regulatory Affairs
Description
Job Title: Medical Writer
Working Schedule: Full-time, Permanent
Location: EU Remote
About Stirling Q&R:
Stirling Q&R, under the leadership of Chris Stirling, stands out as a premier executive search firm, typically specializing in Quality & Regulatory roles within the life sciences industry. Our expertise spans permanent and contract recruitment for mid to senior-level positions in Pharma, Biotech, and Medical Device sectors.
About the Client:
Our client, a prominent regulatory consultancy headquartered in the Netherlands, extends the opportunity for remote work in the BeNeLux region. Their commitment to innovation, excellence, and a collaborative work environment makes them a sought-after employer.
Medical Writer Job Requirements:
- Proven experience as a Medical Writer or in a related writing position.
- Strong ability to work independently, demonstrating a high level of self-motivation.
- Eagerness to learn, develop, and excel in a challenging and innovative environment.
- Proficiency in regulatory writing, encompassing document preparation for regulatory submissions.
- Knowledgeable about industry guidelines and regulations (e.g., ICH, FDA, EMA).
- A comprehensive understanding of clinical research and the drug development process.
Education and Experiences for the Medical Writer Role:
- MSc/PhD in Pharmacy, Biomedical Sciences, or Life Sciences.
- Minimum of 3 years of experience in Medical Writing.
- Exceptional scientific and technical writing and editing skills in English.
Apply Today for the Medical Writer Position!
If you are a motivated and skilled Medical Writer ready to shape the future of healthcare communication, apply now. Your expertise as a Medical Writer will be instrumental in their commitment to innovation and excellence. Join them in this exciting journey, and let your impact be profound!
$ads={1}