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Senior Medical Writer
2 months ago
We are seeking a highly skilled Senior Medical Writer to join our team at MAC Clinical Research. As a Senior Medical Writer, you will play a critical role in the development of clinical regulatory documents, including protocols, patient information sheets, informed consent forms, and clinical study reports.
Key Responsibilities:
- Author, review, and edit clinical regulatory documents to ensure accuracy and quality
- Collaborate with cross-functional teams to gather and incorporate relevant information
- Provide mentoring and guidance to junior writers and support the development of the Medical Writing team
- Manage document review cycles and ensure timely delivery of high-quality documents
- Participate in data-focussed discussions and contribute to the development of project plans and documentation
Requirements:
- Master's or PhD in life sciences, medicine, pharmacy, or a related discipline
- Proven experience in medical writing, preferably in a clinical research environment
- Strong knowledge of regulatory requirements and clinical trial processes
- Excellent written and verbal communication skills
- Ability to work independently and as part of a team
What We Offer:
- Competitive salary and benefits package
- Opportunities for professional growth and development
- A dynamic and collaborative work environment
- Flexible working arrangements, including remote work options
About MAC Clinical Research:
MAC Clinical Research is a global Contract Research Organisation (CRO) with a reputation for delivering high-quality clinical trials. We are committed to serving with honesty and integrity, and we are seeking talented individuals to join our team.
