Medical Writer

My client is seeking a medical writer experienced in drafting manuscripts and protocols for pharmaceutical clients. This is a remote position which gives you the opportunity to work on regional studies.

Job Responsibilities:

1. Draft and review regulatory medical writing documents, including manuscripts and clinical trial protocols.
2. Contribute to impactful scientific articles in Oncology, collaborating on high-impact projects.
3. Work on studies across regions, including the US and Europe.
4. Ensure documents meet regulatory standards (ICH-GCP).
5. Develop side decks to explain clinical trial data results and analysis in detail.

Job Requirements and Perks:

1. Remote position, but talent must be based in APAC.
2. Bachelor’s or Master’s Degree in Lifesciences, Medicine, Pharmacy, or any related field (PhD is ideal).
3. CMPP certification will be advantageous.
4. Strong understanding of the clinical research process and regulatory guidelines.
5. Experience in writing Oncology articles.

Interested applicants, please click Apply to this post, and I will follow up with you accordingly.

Gina Yeo

Senior Recruitment Manager

CEI: R1660520 | Licence No: 19C9622 |