Medical Writer - Regulatory Submissions

Zest Scientific is partnered with a global-leading pharmaceutical company expanding their internal medical writing function across numerous levels (Associate, Senior, Principal).

If you’re a Medical Writer with exposure to drug development regulatory submissions and are looking for a new challenge then this could be the one for you.

The Candidate:

• Experienced Medical Writer with exposure to regulatory submissions.
• Proven experience producing high-quality scientific writing.
• Highly organised; able to achieve goals, working to strict timelines.
• Strong communication; working effectively on cross-functional teams, creating collaborative relationships.

The Role:

• Leading cross-functional teams in content preparation; with a high level of key stakeholder interaction.
• Pivotal strategic input in both functional and cross-functional teams regarding content development.
• Keep up-to-date with medical, scientific, and regulatory knowledge relevant to the assigned therapeutic areas.

The Opportunity:

• Global-leading pharmaceutical company that is a pioneer in research-focused healthcare.
• People-oriented culture with continuous opportunities for personal and professional development.
• State-of-the-art headquarters to be utilised through hybrid working (ideally 2 days a week onsite).

Remunerations:

• Our client is committed to securing the services of the right candidate and is flexible with regards to the remuneration package available. Zest Scientific is working to a strict deadline so in order to be considered for this opportunity please apply now and your application will be reviewed immediately.

Contact: Caitlyn Lindley
Email: caitlyn.lindley@zestbusinessgroup.com
Telephone: 0114 287 0351