Medical Content Development Manager

Medical Content Development Manager, London

Client: EVERSANA

Location: London, United Kingdom

Job Category: -

EU work permit required: Yes

Job Reference: b26a2104ec8e

Job Views: 3

Posted: 26.04.2025

Expiry Date: 10.06.2025

Job Description

Medical Information is a critically important customer-facing function that supports the safe and effective use of pharmaceutical, biopharmaceutical, medical device, and digital therapeutic products by providing timely, scientifically balanced, evidence-based, non-promotional information in response to unsolicited requests from healthcare professionals, patients, caregivers, and payers.

This role involves developing, managing, and providing impactful medical response documents. The position is responsible for client engagements related to medical content development and requires medical information and content experience, including excellent communication skills.

This role can be based in: UK, Ireland, Spain, Italy, Poland, Germany, or Portugal.

Must be legally eligible to work in the EU/UK.

Essential Duties and Responsibilities

1. Support Global Medical Information / Medical Content Development Team on content development projects.
2. Create medical and scientific content such as Scientific Response Documents, FAQs, slide sets, abstracts, posters, and training materials.
3. Manage the client document development process, including content gathering, review, and discussion facilitation at MLR meetings.
4. Work with document management platforms (e.g., Veeva PromoMats) as content owner.
5. Perform scientific data fact checking for documents as needed.
6. Collaborate with global teams on strategy, execution, and communication.
7. Provide guidance to medical writers and content teams.
8. Participate in client meetings.
9. Support SOPs, checklists, templates, and style guides updates.
10. Stay informed of industry best practices and support technology adoption.
11. Work collaboratively across teams.
12. Perform other duties as assigned.

Note: Reasonable accommodations are available for individuals with disabilities.

Expectations

• Deliver client satisfaction.
• Work collaboratively and incorporate feedback.
• Ensure compliance with industry standards.
• Develop high-quality, compliant medical content independently.
• Proactively manage quality issues.
• Travel up to 10-15% may be required.
• Full-time work with flexible scheduling.

All expectations are subject to change and should be performed successfully by the individual.

Qualifications

Minimum Knowledge, Skills, and Abilities:

• Doctorate or MSc in Life Sciences or healthcare or equivalent.
• At least 2 years of experience in pharmaceutical or Medical Information/Communications.
• Excellent written, oral, and interpersonal skills.
• Ability to interpret complex scientific data and communicate effectively.
• Proficiency in Microsoft Office, literature search tools, and reference management software.
• Understanding of regulatory standards in medical information.
• Strong project management skills.

Preferred Qualifications:

• Pharm.D., Pharm.M, MD, or PhD preferred.
• Experience across multiple therapeutic areas.
• Fluent in English and at least one other European language at B2/C1/C2 level.
• Strong analytical, project management, and client management skills.

Additional Information

EVERSANA values diversity and is an Equal Opportunity Employer. We do not ask for payment or personal information during the application process. Beware of fraudulent job offers. Apply via the official 'Apply now' button.

Created on 26/04/2025 by TN UK