Remote Medical Content Lead / Medical Writing Manager

EVERSANA; Bellprat; Presencial; EUR 60.000 - 85.000; Jornada completa

Descripción de la vacante

EVERSANA is seeking a Medical Content Development Manager / Team Lead to guide medical content development for global clients. The role involves creating scientifically balanced documents and leading content strategy with cross-functional teams.

Applicants should have 2+ years in pharma/Medical Information, strong writing and editing skills, and proficiency with regulatory standards. This is a home-based, full-time position within the EU/UK regulatory framework.

Formación

• Doctorate or MSc in Life Sciences or healthcare.
• Minimum 2 years in pharma/Medical Information or Medical Writing.
• Excellent written, oral, and presentation skills with ability to summarize complex results.
• Proficient editing and experience with PubMed, Ovid, Embase.
• Experience with MS Office, Acrobat and reference management software.
• Strong regulatory knowledge in Medical Information and promotional/non-promotional materials.
• Excellent project management and ability to deliver results.

Responsabilidades

• Support Global Medical Information/Medical Content Development on client engagements.
• Write scientific content for Medical Affairs and Medical Communications (SRDs, FAQs, slides).
• Lead document development from data gathering to MLR review discussions.
• Manage content platforms and annotations as content owner.
• Contribute to SOPs, templates, and guidance documents.
• Stay informed on industry best practices and new technologies.
• Collaborate with writers and teams to deliver projects.
• Participate in client meetings and ensure timely delivery.

Conocimientos

Project Management

Scientific Writing

Communication

Editing

Regulatory Knowledge

Literature Review

Educación

Doctorate or MSc in Life Sciences

Herramientas

MS Office

Adobe Acrobat

EndNote/Mendeley

Descripción del empleo

EVERSANA is seeking a Medical Content Development Manager / Team Lead to guide medical content development for global clients. The role involves creating scientifically balanced documents and leading content strategy with cross-functional teams.

Applicants should have 2+ years in pharma/Medical Information, strong writing and editing skills, and proficiency with regulatory standards. This is a home-based, full-time position within the EU/UK regulatory framework.