Senior Medical Writer — Clinical Documentation Leader

Parexel; Paris; Hybride; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A global biopharmaceutical services company is seeking a Medical Writer to support clinical documentation and regulatory submissions. The ideal candidate should have a Bachelor's in Life Sciences, significant experience in medical writing, and strong interpersonal skills. This role involves authoring Clinical Study Reports, managing documentation quality, and liaising with clients. The company offers a competitive package in a supportive, team-oriented environment promoting professional growth.

Prestations

Competitive base salary

Private healthcare

Career development opportunities

Qualifications

• 5+ years of medical writing experience at a senior level.
• Understanding of clinical research and drug development process.
• Experience with clinical study reports and regulatory documentation.

Responsabilités

• Author clinical documents for regulatory submission.
• Ensure quality control of documentation.
• Manage projects and client relationships.

Connaissances

Excellent interpersonal skills

Verbal and written communication skills

Ability to manage multiple tasks

Team leadership skills

Fluent English communication

Formation

Bachelor's degree in Life Sciences or Health Related Sciences

Outils

MS Office (Word)

SharePoint

Description du poste

A global biopharmaceutical services company is seeking a Medical Writer to support clinical documentation and regulatory submissions. The ideal candidate should have a Bachelor's in Life Sciences, significant experience in medical writing, and strong interpersonal skills. This role involves authoring Clinical Study Reports, managing documentation quality, and liaising with clients. The company offers a competitive package in a supportive, team-oriented environment promoting professional growth.