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Clinical Evaluation Report Specialist
2 months ago
We are seeking a highly skilled medical writer to join our team at Publicis Groupe UK. As a Clinical Evaluation Report Writer, you will be responsible for translating complex scientific and clinical information into clear and concise documents for our clients in the healthcare and pharmaceutical industries.
Key Responsibilities:- Prepare and edit clinical study protocols, clinical study reports, investigator brochures, and other regulatory documents for submission to health authorities.
- Ensure that these documents comply with regulatory guidelines and standards.
- Communicate complex scientific and medical information to various audiences, including healthcare professionals, regulatory agencies, and the public.
- Collaborate with cross-functional teams to compile and write sections of regulatory submissions, such as New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), and Investigational New Drug (IND) applications.
- Native French speaker with expertise in healthcare and pharmaceutical industries.
- Excellent writing and communication skills, with the ability to convey complex scientific information in a clear and concise manner.
- Strong understanding of regulatory guidelines and standards.
- Ability to work independently and as part of a team.
- A dynamic and supportive work environment.
- Opportunities for professional growth and development.
- A competitive salary and benefits package.
We are an equal opportunities employer and welcome applications from all sections of society. If you are a motivated and experienced medical writer looking for a new challenge, please submit your application.
