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Clinical Evaluation Report Specialist
2 months ago
We are seeking a 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 pharmaceutical industry.
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 in a clear and understandable manner for diverse audiences, including healthcare professionals, patients, and the general 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.
- Strong writing and editing skills, with the ability to communicate complex scientific and medical information in a clear and concise manner.
- Experience in regulatory document preparation and submission.
- Ability to work independently and collaboratively 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.
