ProPharma Senior Clinical Writer

Join Pro Pharma as a Senior Clinical Writer, where your expertise will help drive innovative health solutions. This hybrid role focuses on producing high-standard regulatory documents and managing complex writing projects.

We seek an experienced medical writer with at least five years of relevant experience in clinical and regulatory writing. You’ll be responsible for mentoring junior writers while adhering to strict compliance standards and engaging closely with clients. Your ability to foster collaboration and manage multiple projects simultaneously will be crucial.

Key Responsibilities:

• Write and edit essential clinical and regulatory documentation

• Mentor junior writers and ensure adherence to quality standards

• Manage timelines and client expectations effectively

• Conduct quality control reviews and maintain detailed audit trails

• Collaborate with clinical and regulatory teams for accurate outputs

Requirements:

• Bachelor’s degree in a medical or scientific field

• Minimum 5 years of experience in clinical writing

• In-depth knowledge of regulatory submission requirements

• Proficiency in MS Word and document formatting

• Strong communication and project management skills

Utilize your talents to make a difference in healthcare at Pro Pharma.
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