Clinical Research Medical Writer

Step into a Clinical Research Medical Writer role focused on developing high-quality regulatory documents. Your expertise will guide collaboration with scientists and external experts, driving the accuracy of research submissions.

This role demands a solid 3-5 years of medical writing experience, particularly in producing protocols, informed consent forms, and clinical study reports. You will ensure that all deliverables meet established standards while tracking their progress and managing timelines of multiple projects.

Key Responsibilities:

• Lead the production of regulatory documentation across projects

• Collaborate with technical specialists for content accuracy

• Manage projects by tracking deliverable timelines

• Participate in quality reviews for author contributions

• Support editing and proofreading of study-related documents

Requirements:

• Minimum undergraduate degree, advanced degrees preferred

• 3-5 years of related medical writing experience

• Knowledge of GCP, GDPR, and HIPAA regulations

• Proficient in End Note/reference software for citation management

• Strong communication skills, with an ability to work diplomatically

Use your medical writing talent to support vital clinical research initiatives in this resourceful position.