Principal Medical Writer

Position: Principal Medical Writer Hybrid Role
Join Pro Pharma as a Principal Medical Writer in a hybrid setting that champions patient health and innovation. This full-time position focuses on producing regulatory documents and leading project teams.

With experience spanning over 25 years, Pro Pharma partners with biotech and pharmaceutical companies to advance scientific breakthroughs. As a Principal Medical Writer, you will independently manage key deliverables, ensuring compliance with ICH standards while mentoring junior writers and overseeing quality control processes.

Key Responsibilities:

• Lead the writing and editing of complex regulatory documents

• Interact with clients to manage project timelines efficiently

• Supervise quality control reviews and audits

• Collaborate with clinical experts to finalize submissions

• Assist in departmental initiatives and continuous improvement

Requirements:

• Bachelor’s degree or higher in a relevant field

• At least 7 years in clinical and regulatory writing

• Advanced knowledge of submission guidelines and regulations

• Strong MS Word skills, especially with complex documents

• Excellent project management and communication abilities

Bring your extensive medical writing experience to Pro Pharma and help shape the future of patient care.
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