ProPharma is seeking a Senior or Principal Medical Writer with proven early phase experience to support a top‑tier pharmaceutical client. Based in the UK or Ireland, you will author and edit clinical, safety and regulatory documents across multiple programs, ensuring quality, accuracy and timely delivery.
You will lead project communications, coordinate with cross‑functional teams, mentor junior writers, and maintain compliance with ICH guidelines, FDA expectations, and client templates.
#J-18808-LjbffrSenior Medical Writer — Clinical & Regulatory Leader employer: ProPharma
ProPharma is an exceptional employer that fosters a dynamic and collaborative work culture, ideal for those looking to thrive in the fast-paced world of commercial finance. Employees benefit from comprehensive professional development opportunities, working alongside industry leaders while contributing to impactful projects. Located in a vibrant area, ProPharma offers a unique blend of career growth and a supportive environment, making it a rewarding place to advance your career.
