Senior Medical Writing Manager

1 day ago


Emelle Alabama, United States Pharmaceutical Research Associates, Inc Full time
Job Summary

We are seeking a highly experienced Senior Medical Writing Manager to join our team at Pharmaceutical Research Associates, Inc. As a key member of our medical writing department, you will be responsible for overseeing the development of high-quality regulatory documents, publications, and other clinical communications.

Key Responsibilities
  • Lead a team of medical writers and editors to ensure timely and high-quality delivery of regulatory documents and publications.
  • Develop and implement departmental strategies to improve efficiency, productivity, and quality of medical writing services.
  • Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and business development, to identify and pursue new business opportunities.
  • Provide expert guidance on regulatory writing, publications, and clinical communications to internal stakeholders and clients.
  • Stay up-to-date with industry trends, regulatory requirements, and best practices in medical writing and clinical communications.
Requirements
  • 5+ years of experience in medical writing, with a minimum of 2 years in a leadership role.
  • Proven track record of leading high-performing teams and delivering high-quality results in a fast-paced environment.
  • Strong knowledge of regulatory writing, publications, and clinical communications, including FDA and ICH guidelines.
  • Excellent communication and project management skills, with the ability to work effectively with cross-functional teams and clients.
  • Bachelor's degree in a life science or related field.
What We Offer

At Pharmaceutical Research Associates, Inc., we offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development. If you are a motivated and experienced medical writing professional looking for a new challenge, please submit your application.



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