Medical Writer

Job Description:
In this role, incumbent will be expected to provide Medical Writing leadership for clinical development, registrational, and LCM programs. Serves as lead Medical Writer for key programs. Coordinates medical writing support for programs with internal and contract writers.
Additionally, must posess the ability to guide and assists medical writers in the writing of documents that are components of clinical/ regulatory approval applications for new biologics or NME applications.

Documents include: Sections of clinical trial applications, Annual Reports, and BLA/NDAs, Protocols and Protocol Amendments, Model Informed Consents, Model Privacy Consents, Investigator Brochures, Clinical Study Reports, and Expert Reports and other documents as appropriate.
Additional

skills:

• 
  must be a strong technical leader, manage with excellent scientific, strategic and customer focused leadership.
  Partner with Clinical Operations and R&D team members to ensure completion of high quality, timely, clinical documentation.
  Expected Qualification: Masters or PhD in biology or related discipline.
• Equivalent combination of education and experience considered.
• 7+ years of related experience in biotech or pharmaceutical environment.
• Must have strong scientific and operational background.
• At least 3 years of experience managing staff.
  All your information will be kept confidential according to EEO guidelines.