Clinical Trial Documentation Manager

7 giorni fa


Roma, Lazio, Italia MMS A tempo pieno
Responsibilities

As a Medical Writer at MMS, your key responsibilities include:

  • Evaluating and selecting primary resource materials for clinical study design.
  • Writing and editing clinical development documents, such as protocols, investigator's brochures, and clinical study reports.
  • Maintaining timely completion of writing assignments.
  • Coordinating project facets with clients.
  • Contributing to the production of interpretive guides.
  • Mentoring junior team members.
Requirements

To be successful in this role, you should possess:

  • A minimum of three years of experience in the pharmaceutical industry.
  • At least three to five years of industry regulatory writing and clinical medical writing experience.
  • A degree in a scientific, medical, or clinical discipline.
  • Substantial clinical study protocol experience as lead author.
  • Leadership skills and ability to work under pressure.


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