Job Description
Under the direction of Medical Writing management, the Senior Quality Control Associate provides a thorough quality control (QC) review of regulatory documents and medical communications to support all phases of product development. These documents include, but are not limited to, clinical study reports, study protocols, subject safety narratives, informed consent documents, investigator’s brochures, clinical and nonclinical sections of regulatory submissions, and manuscripts.
Veristat is proud to provide exceptional services to our clients, assisting in the successful development of innovations that improve and save lives. We are equally proud to recruit, develop and retain the best and the brightest talent across a variety of business functions to make that happen.
About Veristat
Veristat is a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.