Syneos Health Medical Writer Jobs in Clinical Trial Team
Syneos Health is a growing and evolving biopharmaceutical industry leader, with a global team dedicated to improving patients’ lives. We believe in creating a work environment where everyone can thrive, and we take pride in fostering a culture of inclusivity and innovation.
Job Title: Principal Medical Writer (CTT)
Job Summary
The Principal Medical Writer in Clinical Trial Disclosure plays a crucial role in handling complex scientific and medical information for Syneos Health’s global clients. This role involves authoring, quality assurance, and compliance with regulatory requirements.
Job Responsibilities
- Authoring and quality assurance of project activities
- Marking/QC/Review of clinical study documents for regulatory submissions
- Systematic quality control checks of documents
- Assisting in training and mentoring team members
Qualifications
- We are looking for a candidate with at least 8 years of experience as a medical writer, familiar with CTT/redactions/anonymization of clinical documents for various regulatory standards.
- A minimum of a scientific graduate degree in life sciences.
- Good knowledge of regulatory requirements or guidance pertinent to the service line.
- Good understanding of clinical development processes including principles of clinical study operations and ICH-GCP guidelines. Clear written and verbal communication skills
- Good knowledge of basic computer applications, e.g. MS Word/ PowerPoint/ Excel, will be required.
About Syneos Health
Over the past 5 years, Syneos Health has worked on numerous FDA-approved drugs and EMA-authorized products, making a significant impact in the healthcare industry. Join us in our mission to drive innovation and improve patient outcomes.
