Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug
Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level
Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level