Head regulatory affairs
ChennaiRandstad
...Medical Writing, Pharmacovigilance, and Data Management teams to ensure regulatory requirements are met at every stage. Provide regulatory guidance in protocol design, informed consent, and clinical study documentation. Qualifications and ExperienceEducation: Advanced degree (PharmD, PhD, MD, or MSc) in Life Sciences, [...]
Category Education, Training, & Library
30+ days ago in Randstad