Medical Monitor Team Leads/Asst Manager

As a Protocol Review Specialist, you will play a crucial role in the clinical trials process. Your responsibilities will include reviewing protocols, responding to queries and clarifications from EC/IRB, answering medical questions, attending drug safety meetings, reviewing AE/SAEs, and providing protocol training to site staff, CRAs, etc. during investigator meetings. Key Responsibilities: - Reviewing protocol and providing suggestions to enhance the process - Responding promptly to queries/clarifications from EC/IRB - Addressing medical questions from sites or project teams effectively - Attending important drug safety meetings and external meetings - Thoroughly reviewing and documenting AE/SAEs - Conducting comprehensive protocol training for site staff, CRAs, etc. during investigator meetings Qualifications Required: - Prior experience in clinical trials is essential - Proficiency in handling SAES will be advantageous - Ability and willingness to actively participate in external meetings Please note that the company operates within the ITES/BPO/KPO industry, with a strong focus on the pharmaceutical sector. This role is categorized under Life Sciences and Pharma. If you have any further questions or need clarification, please feel free to reach out. Job Code - GO/JC/20991/2025 Recruiter Name - HariharanA,