Clinical Trial Incharge / Site Manager

As a Clinical Trial Incharge/Site Manager in the Research Department at American Cancer Institute & Hospital in Hyderabad, your role involves coordinating, managing, and monitoring clinical trials in the oncology research department while ensuring compliance with GCP, ICMR, and regulatory guidelines. Key Responsibilities: - Oversee the day-to-day conduct of clinical trials. - Coordinate with investigators, CROs, and sponsors. - Ensure protocol adherence, regulatory submissions, and IEC approvals. - Supervise patient recruitment, consent, and data collection. - Maintain documentation, drug accountability, and trial master files. - Prepare for audits and monitoring visits. - Manage trial budgets and site logistics. - Train and guide research staff on GCP and SOPs. Qualifications: - MBBS/M.Pharm/M.Sc (Life Sciences/Clinical Research)/MD Pharmacology. - 10-15 years of experience in clinical trial management, preferably in oncology. In addition to the outlined responsibilities and qualifications, the ideal candidate should have: - Strong knowledge of GCP, ICMR, and Schedule Y. - Excellent communication and coordination skills. - Proficiency in MS Office and EDC/CTMS systems. - Detail-oriented with leadership ability. This is a full-time, on-site position with a salary as per institutional norms. If you are passionate about research, cancer, clinical trials, oncology, and possess the required qualifications and skills, we encourage you to apply for this challenging role.,