
Principal Oncology Trials Manager
1 day ago
Overview
A Clinical Trial Lead plays a pivotal role in the successful execution of clinical trials, ensuring seamless site activation, regulatory compliance, and timely delivery. We are seeking an experienced professional to lead Phase I, II, and III oncology studies at key national institutions in India.
The ideal candidate will have a strong working knowledge of GCP, ICH, and CDSCO guidelines, as well as excellent interpersonal, communication, and problem-solving skills.
Responsibilities- Lead clinical operations and site-level engagement for assigned Phase's studies in India
- Manage relationships with Principal Investigators (PIs), CRCs, and Institutional stakeholders at government hospitals
- Oversee timely and compliant PSSV, site initiation visits (SIV), patient recruitment, and data collection
- Ensure study milestones are met, including First Patient First Visit (FPFV) and clean database targets
- Collaborate with sponsor teams, regulatory consultants, and third-party vendors to streamline dossier submissions and audit readiness
- Coordinate regulatory submissions and ethics committee (EC) approvals; ensure alignment with CDSCO, ICMR, and local EC timelines
- Conduct ongoing risk assessment and drive mitigation strategies across sites
- Provide oversight to field CRAs and monitor site compliance
To be successful in this role, you should possess:
- Bachelor's degree in life sciences or related field; advanced degree preferred
- Minimum 6-8 years of clinical research experience with at least 3 years in an independent CTM role
- Demonstrated experience in oncology or immunotherapy trials, preferably with exposure to AIIMS or government research centers
- Strong working knowledge of GCP, ICH, and CDSCO guidelines
- Proven track record managing multi-site studies and remote monitoring teams
- Excellent interpersonal, communication, and problem-solving skills
- Proficiency in CTMS, EDC, and eTMF systems is a plus
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