Roles & Responsibilities
• Manage end-to-end clinical trial project activities from initiation to close-out
• Coordinate with Sponsors, CRO partners, investigators, and cross-functional teams
• Develop and track project timelines, milestones, and deliverables
• Ensure compliance with ICH-GCP, SOPs, and applicable regulatory guidelines
• Monitor project progress, risks, and issues and implement mitigation strategies
• Support site start-up, monitoring, and close-out activities
• Prepare and review project-related documentation and reports
• Ensure effective communication across all stakeholders
• Support budget tracking and resource coordination for assigned studies
Qualification
• M.Pharm
• B.Pharm
Experience
• Prior exposure as a Project Manager or project coordination role preferred
• Experience in Biosimilars and/or small molecule clinical trials desirable
• Experience from Sponsor or CRO platform preferred
Skills
• Strong project coordination and organizational skills
• Good understanding of clinical trial processes and regulations
• Effective communication and stakeholder management abilities
• Ability to manage multiple tasks and meet timelines
• Attention to detail and problem-solving skills
About the Organization
Jeevan Scientific Technology Limited is a global life sciences services organization offering end-to-end solutions in clinical research, regulatory affairs, medical writing, pharmacovigilance, and project management, supporting pharmaceutical and biotech companies across the clinical development lifecycle.
Unlock refined AI insights.