Study Start-Up Coordinator(Clinical Trials)
Minerva Research Solutions
Date: 8 hours ago
City: Remote
Contract type: Full time
Remote
About Minerva Research Solutions
Minerva Research Solutions is a leading Clinical Trial Management and Support organization dedicated to advancing global healthcare through innovation, operational excellence, and regulatory compliance. We partner with biotech, pharmaceutical, and healthcare organizations to deliver integrated clinical trial support services across the full study lifecycle.
At Minerva, we are committed to maintaining the highest standards of quality, compliance, and efficiency while enabling breakthrough therapies to reach patients faster.
The Study Start-Up Coordinator is responsible for overseeing study startup timelines and coordinating cross-functional activities to ensure all prerequisites for Site Initiation Visits (SIV) and site activation are completed efficiently and on schedule. This role serves as the central coordination point between departments to monitor dependencies, mitigate delays, and ensure operational readiness for successful study activation.
Key Responsibilities
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Minerva Research Solutions is a leading Clinical Trial Management and Support organization dedicated to advancing global healthcare through innovation, operational excellence, and regulatory compliance. We partner with biotech, pharmaceutical, and healthcare organizations to deliver integrated clinical trial support services across the full study lifecycle.
At Minerva, we are committed to maintaining the highest standards of quality, compliance, and efficiency while enabling breakthrough therapies to reach patients faster.
The Study Start-Up Coordinator is responsible for overseeing study startup timelines and coordinating cross-functional activities to ensure all prerequisites for Site Initiation Visits (SIV) and site activation are completed efficiently and on schedule. This role serves as the central coordination point between departments to monitor dependencies, mitigate delays, and ensure operational readiness for successful study activation.
Key Responsibilities
- Study Start-Up Planning & Coordination
- Track study startup timelines aligned with project milestones and activation goals
- Coordinate cross-functional activities required for study initiation
- Ensure all prerequisites for Site Initiation Visits (SIVs) are completed within timelines
- Cross-Functional Alignment
- Coordinate with Regulatory, QA, Marketing, Finance, and Clinical teams to track deliverables and dependencies
- Identify bottlenecks impacting startup timelines and escalate risks appropriately
- Facilitate communication between departments to maintain alignment on project objectives and deadlines
- Timeline & Milestone Tracking
- Monitor progress against startup timelines using internal tracking tools and dashboards
- Maintain accurate startup reports and provide regular status updates to stakeholders
- Proactively address delays and support implementation of corrective actions
- SIV Readiness & Site Activation
- Ensure all regulatory, operational, and documentation prerequisites are fulfilled prior to SIV
- Confirm site activation requirements are completed and appropriately documented
- Support smooth coordination leading to successful site activation
- Risk Management
- Identify potential risks impacting study startup activities and timelines
- Collaborate with stakeholders to develop mitigation and contingency strategies
- Monitor ongoing startup risks and ensure timely resolution of issues
- Bachelor’s degree in Medical Sciences, Life Sciences, Pharmacy, or a related field
- MBBS, BDS, or Pharm-D candidates will be preferred
- Minimum 1 year of experience in clinical research or study startup coordination
- Familiarity with regulatory requirements, clinical trial startup processes, and site activation workflows
- Experience working with cross-functional teams in a fast-paced environment is preferred
- Strong project coordination and organizational skills
- Excellent communication and stakeholder management abilities
- Ability to manage multiple timelines and priorities effectively
- Strong problem-solving and proactive risk management capabilities
- Attention to detail with a quality-focused mindset
- Proficiency in reporting and startup tracking tools
- On-time completion of study startup milestones
- Adherence to SIV and site activation timelines
- Number of delays/escalations successfully mitigated
- Effectiveness of cross-functional coordination and communication
- Accuracy and timeliness of startup reporting and tracking
- Competitive compensation with performance-based rewards
- Comprehensive medical insurance
- EOBI retirement benefits
- Structured Learning & Development pathways, including certifications and career mobility
- Paid annual, medical, and casual leave
- Mental well-being and employee support programs
- Inclusive, collaborative, and growth-driven work culture
- Internal recognition & employee engagement initiatives
- Modern digital tools and a technology-forward workplace
- Transportation allowance for staff
- Family-supportive policies, including parental leave
- Opportunities to contribute to community and social impact programs
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