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Generalist data role, metro Bangalore, and broad non-niche requirements drive high competition.
Requires clinical trials and laboratory-specific experience and systems, making background fit highly industry-specific.
Explicit clinical-lab and project-management years plus domain-specific systems increase shortlisting strictness.
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Serve as the primary contact for sponsors on all matters related to ICON Laboratory Services for clinical studies.
Manage clinical study setup, coordination, and communication including entering protocol data into systems and maintaining documentation.
Monitor study progress, budget, and shipments while providing regular updates and representing ICON at client meetings.
Bachelor's degree in Science, Business, or a related field.
Minimum 2 years experience in clinical laboratory, clinical trials, or customer/account management in life sciences.
Minimum 1 year Project Management experience in service areas supporting clinical trials (e.g., IVRS, Clinical Supplies, Medical Imaging).
Proficient with Microsoft Word, Excel, and PowerPoint; Legal right to work in India.
Experienced managing coordination and communication of clinical studies in a laboratory or clinical trial environment.
Skilled in project management with ability to handle cross-functional study documentation and client interactions.
Comfortable working in a hybrid office-based setup with strong system and process adherence.