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Metro location, mid-level experience band, and strong global CRO brand increase candidate competition.
Requires clinical research and regulatory expertise, limiting transferability across industries.
Explicit 3.5–4 years clinical research plus regulated Veeva/TA expertise makes shortlisting stringent.
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Act as Single Point of Contact (SPOC) for site activation activities in assigned studies, coordinating between investigative sites, Site Activation Manager, and project teams.
Perform start-up and site activation tasks including preparation, review, and distribution of regulatory and contractual documents ensuring adherence to SOPs, project timelines, and quality standards.
Maintain accuracy of project-specific data in internal systems (e.g., Veeva, COSMOS), track site performance, provide feedback, and support project planning including contingency measures.
3.5 to 4 years of clinical research experience (or equivalent combination of education, training, and experience).
Preferably at least 1 year of study start-up experience.
Experience with site activation processes, regulatory document preparation, and internal system management (Veeva/COSMOS).
Work Experience Required: 3.5 to 4 years clinical research; notice period: Not explicitly mentioned in the JD.
Experienced in clinical study start-up with demonstrated ability to manage site documentation and activation within regulatory and project frameworks.
Skilled at coordinating multiple stakeholders including sites, project management, and sponsors as needed, acting as effective SPOC.
Detail-oriented in compliance, quality control, and project tracking with a focus on adhering to SOPs and timelines.