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Strong fit if you already monitor independently, like variety across sponsors, and can operate from Poland with site travel and rigorous documentation. Thin public people-sentiment data; judge culture from interviews and the hiring team.
As a CRA II – Multi Sponsor at Syneos Health India Private Limited supporting Poland-based work, a typical day centers on multi-sponsor monitoring: reviewing site readiness, source data verification, query resolution, and protocol/GCP compliance across several sponsors’ trials. Expect remote report writing, CTMS updates, PI/site calls, and on-site or remote visits for enrollment, safety follow-up, and CAPA tracking—not a fixed single-study desk role.
Prioritize ICH-GCP fluency, multi-protocol prioritization, SDV/risk-based monitoring habits, clear site coaching, and clean visit reporting. No certification catalog was provided for costed study paths.
The listing marks remote as no; expect Poland-based work with site-facing monitoring as required by study plans.
You support more than one sponsor’s trials, so SOPs, timelines, and systems can differ by study—organization and prioritization matter.
India people-operations leadership coverage and broader CRO/India CRO market pieces; trial/regulatory mentions also appear in medical press—read primary sources, not ratings sites.
Website: syneoshealthindiaprivate.com
Public cache only — not an employee review.
CRA II - Multi Sponsor | Syneos Health India Private Limited | Poland About This Position This position at Syneos Health India Private Limited in Poland is for a CRA II - Multi Sponsor. As a member of the Clinical Solutions team, you will be involved in site qualification and other critical activities to support drug development projects. What You'll Do Perform site qualification visits and ensure sites meet regulatory requirements. Support clinical trial operations by managing site relationships and ensuring compliance with study protocols. Contribute to the overall success of clinical trials through effective communication and collaboration with stakeholders. Participate in data management activities, including monitoring and reporting. Requirements Experience as a CRA or similar role within the pharmaceutical industry. A strong understanding of Good Clinical Practices (GCP) and regulatory requirements. Excellent communication and interpersonal skills to interact with site personnel, sponsors, and other stakeholders. Proficiency in Microsoft Office Suite for documentation and report preparation. Why Join Syneos Health India Private Limited At Syneos Health, we are committed to building an inclusive culture where you can authentically be yourself. Our purpose - Driven to Deliver - captures the passion of our colleagues to shape solutions that have the potential to dramatically impact someone’s life. We invest in our people through career development and progression, supportive line management, technical training, peer recognition, and a total rewards program. Join us as we bring together smart colleagues from across the world to drive the future of healthcare and define the pace of patient progress. Apply Today To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. We look forward to hearing from you!
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