Role Overview

About the role. eteraflex connects is building a Clinical Science Pod an embedded, accountable unit of clinical and scientific specialists who plug into sponsors oncology programs and our own India trials. The Clinical Science Associate is a deliberately hybrid role: you will train across site monitoring, site-side coordination, and medical/scientific oversight support, so that you understand both the medicine and the operations of a clinical trial. You will not be a single-function CRA or a single-function coordinator you will become a versatile clinical science operator who can move between India sites and embedded sponsor support as programs demand.

What youll do (responsibilities)

Site monitoring (CRA-track)

Conduct and support site monitoring visits site qualification, initiation, routine monitoring, and close-out at Indian oncology centres.

Perform source data verification and review, confirming trial data against source records for accuracy and completeness.

Track site-level enrolment, identify screen-failure and recruitment gaps, and escalate risks to the Pod Lead.

Monitor protocol compliance and valuable clinical practice (GCP) at sites; document and follow up on deviations.

Site coordination investigator support (CRC / PI-support track)

Support investigators (PIs) and site coordinators (CRCs) on protocol execution, eligibility screening, and patient scheduling.





Assist sites with regulatory and ethics-committee documentation, informed consent processes, and trial master file readiness.

Coordinate biomarker and tissue-sample logistics with sites and central labs retrieval, handling, and chain-of-custody.

Act as a working bridge between the site and the sponsor/Pod, so issues are caught and resolved early.

Medical scientific support (CMO-support track)

Support the Pods Medical Scientific Lead and physicians with protocol-query resolution, eligibility clarifications, and medical-data review.

Prepare materials for and participate in safety reviews and safety meetings (DSMB/DMC interactions, AE/SAE tracking). Note: medical monitoring and safety adjudication decisions are made by a qualified physician on the Pod; associates support and document these, they do not sign them off.

Contribute to gap analyses of underperforming sites diagnosing why enrolment or quality is lagging and helping shape corrective actions.

Build therapeutic and scientific fluency in the Pods oncology focus areas, so site and sponsor conversations are credible.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Study Coordinator (Warangal)
🏢 TK-Chain
📍 Warangal