Clinical Research Associate (CRA) – Patient Support & Outcomes Tracking

About the RoleDava Oncology is seeking aClinical Research Associate (CRA)to support patient-focused programs in collaboration with government medical colleges and public hospitals across India. This role is not a site-monitoring CRO role, but a programmatic CRA position focused on structured patient data capture, longitudinal follow-up, treatment compliance, safety monitoring, and outcomes tracking for patients receiving advanced therapies (including biologics). The CRA will work closely with treating physicians, program coordinators, and internal teams to ensure high-quality data, consistent follow-up, and accurate documentation that supports patient care, reporting, and access to support schemes.Key ResponsibilitiesPatient Data Management & DocumentationMaintain accurate, structured patient records for all supported patients (demographics, diagnosis, treatment, follow-up). Ensure completeness of clinical data including: Indication and eligibility Baseline assessments Concomitant medications Lab and imaging summaries (as provided by treating sites) Track documentation required forprogram eligibility and continued support .Follow-up, Compliance & Outcomes TrackingConduct scheduled follow-ups (telephonic / virtual / site-based) to assess: Treatment adherence and compliance Clinical response and efficacy (as reported by clinicians) Adverse events and side effects Changes in concurrent treatments Flag deviations, missed doses, or safety concerns to the program team and treating physician.Safety & Adverse Event ReportingRecord and track adverse events and serious adverse events in a structured format. Ensure timely escalation of safety signals to internal medical and program leadership. Maintain consistency with internal SOPs and basic pharmacovigilance principles (training will be provided if needed).Physician & Site CoordinationAct as a primary coordination point with treating physicians and hospital teams for: Follow-up data collection Missing documentation Treatment continuation confirmations Support efficient communication between Dava Oncology and partner institutions.Program Reporting & InsightsAssist in generating periodic summaries and dashboards on: Patient numbers and demographics Treatment continuation and discontinuation Compliance trends Safety observations Support internal reviews to identify gaps in follow-up, documentation, or patient access pathways.Government Schemes & Support EligibilityTrack patient eligibility forgovernment health schemes or institutional support programs . Assist in documenting required data points to enable continued access to therapies and support.QualificationsPh. D / MSc (Life Sciences, Pharmacy, Biotechnology, Nursing) MBBS / MD candidates welcome but not mandatory Prior experience as: Clinical Research Associate Familiarity with: Biologic or specialty therapies (rheumatology, oncology, immunology preferred)

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