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

Dava Oncology is seeking a Clinical 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.

• Maintain 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 for program eligibility and continued support .

• Conduct 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.

• Record 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).

• Act 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.

• Assist 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.

• Track patient eligibility for government health schemes or institutional support programs .
• Assist in documenting required data points to enable continued access to therapies and support.

• Ph. 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)