Job Description

Ardor Biomed is seeking a Clinical Research Associate (CRA) to support ongoing clinical trial process. This role is a site-monitoring role focused on structured patient data capture, treatment compliance, safety monitoring, and outcomes tracking for patients receiving specific treatments.

The CRA will work closely with 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 Responsibilities

Patient Data Management & Documentation

Maintain accurate, structured patient records for all supported patients (demographics, diagnosis, treatment, follow-up). Ensure completeness of clinical data including : Inclusion and exclusion criteria Indication and eligibility Baseline assessments Lab and imaging summaries (as provided by treating sites) Track documentation required for program eligibility and continued support .
Follow-up, Compliance & Outcomes Tracking

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.
Safety & Adverse Event Reporting

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).
Physician & Site Coordination

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.
Program Reporting & Insights

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.
Qualifications

Ph. D / MSc (Life Sciences, Pharmacy, Biotechnology) Prior experience as Clinical Research Associate preferrable but not mandatory.
Job Type: Full-time

Pay: ?15,000.00 - ?25,000.00 per month

Work Location: In person