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 reliable 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

📌 Clinical Research Associate (Pollachi)
🏢 Ardor Biomed (I
📍 Pollachi