Cardiac research division of a US firm is in association with Hiworth Solutions Pvt Ltd in Technopark is looking for a Clinical Research Coordinator. In this role, you will be an essential part of our mission to deliver cutting-edge cardiac therapies through clinical trials. You’ll support physicians and research staff by managing daily study activities, coordinating patient visit data nd details, and ensuring protocol compliance in all research-related tasks.
Key Responsibilities:
Assist in coordinating all aspects of clinical trial activities, including patient scheduling, follow-up, and communication
Obtain informed consent from study participants and provide education regarding study procedures
Collect and accurately document clinical data in source records and electronic data capture (EDC) systems.
Monitor and report patient safety data, including adverse events
Maintain organized and complete regulatory documentation and subject files
Assist with IRB submissions, amendments, and study start-up activities
Prepare for and participate in monitoring visits and sponsor audits coordinate the collection and process of blood or lab specimens in accordance with study protocols
Accurately enter patient and study data into electronic data capture (EDC) systems
Review and verify data from source documents to ensure completeness and accuracy
Organize, maintain, and update clinical trial files, logs, and documentation
Assist research staff with tracking visit schedules, reports, and study milestones
Respond to data queries from sponsors or monitors in a timely and professional manner
Support regulatory filings and assist in maintaining study binders and audit readiness
Collaborate with team members to ensure data is collected and entered within protocol-specified timelines