Clinical Research Coordinator

Brief DescriptionCardiac 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 timelinesPreferred SkillsRequirements or Qualifications:  Degree or Diploma in Practical Nursing 1–2 years of experience in a healthcare or clinical research setting preferred Familiarity with medical records and basic clinical documentation Strong communication and organizational skills Ability to multitask and work independently in a fast-paced environment Basic understanding of Good Clinical Practice (GCP) and clinical research is a plus (training available) and good command over English language and willingness to work on US shifts