Clinical Research Coordinator

7 days ago

Delhi, Delhi, India ProClin Research Private Limited Full time

Company Description

ProClin Research Private Limited specializes in delivering high-quality services across all phases of drug development. From start-up to the completion of final study reports, the company monitors performance and ensures adherence to timelines and budgets. ProClin Research is dedicated to providing cost-effective solutions while maintaining an agile, hands-on approach with operational teams working closely with clinical sites. By leveraging various outsourcing models, ProClin Research offers flexibility and builds strong client relationships as a trusted single-source provider.

Role Description

This on-site contract role is based at Multiple Locations . The Clinical Research Coordinator will manage the day-to-day operations of clinical research studies, including obtaining informed consent, coordinating participant enrollment, ensuring adherence to study protocols, and maintaining study-related documentation. The role involves closely working with clinical teams, reviewing clinical trials, and ensuring compliance with regulatory and ethical guidelines.

Qualifications

  • Experience with Informed Consent processes and a thorough understanding of research protocols
  • Strong background in Clinical Research and familiarity with overseeing Clinical Trials
  • Ability to effectively collaborate with clinical teams and maintain detailed documentation
  • Possess a Bachelor's degree or higher in a related field
  • Excellent organizational and communication skills
  • Familiarity with regulatory requirements and GCP (Good Clinical Practice) guidelines
  • Previous experience in managing clinical sites is a plus

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