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SJ

Swarali Prasad Javdekar

Clinical Research Coordinator · GCP-trained

Kolhapur, Maharashtra, India

@swarali_javadekar

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About

Clinical Research Coordinator with site-level exposure to clinical trial coordination, study documentation, investigational product accountability, and ethics/regulatory documentation. Trained in Good Clinical Practice (GCP) with experience supporting protocol compliance and study-team communication.

Experience

  • Clinical Research Coordinator (CRC)
    Trial Pulse Clinical Research
    Aug 2026 – Present

    Assist with day-to-day clinical trial coordination and communication among the Principal Investigator, study team, CRA/CRO, and site personnel; maintain and organize study documentation, source records, essential documents, and site files; support informed-consent documentation, participant visit coordination, investigational product accountability records, temperature logs, packing lists, and shipment-temperature/data-logger documents; support preparation and filing of Ethics Committee submissions and other study/regulatory documents; assist with review of study data and follow-up of EDC/IRT queries or discrepancies; follow GCP principles, protocol requirements, confidentiality practices, and site standard operating procedures.

Education

  • P.G. Diploma in Clinical Research with Ethics
    Clinical Research Institute, Nagpur
    Clinical Research with Ethics · 2026
  • B.Pharm
    ASPM College of Pharmacy, Vaibhavwadi, Sindhudurg
    Pharmacy · 2026
  • D.Pharm
    ASPM College of Pharmacy, Vaibhavwadi, Sindhudurg
    Pharmacy · 2023

Skills

3 to 6 months 3 to 6 months A few months of practice with it.
Informed Consent Regulatory Affairs Protocol Compliance Documentation Management Clinical Trial Coordination

Tools / apps / platforms

<3 months <3 months Just getting started - under three months. This is also what shows when a level has not been set.
GCP

Courses & certifications

  • Good Clinical Practice (GCP) · NIDA Clinical Trials Network · 2026

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