{"@context":"https://schema.org","@type":"JobPosting","title":"Clinical Trails Associate","description":"

Job Summary

The Clinical Trials is responsible for coordinating and managing clinical research studies in compliance with protocol requirements, ICH-GCP guidelines, regulatory authorities, and hospital policies. The role ensures smooth execution of clinical trials while maintaining participant safety and data integrity.

Key Responsibilities

Coordinate and manage clinical trial activities from initiation to completion.
Screen, recruit, and schedule study participants as per protocol.
Obtain informed consent and ensure ethical conduct of studies.
Coordinate with Principal Investigators, sponsors, CROs, and hospital departments.
Maintain study documentation, source documents, and regulatory files.
Collect, record, and manage clinical trial data accurately.
Report adverse events and protocol deviations as per regulatory requirements.
Ensure compliance with ICH-GCP, ethics committee, and applicable regulatory guidelines.
Prepare for sponsor, regulatory, and internal audits.
Maintain confidentiality of patient and study information.

Qualifications

Pharm.D, B.Sc./M.Sc. Life Sciences, Nursing, or equivalent.
Certification in Clinical Research or GCP is preferred.

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