Clinical Research Associate

6 days ago

Vellore, Tamil Nadu, India Dozee Full time ₹ 3,00,000 - ₹ 9,00,000 per year
Job Title: Research Associate (Contract, On-site at CMC Ranipet) Location: CMC Ranipet, Tamil Nadu Experience: 0-1 years Job Type: Contract-based, On-site (Day & Night Shifts Required) Contract Duration: 6+ months Job Description: We are seeking a highly motivated Research Associate for a contract-based role to support the successful execution of a clinical study on-site at CMC Ranipet. This position, with a contract duration of 6+ months, involves working directly with the study team to ensure that the clinical trial is conducted in full compliance with the study protocol and regulatory standards. The Research Associate will assist in various aspects of the study, including patient management and data collection, and will report to the Clinical Research Associate. Flexibility in working both day and night shifts is essential to meet study requirements. Key Responsibilities:
  • Study Execution: Assist in conducting the clinical study in accordance with the protocol, ensuring compliance with all applicable regulatory and ethical guidelines.
  • Patient Management: Support the recruitment, screening, and enrollment of study participants. Guide participants through the informed consent process and ensure clear communication of study procedures.
  • Data Collection: Collect accurate and timely clinical data from participants, ensuring all information is properly documented in study records. Conduct source data verification to ensure consistency and accuracy.
  • Shift Coverage: Work both day and night shifts to oversee study activities and ensure continuous monitoring and data collection as per study protocol.
  • Protocol Adherence: Ensure that study procedures are conducted as per Good Clinical Practice (GCP) guidelines and the study protocol. Monitor patient care and assist with troubleshooting study-related issues as needed.
  • Regulatory Compliance: Assist in maintaining study documentation, ensuring that all files are up to date and meet regulatory and sponsor requirements.
  • Communication: Act as a key point of contact between the investigators, study participants, and the research team. Ensure clear and timely communication of study updates, issues, and results.
  • Supervision: Report directly to the Clinical Research Associate, providing updates and ensuring smooth study operations.
Requirements:
  • Bachelor's degree in life sciences, biomedical engineering, biotechnology, health sciences, pharmacy, or a related field.
  • Experience: 0-1 year of experience in clinical or academic research (fresh graduates with relevant qualifications are encouraged to apply).
  • Ability to work independently and manage multiple tasks with a high level of detail and accuracy.
  • Ability to work in a team, demonstrating strong collaboration and communication skills with study staff, investigators, and participants.
  • Willingness to work flexible hours, including day and night shifts, to support continuous study operations.
Preferred Skills:
  • Previous experience in a clinical or hospital research environment.
  • Basic understanding of clinical trial processes, GCP guidelines, and study monitoring.
  • Strong organizational skills and attention to detail, with the ability to ensure compliance with protocols and regulatory requirements.

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