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Clinical Research Associate

2-5 Years
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  • Posted 6 days ago
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Job Description

  • Ensure clinical research studies are conducted in compliance with protocol, SOPs, Good Clinical Practice (GCP) guidelines, and other regulatory requirements.
  • Perform site selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work and GCP guidelines.
  • Review and oversee informed consent documents and procedures.
  • Negotiate study budgets with investigators and assist in execution of site contracts.
  • Provide site management and monitoring visits for multiple protocols and sites.
  • Train site personnel on protocol and study-related procedures, and establish regular communication to manage project expectations.
  • Evaluate the quality and integrity of study site practices, ensuring adherence to protocol and regulations.
  • Escalate quality issues to Clinical Project Manager or line manager when necessary.
  • Ensure accurate data reporting through review of site source documents and medical records.
  • Identify protocol deviations and assess risks to subject safety and data integrity.
  • Perform investigational product accountability as per protocol and Study Monitoring Plan.

More Info

Job Type:
Employment Type:
Open to candidates from:
Indian

About Company

Seven Consultancy is a result of the motivation of young entrepreneurship under the guidance of experienced professional from industry. Young entrepreneurs know the recent trends of market. Flexibility of the services has helped Seven consultancy to secure a brand name in the market. So we have access to an overall career solution. Seven consultancy believes in shaping the way of success for its clients. Journey of Seven Consultancy started in 2007. Now it has crossed many milestones and added so many feathers in its crown. Currently operating from Kolkata & Mumbai to provide services all over India & abroad.

Job ID: 135565567

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