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Trialcraft Clinical Research Hiring For Quality Clinical Research Executive

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Trialcraft Clinical Research

B.Pharm, M.Pharm, Msc, BSc, Lifesciences

Kanchipuram, Tamil Nadu, India

1 - 2 Years

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Trialcraft Clinical Research Services Pvt. Ltd is a leading name in the clinical research industry, specializing in end-to-end clinical trial management. The company excels in site management, monitoring, and execution of Phase II, III, and IV clinical trials for pharmaceutical, biological, and medical device products. With a strong focus on global clinical trials, Trialcraft identifies target patient populations accurately and implements cost-effective strategies to ensure timely enrollment and successful trial completion.


Job Description: QA Executive – Clinical Research

Trialcraft Clinical Research Services Pvt. Ltd is seeking a dedicated and detail-oriented QA Executive to join their team in Kanchipuram. This is a full-time, on-site role where you will play a critical part in ensuring the quality and compliance of clinical research projects.

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Key Responsibilities:

  • Conduct quality control and quality assurance activities for clinical research projects.
  • Implement and manage quality management systems to ensure compliance with regulatory standards.
  • Perform quality audits to identify areas for improvement and ensure adherence to protocols.
  • Maintain a strong understanding of FDA regulations and Good Clinical Practice (GCP) guidelines.
  • Collaborate with cross-functional teams to resolve quality-related issues and ensure project timelines are met.
  • Prepare and maintain detailed documentation for audits, inspections, and quality reports.
  • Stay updated with industry trends and regulatory changes to ensure continuous improvement in quality processes.

Qualifications:

  • Bachelor’s degree in Pharmacy, Life Sciences, or a related field.
  • 1-2 years of experience in quality assurance, preferably in the clinical research or pharmaceutical industry.
  • Strong knowledge of quality control, quality management, and quality auditing processes.
  • Familiarity with FDA regulations and GCP guidelines.
  • Excellent attention to detail, analytical skills, and problem-solving abilities.
  • Effective communication and interpersonal skills to work collaboratively with teams.

Why Join Trialcraft?

  • Opportunity to work on global clinical trials and contribute to groundbreaking healthcare research.
  • Be part of a team that values innovation, quality, and compliance.
  • Gain hands-on experience in a dynamic and supportive work environment.

How to Apply:

If you are passionate about clinical research and meet the qualifications listed above, we encourage you to apply!

Email your resume to: hrtrialcraft@gmail.com

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