Veeda Clinical Research HirQuality Control Professional for Clinical Trials in Ahmedabad

Veeda Clinical Research Ltd, a leading name in the industry, is on the lookout for talented individuals to join their team. We are currently hiring for the position of Quality Control – Clinical Trials in Ahmedabad. If you have a background in QA/QC with 3 to 5 years of experience, we encourage you to explore this exciting opportunity.

Vacancies List:

• Quality Control – Clinical Trials

Company Name:

Veeda Clinical Research Ltd

Salary: Competitive

Company Address: Ahmedabad

Detailed Job Description:

As a Quality Control professional specializing in Clinical Trials, your role is pivotal in ensuring the quality and regulatory compliance of deliverables in this critical domain. Your responsibilities will include:

Role:

• Preparation, review, and coordination of SOPs, ensuring timely revisions.
• Preparation and support of sponsor and regulatory inspections.
• Review of Instrument Calibration/Qualification documents.
• Review of software validation documents and liaising with vendors for software improvement/validation/tracking.
• Ensuring compliance with applicable cross-functional SOPs.
• Facilitating system audits and closing observations.
• Tracking, managing, and following up on timely closing of deviations, CCF, CAPA, and incidence reports.
• Ensuring compliance with folder management activities.
• Archival of COD-related documents.
• Maintenance and handling of common department-related files.

Project-Specific Responsibilities:

• Plan, prepare, conduct, and monitor various QC activities to ensure compliance.
• Review study protocol, ICF, regulatory documents, and other study-related documents.
• Review trial master files and clinical investigator files.
• Support monitoring for monitoring visits as required.
• Provide support and guidance to the clinical operation team for day-to-day trial-related activities.
• Periodic review/tracking of the status of various reports and audit responses.
• Periodic review of Protocol deviations and other identified critical activities.
• Any other responsibilities assigned by HOD/designee.

Experience:

• Must be a postgraduate (MSc., M.Pharm, or equivalent).
• Minimum of 3 years of experience in QA/QC roles.

How to Apply:

Interested candidates meeting the qualifications are invited to send their resumes to dhonisha.s2315@veedacr.com. Join us in ensuring quality and compliance in Clinical Trials.