Company: Veeda Clinical Research Limited
Location: Ahmedabad, India
Position: Protocol Writer
Experience: 3-4 Years
Qualification: B.Pharm / M.Pharm / Pharm D
Veeda Clinical Research Limited is a premier Contract Research Organization (CRO) specializing in clinical trial management and drug development services. We are dedicated to delivering high-quality solutions that adhere to global regulatory standards and drive advancements in healthcare.
As a Protocol Writer at Veeda Clinical Research Limited, you will be responsible for developing and reviewing clinical trial protocols. You will collaborate closely with cross-functional teams to ensure protocols are comprehensive, scientifically sound, and aligned with regulatory guidelines and sponsor requirements.
Protocol Development:
Protocol Review and Approval:
Scientific and Regulatory Compliance:
Cross-functional Collaboration:
Documentation and Reporting:
Quality Assurance and Improvement:
Educational Background:
Experience:
Technical Skills:
Communication and Collaboration:
Attention to Detail:
Interested candidates who meet the qualifications are encouraged to submit their resume and cover letter to careers@veedacr.com with the subject line "Application for Protocol Writer - Ahmedabad."
Join Veeda Clinical Research Limited and contribute to shaping the future of clinical trials through impactful protocol development and adherence to global regulatory standards.
Note: This job description serves as a general overview and may include additional responsibilities and qualifications as required by Veeda Clinical Research Limited.
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