If you’re a passionate professional looking for a career in clinical research, Veeda Clinical Research Limited has an exciting opportunity for you! This rapidly growing Contract Research Organization (CRO) is looking for talented Clinical Research Associates (CRAs) to join its dynamic team in Ahmedabad.

Company Introduction

Veeda Clinical Research Limited is a leading independent CRO providing comprehensive clinical research and development solutions to the global biopharmaceutical industry. Known for its commitment to innovation, quality, and regulatory compliance, Veeda ensures the successful execution of clinical trials while adhering to the highest standards of ethics and scientific integrity.

Job Title: Clinical Research Associate (CRA)

Location: Ahmedabad
Experience: 1-3 years

Qualification

To apply for this role, candidates must have one of the following qualifications:

• MPharm
• BPharm
• PharmD
• MSc in Life Sciences or related fields

Key Responsibilities

Off-site Monitoring

1. Conduct off-site visits during various study phases, including initial site visits to train and guide site personnel.
2. Inspect site readiness by evaluating pre-requisites as per study protocols.
3. Undertake routine monitoring visits at predetermined intervals as per study guidelines.

Communication & Documentation

1. Manage Feasibility Assessment Questionnaires (FAQ) and collect necessary information from potential sites for review.
2. Perform regular follow-ups with off-site nodal/in-charge personnel and prepare comprehensive visit reports such as:
   • Pre-study Qualification Report
   • Site Initiation Visit Report
   • Site Monitoring Visit Report
   • Site Closeout Visit Report
3. Submit timely and accurate reports to update on study trial progress.

Audits & Compliance

1. Review study-related documents to ensure adherence to Standard Operating Procedures (SOPs), protocols, and regulatory requirements.
2. Train, guide, and mentor off-site teams on study protocols, Good Clinical Practice (GCP), Root Cause Analysis, and updated regulatory requirements.
3. Respond to and comply with queries raised during internal (QA/QC) and external (Sponsor/Regulatory) audits.

Skills Required

• Strong understanding of clinical trial processes and GCP guidelines.
• Excellent communication and organizational skills.
• Attention to detail for accurate reporting and documentation.
• Ability to train and mentor team members.
• Proficiency in using clinical research tools and software.

How to Apply

Interested candidates can apply by sharing their updated resumes to Vaibhav.D3662@veedacr.com. While submitting your application, ensure you mention the position “Clinical Research Associate (CRA)” in the subject line.

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