Clinical Research Associate (CRA) – Ahmedabad, India
Company: Veeda Clinical Research
Location: Ahmedabad, India
Employment Type: Full-Time, Permanent
Experience Required: 1–3 Years
Salary: ₹2.5–4 LPA
Openings: 2
Role Overview
Veeda Clinical Research is seeking a Clinical Research Associate (CRA) with 1–3 years of experience to support clinical trial monitoring and operations. The CRA will play a pivotal role in off-site monitoring, site management, regulatory compliance, and documentation across various phases of clinical trials.
This position offers exposure to site initiation, monitoring, and close-out activities while ensuring adherence to GCP, ICH guidelines, and study protocols. The role is ideal for professionals with a background in pharmacy, life sciences, or clinical research who are seeking to advance their career in clinical operations.
Key Responsibilities
Off-Site Monitoring
Conduct off-site monitoring visits across study phases as per the study plan
Perform initial site visits to train and guide site personnel, ensuring site readiness per protocol requirements
Execute routine monitoring visits at predefined intervals to ensure compliance with study guidelines
Communication & Documentation
Engage with potential study sites for feasibility assessments and gather required data for review
Follow up with off-site personnel and prepare standardized monitoring and site visit reports (Pre-study Qualification Report, Site Initiation Visit Report, Site Monitoring Visit Report, Site Closeout Visit Report)
Collect essential study documents (calibration reports, agreements, and regulatory documents) from sites and vendors
Maintain accurate study logs, forms, source data templates, recruitment trackers, and feasibility questionnaires
Audits & Compliance
Review study-related documents to ensure adherence to SOPs, ICH-GCP guidelines, and regulatory requirements
Train, guide, and mentor off-site teams on protocol compliance and updated regulatory requirements
Respond to internal and external audit queries from QA/QC teams, sponsors, and regulatory authorities
Perform additional tasks assigned by the reporting authority to support clinical trial delivery
Required Qualifications & Skills
Postgraduate degree: M.Pharm (any specialization) or M.Sc / MS in Life Sciences or related field
Experience: 1–3 years in clinical trial monitoring, clinical operations, or clinical research
Knowledge of ICH-GCP, clinical trial protocols, site monitoring, and clinical data management
Strong organizational, communication, and analytical skills
Proficiency in preparing site visit reports, feasibility questionnaires, and clinical documentation
Ability to work collaboratively with cross-functional teams and vendors
Preferred Skills
Site initiation and monitoring experience
Clinical trial execution and site management expertise
Exposure to clinical data management systems
About Veeda Clinical Research
Veeda CR is a leading clinical research organization (CRO) providing end-to-end clinical trial services to the pharmaceutical and biotechnology industries. With a focus on quality, compliance, and patient-centric approaches, Veeda supports global sponsors in delivering high-quality clinical trial outcomes.
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