Clinical Research Associate (CRA)

Kolkata, India | Clinical Operations | 2-4 years

We are seeking a highly motivated and experienced Clinical Research Associate to join our growing Clinical Operations team in Kolkata. This role is crucial for ensuring the successful execution and monitoring of clinical trials, adhering to ICH-GCP guidelines and regulatory requirements.

Key Responsibilities:

• Conducting site selection, initiation, monitoring, and close-out visits.
• Ensuring compliance with study protocols, SOPs, and regulatory guidelines.
• Verifying source data, reviewing CRFs, and resolving data queries.
• Managing site performance, patient recruitment, and retention.
• Providing ongoing training and support to investigative site staff.
• Preparing and submitting site visit reports and follow-up letters.

Qualifications:

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field.
• 2-4 years of independent clinical monitoring experience in a CRO or pharmaceutical company.
• Thorough knowledge of ICH-GCP guidelines and relevant local regulations.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel extensively as required.

What We Offer:

• Competitive salary and performance bonuses.
• Comprehensive health and wellness benefits.
• Opportunities for professional development and training.
• Dynamic and collaborative work environment.
• Contribution to impactful medical research.