Clinical Trial Assistant (CTA) / Clinical Research Associate (CRA)

VHypotenuse Private Limited

Website: vhypotenuse.com
Job details:

Location: Arunachal Pradesh, India (Local candidates only)

Experience: 1–3 years

Job Summary:

We are seeking a highly motivated and detail-oriented Clinical Trial Assistant (CTA) / Clinical Research Associate (CRA) to support clinical trial activities in Arunachal Pradesh. The ideal candidate should have 1–3 years of relevant clinical research experience and must be currently residing in Arunachal Pradesh to effectively manage site-level activities and coordination.

Key Responsibilities:

• Assist in the planning, initiation, monitoring, and close-out of clinical trials in compliance with applicable regulatory guidelines.
• Support site management activities including site identification, feasibility, and initiation visits.
• Ensure accurate and timely documentation, including maintenance of Trial Master File (TMF) and regulatory documents.
• Coordinate with investigators, site staff, and cross-functional teams for smooth trial execution.
• Monitor site performance, patient recruitment, and data quality.
• Conduct on-site and remote monitoring visits as required.
• Ensure adherence to protocol, GCP (Good Clinical Practice), and SOPs.
• Assist in resolving site-related issues and queries.
• Support audit and inspection readiness activities.

Qualifications & Requirements:

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.
• 1–3 years of experience in clinical research (CTA/CRA role preferred).
• Strong understanding of ICH-GCP guidelines and clinical trial processes.
• Excellent communication and organizational skills.
• Ability to work independently and manage multiple tasks effectively.

Mandatory Requirement:

• Candidates must be currently residing in Arunachal Pradesh.
• Preference will be given to candidates with local site experience and familiarity with the region.

Preferred Skills:

• Experience in site monitoring and management.
• Familiarity with regulatory requirements in India.
• Proficiency in MS Office and clinical trial systems.

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