Nucleon Research Pvt. Ltd. is hiring for the position of Clinical Research Associate (CRA) in Thane, Maharashtra. Candidates with a minimum of one year of on-site clinical monitoring experience can apply for this clinical research opportunity.

The role involves clinical trial site monitoring, regulatory compliance, source document review, protocol deviation management, and coordination with investigators and clinical research teams.

Nucleon Research Recruitment – Job Details

Position: Clinical Research Associate

The Clinical Research Associate will conduct clinical trial monitoring activities and ensure that trial sites follow approved protocols, ICH-GCP guidelines, standard operating procedures (SOPs), and applicable regulations.

Roles and Responsibilities

• Conduct site initiation, routine monitoring, and close-out visits.
• Ensure compliance with clinical trial protocols, ICH-GCP, SOPs, and regulations.
• Review source documents, Case Report Forms (CRFs), and other clinical trial documentation.
• Support site management and query resolution.
• Identify, document, and follow up on protocol deviations and compliance issues.
• Maintain accurate monitoring reports and trial documentation.
• Coordinate with investigators, site staff, and project teams.

Eligibility Criteria

• Minimum one year of on-site clinical monitoring experience.

Key Skills and Responsibilities

• Clinical trial site monitoring.
• ICH-GCP and regulatory compliance.
• Source document and CRF review.
• Protocol deviation identification and follow-up.
• Clinical trial documentation and monitoring reports.
• Site coordination and query resolution.

How to Apply

Interested candidates can send their CV to the recruitment contact provided below.

• Email: prashant.sabane@nucleonresearch.com
• Company: Nucleon Research Pvt. Ltd.