Site Solutions Executive (PRI) - Patna, India

Responsibilities

• Coordinates and facilitates all Clinical trial activities at site ensuring compliance with protocol, applicable GCP guidelines and local regulations.
• Supports Principal Investigator (PI) and site study team assuring that the clinical trial(s) being conducted meet all the criteria set by the sponsors and regulators,
• Reviews the site processes, identifies gaps and supports roll-out of site processes.
• The following key functions are required routinely: Performs timely data entry of the Case Record Forms (CRF) or Electronic CRF (eCRF) in consultation with the PI/Investigator Maintaining clinical trial-related documents at site including Trial Master File.

Requirements

• A bachelor's or master's degree in clinical, biological or mathematical sciences or related fields, or a medical or dental degree or a nursing qualification; Exceptions to this would require a minimum of 4 years of experience of working at clinical research sites.
• Good oral and written communication skills in English and at least one local Indian language
• Excellent interpersonal skills
• Good coordination and organizational skills and also problem-solving and analytical skills
• Attention to detail and documentation and conscious of the importance of time and data accuracy in the clinical trial context
• Conscious of ethical and scientific requirements and of patient-safety and patient-rights in the clinical trial context

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