Clinical Research Associate

Job Description

·       Protocol Review: Review and understand the study protocol, which outlines the objectives, design, methodology, and conduct of the clinical trial.

·       Site Selection: Participate in the selection of appropriate clinical trial sites and investigators based on their qualifications and ability to conduct the study.

·       Regulatory Compliance: Ensure that the clinical trial is conducted incompliance with relevant regulatory requirements, including Good Clinical Practice (GCP) guidelines. Assist in the preparation for and conduct of regulatory inspections.

·       Site Initiation: Conduct site initiation visits to train investigators and site staff on the protocol, regulatory requirements, and data collection procedures.

·       Monitoring: Regularly visit clinical trial sites to monitor the conduct of the study, including the verification of data accuracy, participant safety, and protocol adherence.

·       Data Collection and Management: Oversee the collection, documentation, and verification of clinical trial data, ensuring that it is accurate, complete, and in compliance with the protocol.

·       Safety Reporting: Monitor and report adverse events, protocol deviations, and other safety-related issues in accordance with regulatory requirements.

·       Communication: Maintain regular communication with investigators, site staff, and study sponsors to address queries, provide guidance, and ensure the smooth progress of the trial.

·       Documentation: Maintain and review essential documents, such as informed consent forms, ethics committee approvals, and other regulatory documents, to ensure compliance.

·       Close-Out Visits: Conduct close-out visits to ensure that all required documentation is complete, and study materials are returned, and provide support for the finalization of the study report.

·       Quality Assurance: Collaborate with quality assurance teams to ensure that the clinical trial processes adhere to quality standards and are audit-ready.

·       Training: Provide training and support to site personnel on an ongoing basis to maintain protocol adherence and data integrity.

Job Requirements

·       Education: A bachelor's degree in a relevant scientific or healthcare field. Degree in pharmacy, nursing, or MBBS preferred.

·       Clinical Research Certification: Certified Clinical Research Professional (CCRP) or the Society of Clinical Research Associates (SoCRA) certification is a plus.

·       Experience: Minimum 2 years of clinical monitoring experience in oncology trials.

·       Knowledge of Regulations and Guidelines: A good understanding of Good Clinical Practice (GCP)guidelines, relevant regulatory requirements (such as FDA regulations), and other guidelines governing clinical research.

·       Attention to Detail: Strong attention to detail to ensure accuracy in data collection and compliance with protocols.

·       Communication Skills: Effective communication with study site personnel, investigators, and sponsors. Able to convey complex information clearly and professionally.

·       Organizational Skills: Strong organizational skills to keep track of various aspects of the clinical trial.

·       Problem-Solving Skills: The ability to identify and resolve issues or challenges that may arise during the course of a clinical.

·       Teamwork: Ability to collaborate effectively with various stakeholders, including investigators, study coordinators, and sponsors.

·       Ethical Conduct: Posses high ethical standards to ensure the safety and well-being of study participants and the integrity of the clinical trial data.

·       Computer Skills: Proficiency in using various computer applications and clinical trial management systems.

·       Travel Availability: Willingness and ability to travel to different clinical trial sites.

·       Adaptability: Able to adapt to changes in study protocols, regulations, or project requirements.