Clinical Research Coordinator

A Clinical Research Coordinator (CRC) is a specialized role in healthcare research, overseeing the day-to-day management of clinical trials. They work closely with principal investigators and other research team members to ensure that studies are conducted safely and by strict regulatory guidelines. 

While traditionally done in hospitals or clinics, this role can also function remotely by using digital tools to monitor patient data, communicate with study participants, and manage documentation from a distance.

CRCs manage the logistics of clinical studies, from recruiting and enrolling participants to tracking their progress and handling data. They are responsible for ensuring patient safety, organizing study materials, and ensuring data accuracy and integrity. 

Remotely, CRCs use secure online systems to handle records, monitor patient health through telemedicine platforms, and maintain constant communication with both participants and the rest of the research team. This setup enables clinical research to proceed efficiently even without an on-site presence.

Are you ready to lead groundbreaking clinical research that impacts patient care? 

Join our team as a Clinical Research Coordinator (CRC) and be at the heart of our clinical studies!

In this pivotal role, you’ll oversee and coordinate all aspects of clinical trials, from patient recruitment to data collection, ensuring the highest safety and compliance standards. 

As the linchpin of our research operations, you'll establish protocols, manage study timelines, and oversee participant interactions, making critical decisions that drive the success of each study. 

Collaborating with cross-functional teams, you'll track progress, ensure accurate data, and champion best practices, fostering an environment of excellence in clinical research!

• Coordinate clinical research studies from initiation to closure
• Recruit and screen potential study participants
• Obtain informed consent from participants and maintain proper documentation
• Collect and manage research data accurately
• Assist in the preparation and submission of regulatory documents
• Schedule study visits and manage study-related procedures
• Communicate with study sponsors, investigators, and study participants
• Ensure adherence to study protocols and compliance with regulations
• Monitor participant safety and report adverse events as necessary
• Participate in study meetings and trainings
• Collaborate with multidisciplinary teams to ensure study success
• Maintain study files and records in an organized manner
• Assist in the development of study protocols and procedures
• Conduct quality control checks to ensure data integrity
• Follow Good Clinical Practice (GCP) guidelines and company SOPs

• Achieved recruitment targets for clinical research studies.
• Ensured regulatory compliance throughout the study duration.
• Maintained data confidentiality and integrity throughout the study.
• Met study milestones and timelines effectively.
• Provided timely and accurate reports on study progress.
• Facilitated smooth study operations and participant management.
• Ensured all study documentation was complete and accurate.

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• Bachelor's degree in a related field (such as health sciences or life sciences)
• Previous experience in clinical research coordination or a related role
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
• Strong organizational and time management skills
• Excellent communication and interpersonal abilities
• Attention to detail and accuracy in data management
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office suite and research database systems
• Certification in clinical research is a plus
• Commitment to upholding ethical standards in research conduct