Clinical Research Coordinator in Clacton-on-Sea

The Clinical Research Coordinator is a member of the study team who, under the direction of the Principal Investigator and Director of Research Operations, is responsible for the overall coordination of assigned minimal‐risk studies, including regulatory submissions, screening, recruitment, data collection, and data entry to ensure protocol compliance and human subjects protection.

Key Accountabilities

• Serve as the primary coordinator on minimal‐risk studies.
• Serve as liaison between study team, research cores/units/departments, ancillary hospital departments/services, sponsor, and IRB to ensure cross‐communication and protocol compliance.
• Coordinate the preparation and submission of regulatory documentation to the sponsor and Institutional Review Board (IRB) during all phases of study conduct, including start‐up, continuing reviews, changes in research, problem events, and closure, to ensure human subjects' protection and regulatory compliance.
• Operationalize the recruitment plan and obtain or coordinate the informed consent process to ensure the participant understands the information and volunteers to participate free of coercion.
• Coordinate and/or perform study visits/interventions/observations to ensure they are conducted according to protocol.
• Monitor participants for adverse events and study conduct for protocol deviations and events and report accordingly to the Principal Investigator, sponsor, and IRB to ensure participant safety and protocol compliance, and participate in the Corrective and Preventive Action planning where applicable.
• Coordinate and perform data collection from various sources, including medical records, and enter data into the research database to ensure accurate and timely data entry.
• Maintain organized and up‐to‐date research records, including regulatory binders and participant records, to ensure study documentation is audit‐ready.

Qualifications

• Bachelor's degree in science or a health‐related field.
• 2 years of prior clinical research assistant, direct patient care services, or nursing or other healthcare‐related certification experience.
• Computer competency in using Microsoft Office, including Word, Excel, and Outlook.
• Ability to follow protocols and directions very closely.
• Ability to read, write, and speak English, and be comfortable communicating with patient populations.
• Prior experience utilizing Electronic Medical Records (EMR).
• Ability to travel throughout the JHACH service areas in a timely manner.

Salary Range: Minimum 25.32/hour - Maximum 40.52/hour. Compensation will be commensurate with equity and experience for roles of similar scope and responsibility.

The Hospital reserves the right to modify employee schedules as needed. We are committed to creating a welcoming and inclusive environment, where we embrace and celebrate our differences, where all employees feel valued, contribute to our mission of serving the community, and engage in equitable healthcare delivery and workforce practices.

Johns Hopkins Health System and its affiliates are an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, mental or physical disability, genetic information, veteran status, or any other status protected by federal, state, or local law.

Johns Hopkins Health System and its affiliates are drug‐free workplace employers.