Clinical Research Coordinator

Study CoordinationManages the day-to-day activities of clinical trials.Ensures compliance with study protocols and regulatory requirements.Coordinates participant recruitment, screening, and enrollment.Maintains accurate and timely documentation of study activities.Data ManagementCollects, enters, and verifies clinical trial data.Ensures data integrity and accuracy.Prepares data reports for review by the PI and sponsors.Manages electronic data capture systems.Regulatory CompliancePrepares and submits regulatory documents to IRBs and other regulatory bodies.Ensure ethical approval for studies is maintained, from initial approval through amendments, annual renewals, and terminations.Ensures adherence to Good Clinical Practice (GCP) guidelines.Maintains regulatory binders and essential documents.Coordinates audits and inspections.Informs and consents study participants.Schedules and conduct study visits.Monitors participant safety and well-being.Provides education and support to participants.Collaboration and CommunicationCommunicates study progress and issues to the PI and research team.Liaises with sponsors, monitors, and other external stakeholders.Participates in team meetings and training sessions.Facilitates effective teamwork and collaboration.Marginal or Periodic Functions:Assists with grant writing and funding applications.Participates in the development of study protocols and procedures.Attend professional development workshops and conferences.Provides mentorship and training to junior research staff.Adheres to internal controls and reporting structure.Performs related duties as required.Participant InteractionInforms and consents study participants.Schedules and conduct study visits.Monitors participant safety and well-being.Provides education and support to participants.Collaboration and CommunicationCommunicates study progress and issues to the PI and research team.Liaises with sponsors, monitors, and other external stakeholders.Participates in team meetings and training sessions.Facilitates effective teamwork and collaboration.KNOWLEDGE/SKILLS/ABILITIESEnsures accuracy in data collection and documentation.Identifies and corrects errors promptly.Maintains meticulous records.Clearly conveys information to participants and team members.Facilitates effective collaboration.Provides clear and concise reports.Manages multiple tasks and priorities efficiently.Maintains organized study files and documentation.Ensures timely completion of study activities.Identifies and resolves issues that arise during studies.Develop solutions to improve study processes.Thinks critically and analytically.Utilizes electronic data capture systems effectively.Understands medical terminology and clinical research methods.Adapts to new technologies and software.