Research Coordinator Jobs

About The Position

Requirements

• Bachelor’s degree in Health Science or Science.

Responsibilities

• Work in collaboration with the Principal Investigator (PI).
• Assist the Regulatory Specialist with maintaining and retaining regulatory documents in accordance with sponsor requirements.
• Conduct protocol and feasibility evaluations.
• Assess patient populations and recruitment and enrollment strategies.
• Recruit and manage trial subjects, including screening for protocol eligibility, covering informed consent, and applying screening and inclusion/exclusion criteria while adhering to safety and compliance requirements.
• Assist with accurate and timely data collection, source-document documentation, data entry, and reporting.
• Schedule, coordinate, plan, and participate in monitoring and auditing activities.
• Participate in required training and education programs.
• Assist the PI in developing materials and tools to train study personnel on protocol requirements, subject-visit schedules, and research-plan execution.
• Maintain documentation of training.
• Maintain effective and timely communications with the sponsor, research subjects, and PI throughout the study.
• Provide a safe environment for patients, families, and clinical staff by complying with federal, state, and professional regulatory standards.
• Report instances of noncompliance to the appropriate institutional oversight body.
• Maintain strict patient confidentiality in accordance with HIPAA regulations and applicable law.
• Follow clinical procedures and guidelines established by regulatory bodies.
• Support clinical-trial close-out, including contributing to research articles, audit preparation, trial closure, communications with authorities and involved disciplines, assistance with the final study report, completion of financial obligations, and archiving study materials.

Benefits

• Comprehensive benefits package for team members and providers.