DescriptionThe Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).
We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a critical role in supporting two NIH-funded clinical research projects by focusing on patient recruitment participant engagement and coordination of study-related meetings. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators research staff and study participants
ResponsibilitiesPatient Recruitment & Enrollment
- Identify screen and recruit eligible patients into study protocols.
- Obtain informed consent in compliance with institutional and federal guidelines.
- Serve as a primary contact for participants ensuring a positive research experience.
- Study Coordination
- Schedule and coordinate study-related meetings including with investigators study staff and collaborators.
- Maintain accurate and timely study records logs and regulatory documentation.
- Assist with scheduling participant visits follow-up calls and reminders.
- Communication & Collaboration
- Act as a liaison between participants investigators and the research team.
- Coordinate with clinical and administrative staff to ensure smooth study operations.
- Provide regular updates to the principal investigators and project managers.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience
- Prior experience in clinical research patient recruitment or healthcare setting (preferred).
- Strong communication organizational and interpersonal skills.
- Ability to manage multiple priorities and work independently as well as part of a team.
- Familiarity with IRB processes research ethics and HIPAA compliance (preferred).
Required Experience:
IC
DescriptionThe Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Offi...
DescriptionThe Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).
We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a critical role in supporting two NIH-funded clinical research projects by focusing on patient recruitment participant engagement and coordination of study-related meetings. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators research staff and study participants
ResponsibilitiesPatient Recruitment & Enrollment
- Identify screen and recruit eligible patients into study protocols.
- Obtain informed consent in compliance with institutional and federal guidelines.
- Serve as a primary contact for participants ensuring a positive research experience.
- Study Coordination
- Schedule and coordinate study-related meetings including with investigators study staff and collaborators.
- Maintain accurate and timely study records logs and regulatory documentation.
- Assist with scheduling participant visits follow-up calls and reminders.
- Communication & Collaboration
- Act as a liaison between participants investigators and the research team.
- Coordinate with clinical and administrative staff to ensure smooth study operations.
- Provide regular updates to the principal investigators and project managers.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience
- Prior experience in clinical research patient recruitment or healthcare setting (preferred).
- Strong communication organizational and interpersonal skills.
- Ability to manage multiple priorities and work independently as well as part of a team.
- Familiarity with IRB processes research ethics and HIPAA compliance (preferred).
Required Experience:
IC
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