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).
Responsibilities- Collects and records study data. Inputs all information into database.
- Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
- Screens patients for eligibility through medical record review and upcoming visit in the RI.
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls screening participants for eligibility registering subjects with sponsoring agency administering lifestyle questionnaires.
- Assists in preparing grant applications IRB/GCO for submission and filings.
- Assists with data analysis as needed.
- Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
- Secures delivers and ships clinical specimens as required by the protocol.
- Prepares data for management meetings.
- Performs other related duties.
- Manages Study Data of Ongoing Clinical research projects Under Supervision of the Principal Investigator(s).
- Ensure Proper Compliance with Institutional and Regulatory Requirements.
- Attends weekly ILD meeting.
- Assists the Principal Investigator(s) and regulatory staff in the preparation of new protocol submissions protocol amendments and renewals of ongoing clinical projects.
- Working knowledge of Good Clinical Practice guidelines and Federal Research regulations.
- Strong organizational and communications skills.
- Comfort with communicating clinical information to medical personnel.
- Ability to work on a team and individually.
- Ability to identify analyze and solve problems while working under pressure.
- Strong computer literacy.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience
Required Experience:
IC