
Clinical Research Coordinator
1 day ago
We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team. As a key member of our research department, you will be responsible for facilitating and coordinating daily clinical study activities.
Main Responsibilities:
- Recruit and coordinate research participants and ensure their needs are met.
- Review and develop a thorough understanding of the protocol, including study proceedings, timelines, inclusion and exclusion criteria, and confidentiality requirements.
- Attend investigator meetings as required or requested by the Principal Investigator (PI).
- Translate study documents as needed.
- Serve as liaison with the Ethics Review Committee (ERC), preparing and submitting study documents, such as progress reports.
- Prepare other study materials, including informed consent documents, case report forms (CRFs), and data collection tools.
- Establish and organize study files, including regulatory binders, source documentation, and other materials.
- Assist in preparing all documents related to the informed consent process.
- Conduct the informed consent process with research participants, addressing questions and obtaining necessary signatures and dates.
- Screen subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's status.
- Coordinate participant tests and procedures.
- Collect data as required by the protocol, ensuring timely completion of CRFs.
- Maintain adequate inventory of study supplies, as deemed necessary.
- Complete study documentation and maintain study files according to ERC requirements and policies.
- Foster effective communication with research participants and the PI throughout the study.
- Collaborate with the PI to manage day-to-day study activities, including problem-solving, communication, and protocol management.
- Manage study data and complete data entry accurately.
- Participate in qualitative research, involving coordination of interviews and focus groups, conducting interviews, facilitating and observing focus groups, transcribing audio data, and contributing to data analysis.
- Perform additional tasks as requested by the Head of Unit.
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