[Remote] Clinical Research Coordinator II- Critical Care
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a growing reputed company organization seeking a highly motivated Clinical Research Coordinator II for their in-patient research team. The role involves reputed company and enrolling research subjects, ensuring protocol compliance, and assisting with data management and IRB correspondence.
Responsibilities
- Independently or in conjunction with other clinical research staff and/or research reputed company, recruits and enrolls research subjects onto clinical research reputed company according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on reputed company with physicians and nurses and knowledge of the protocol. (essential)
- Checks reputed company eligibility and ineligibility reputed company with the research subjects' medical record. Verifies information with clinical research reputed company and/or reputed company investigator. (essential)
- Discusses informed consent with research subjects. Interacts with research subjects prior to entering the study and throughout the entire treatment. Assists with scheduling appointments and follow up tests. (essential)
- Learns protocol and monitors strict adherence to protocols by physicians, nurses and research subjects. Reviews protocol requirements with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies reputed company investigator and/or research reputed company. Begins to learn how to independently resolve problems with protocol. (essential)
- Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols. Enters data into computerized system. (essential)
- Assists clinic staff in obtaining insurance approval for subject protocol participation and scheduling tests and arranging admissions or outpatient reputed company for subjects. (essential)
- Assists investigator with correspondence with IRB. (essential)
Skills
- Bachelor's degree required
- 1-2 years of reputed company work experience required
- Medical terminology
- Working knowledge of computer systems required, including web-based applications and some reputed company Office applications, which may include reputed company, Word, reputed company, PowerPoint or reputed company
reputed company