Marcantonio Lab Clinical Research Coordinator

Beth Israel Lahey Health • Boston, MA

1d • $19 - $28 • Onsite

About The Position

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results. Works closely with other clinical research staff. The Marcantonio lab group is interested in hiring a full time Clinical Research Coordinator (CRC) for work primarily on a delirium (changes in memory and thinking during hospitalization) study (READI-SET-GO). The role includes patient screening, recruitment, and assessment for delirium. The CRC will also be responsible for reviewing medical records, following-up with patients and family members, and assisting in study related areas as needed. Duties outside the study include maintenance of NIDUS delirium network research repositories, and assisting with existing biorepository. This is an on-site position at Beth Israel Deaconess Medical Center, Boston. This position would be ideal for a recent graduate looking for 2-3 year experience in both the clinical and research spheres of medicine. Predecessors of the position have matriculated to medical school and PhD programs.

Requirements

• Bachelor's degree required.
• 0-1 year of related work experience required.
• Medical terminology.
• Working knowledge of computer systems required, including web-based applications and some Microsoft Office applications, which may include Outlook, Word, Excel, PowerPoint or Access.

Responsibilities

• Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol.
• Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal investigator.
• 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.
• 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 principal investigator and/or research nurse. Begins to learn how to independently resolve problems with protocol.
• 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.
• Assists clinic staff in obtaining insurance approval for subject protocol participation and scheduling tests and arranging admissions or outpatient visits for subjects.
• Assists investigator with correspondence with IRB.
• As needed, may function in areas/clinics performing job duties related to clinical research studies.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level