Medical Assistant - Clinical Research (Overnight Shift)

About Us

• Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials.
• Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country.
• Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
• Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.
• We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Hourly Rate

$20.00/hr (depending on education, experience, and skillset) + 4hours of OT each day

Schedule

• Full-Time 3X12 shifts 6:00
• PM - 6:00 AM (Weekend Availably)

Job Summary

Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.

Essential Responsibilities and Duties

• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.