Vacancy expired!
Actalent is looking for a tenured Clinical Research Coordinator to join our team! Description : Our client is seeking a CRC to work with a research group helping support clinical trials with on of the largest healthcare providers in the nation. This is a great opportunity for anyone interested in working in the Medical Center Responsibilities : All phases of clinical trials including pre-study implementation to study closure.
Discuss clinical trials with eligible patients.
Patient screening, review eligibility for clinical trial to protocol.
Scheduling protocol study visits and patient follow up.
Must have experience conducting the full life cycle of a clinical trial.
Qualifications : Must have at least 2-4+ years as a clinical research coordinator.
Must have experience working on Neurology and/or Stroke trials.
Must be flexible to work on multiple studies.
Must have experience drawing own labs.
Experience working in high enrolling studies in a plus.
Additional Information:Schedule: 8:00 am - 5:00 pm.
They must be flexible to come in early or stay late depending on the needs of the patient.
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
