CLINICAL RESEARCH COORDINATOR A/ B

Location
Philadelphia
Posted
May 03, 2017
Administrative Jobs
Academic Affairs
Institution Type
Four-Year Institution

Duties: The clinical research coordinator A will provide staff support for clinical trials including data entry, organizing, maintaining and assuring the accuracy of all study documentation under the direction of his/her supervisor. The research coordinator A will be responsible for completing case report forms (CRFs), responding to queries in a timely manner, submission of AEs and SAEs to the sponsor and IRB per protocol. The clinical research coordinator A will provide support in the research clinic to screen patients, determine eligibility, consent and enroll patients. The research coordinator A will prepare a patient specific study calendar that outlines the steps (visits, procedures, labs etc.) required to participate in the trial.

The Clinical Research Coordinator B independently manages one or more clinical trials beginning with the study initiation visit (SIV) through study closeout.

The Research Coordinator B works closely with the faculty principal investigator (PI) in the day to day management of his/her research clinic to ensure the study compliance required for Good Clinical Practice. The Research Coordinator B will be responsible for supervising/training one or more Research Coordinator A and ensure that clinic nurses, nursing assistants and patient service representatives are fully oriented to the conduct of clinical trials.

Position is contingent on continued funding.

Qualifications: Clinical Research Coordinator A: Bachelor s Degree and 1 year to 2 years of experience or equivalent combination of education and experience is required. Proficiency in Excel, Word, Outlook, Internet and word processing/typing required. Requires the ability to handle confidential materials; prioritize and handle multiple assignments simultaneously; excellent communication and organizational skills and attention to detail. Ability to work independently, communicate effectively with patients, employees, study sponsor and their designees required.

Clinical Research Coordinator B: Bachelor s Degree and 2 years to 4 years of experience or equivalent combination of education and experience is required. Proficiency in Excel, Word, Outlook, Internet and word processing/typing required. Requires the ability to handle confidential materials; prioritize and handle multiple assignments simultaneously; excellent communication and organizational skills and attention to detail. Ability to work independently, communicate effectively with patients, employees, study sponsor and their designees required.

Reference Number: 40-25679

Salary Grade: 025/ 026

Employment Type: Exempt

Org: SU-Surgery Administration

Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.

Job Family: I-Technical/Professional Research