HRI offers a competitive salary and comprehensive benefits package.
Description of Duties:
The Clinical Research Associate I will support the clinical research mission of the Institute and Clinical Research Services (CRS) through the review and processing of detailed regulatory documents (protocols, consents, manuals etc) for research teams - principal investigators, clinical research coordinators after IRB approval. Tracks, reports and communicates to various staff/departments the status of study specific requirements. Ensures all the applicable documents are posted on a Clinical Research Services internal website and enters study information into databases.
Applicants must minimally have an Associate’s degree in a health or science related field. The preferred candidate will have a Bachelor's degree in health science, certified clinical research professional through SoCRA, ACRP or similar clinical research organization, two years of clinical research experience, previous regulatory research experience, proficient skills in MS Office programs especially Word, and excellent verbal and written communication. The candidate will pay attention to detail and have the ability to multi-task in a busy environment. Suitable for a candidate that enjoys working in fast-paced, deadline driven environment.
This is a grant-funded position. Compliance with funding requirements such as time and effort reporting, grant deliverables, and contract deliverables is required.
Health Research Incorporated (HRI) Roswell Park Division participates in the E-Verify program.
Affirmative Action/Equal Opportunity Employer/Qualified Individuals with Disabilities/Qualified Protected Veterans
Applicants must reference the Posting # when applying for this position.
Interested applicants may apply by uploading a cover letter and resume below in Microsoft Word or PDF format.