Research Associate - (Oncology)

UPMC•Pittsburgh, PA

5h•Onsite

About The Position

UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Associate - Oncology to support the Clinical Research Services team. This role will float and support various Oncology Disease Center program studies. The Clinical Research Services (CRS) team facilitates the development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman. These trials include institutional, multi-center cooperative group/National Clinical Trial Network (NCTN), consortium, and industry-sponsored trials. CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing. Under the direction of the Clinical Research Manager, the research associate will work with physicians, nurses, and allied health professionals to facilitate clinical research trials and independently execute job functions related to protocol management. This position is part of a UPMC Research Career ladder, and the incumbent will be hired into the appropriate level based on their current education and experience.

Requirements

High school diploma or equivalent required.
Bachelor’s degree in healthcare or related field OR four (4) years of experience in clinical research and/or related setting OR three (3) years of experience in clinical research with certification.
Prior knowledge and use of Microsoft Office software produces.
Ability to work with a PC database application.
Act 34 Criminal Clearance

Nice To Haves

Preferred knowledge of research methodology
Prior supervisory and or/ project management experience preferred.
Oncology and/or Research experience preferred.

Responsibilities

Assists in entering subject trial registration and study status updates into CTMA.
Assists in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor.
Assists in verifying subject eligibility according to protocols by reviewing medical records, laboratory, and radiology or CT scan results.
Create study-specific source documents, case report forms and study visit checklists.
Ensures that patient's records, slides, radiology tests, lab work results, etc. are obtained and reviewed prior to patient entry into a study.
Performs consenting process and study implementation of lab, registry, and non-therapeutic clinical trials.
Process required documents as need for the research protocols.
Responsible for prompt and accurate data collection for protocols.
Shares responsibility of managing the day-to-day activities for the research protocols.
Will serve as an assistant to support all main functions of the department.