Clinical Research Associate (Casual)

UPMC; Pittsburgh (Allegheny County); On-site; USD 60,000 - 90,000; Full time

Job summary

UPMC Department of Dermatology seeks a Clinical Research Associate to support its clinical research team at the Falk Medical Building, Pittsburgh. The role involves data collection, patient coordination, and ensuring compliance with study protocols.

The ideal candidate has a BA in Business/Healthcare or SOCRA/ACRP certification with clinical research experience and strong MS Office skills. Work hours are M-F, 7:00 a.m.–3:00 p.m., onsite in Pittsburgh.

Qualifications

• B.A. degree in Business, Healthcare, or related or LPN license plus 2 years of clinical research experience.
• Certification through SOCRA or ACRP with 2 years clinical research experience is acceptable.
• Knowledge and use of MS Office and PC database applications.

Responsibilities

• Create individualized study calendars and review them with the patient.
• Meet with the principal investigator and Clinical Research Coordinator to review patient status.
• Ensure prompt and accurate data collection for protocols.
• Assist in preparing, sending and tracking documents for re-consenting patients.
• Participate in multidisciplinary meetings and educational events as required.
• Obtain follow-up data and enter into CTMA; manage study documentation and records.
• Assist with consent forms and ensure informed consent is obtained.
• Monitor enrollment and report subject trial status to the team.
• Facilitate entry of patients onto clinical trials and assist billing with research procedures.
• Perform trial-related responsibilities including sample handling and data collection.

Education

B.A. degree in Business, Healthcare, or related

SOCRA/ACRP certification

Clinical research experience (2+ years)

Tools

MS Office

Job description

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UPMC Department of Dermatology is hiring a Clinical Research Associate to support its clinical research team at the Falk Medical Building, 3601 Fifth Avenue, 5th Floor, Pittsburgh, PA 15213. The hours are Monday through Friday from 7:00 a.m. to 3:00 p.m. and provides an excellent opportunity to contribute to innovative dermatology research.

Responsibilities:

• Create individualized study calendars and reviews them with the patient.
• Meet with the principal investigator and Clinical Research Coordinator/Supervisor to review patient status on as needed basis.
• Responsible for prompt and accurate data collection for protocols.
• Assist coordinator in preparing, sending and tracking documents for re-consenting patients.
• Participate in multi-disciplinary meetings to foster educational development by attending relevant seminars, conferences and sponsored educational events as required.
• In addition, will contact patient/family members to obtain follow up or survival data information after study completion, and will review survival record data bases to provide follow up. All follow up information is to be documented onto study CRFs and entered into CTMA.
• Assist in providing consent forms to coordinators and investigators so that the informed consent process is implemented with study subjects.
• Meet monthly with disease center research program leader and research team to present subject trial status.
• Facilitate entry of patient on to clinical trials by performing the following tasks.
• Complete research requisitions to assist billing department to prevent billing of research procedures to third party payers.
• Perform consenting process and study implementation of lab, registry, and non-therapeutic clinical trials.
• Perform trial related responsibilities as required such as processing, storing and shipping trial specimens, administers study related questionnaires to study participants (i.e. quality of life, etc.).
• Assist in entering subject trial registration and study status updates into CTMA.
• Insure that patient's records, slides, radiology tests, lab work results, etc. are obtained and reviewed prior to patient entry onto a study.
• Assist in verifying subject eligibility according to protocols by reviewing medical records, laboratory, and radiology or CT scan results.
• Complete financial review forms of potential patients to determine insurance coverage for standard of care procedures and completion of requisition forms.
• Create study specific source documents, case report forms and study visit checklists.
• Facilitate the enrollment of subjects to trials open to the community network sites and will follow up on outstanding data collections.
• Facilitate follow-up of protocol patients by developing maintenance-therapy data collection sheets for all protocol patients who require follow-up.
• Assist in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor.
• Monitor subject compliance of oral study medications.
• Assist with obtaining tumor measurements from Radiologist or Investigators to determine response information as per protocol.
• B.A. degree in Business, Healthcare, or related orLPN license minimum of 2 years of clinical research experience
• orHigh school graduate with current certification as a Clinical Research Associate from either the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) along with a minimum of two years of clinical research experience
• Knowledge and use of MS office software products and the ability to work with PC database applications.
• Excellent organizational skills and be able to work on projects/tasks simultaneously.
• Highly motivated and be able to work with minimal supervision.
• Ability to adapt to multiple organizational structures.
• Ability to meet deadlines and be flexible in response to sudden workload changes.Licensure, Certifications, and Clearances:
• Act 34

UPMC is an Equal Opportunity Employer/Disability/Veteran