Clinical Research Coordinator

Highlands Oncology Group PA in; Springdale (AR); On-site; USD 60,000 - 75,000; Full time

Job summary

Join a leading oncology team as a Clinical Research Coordinator where you will manage subjects enrolled in clinical trials, ensuring compliance with regulations and protocols. This position is essential in advancing cancer treatment and supporting patients as they navigate their journey through clinical research.

Qualifications

• Experience managing subjects in clinical trials.
• Familiarity with regulatory compliance and data management.
• Ability to collaborate with clinical staff and study personnel.

Responsibilities

• Screen potential study patients based on protocol.
• Coordinate study subject visits and data collection.
• Report adverse events to the Principal Investigator.

Skills

Compliance with Good Clinical Practice

Data Management

Patient Interaction

Collaboration

Clinical Trial Protocol

Job description

Clinical Research Coordinator (Project Management)

Join our world-class team and help bring cancer treatment HOME!

Highlands Oncology, founded in 1996, aims to transform oncology care in our community. Our founders, Dr. Malcolm Hayward, Dr. Dan Bradford, and Dr. Thad Beck, believed that patients recover better at home, in their community, surrounded by support. From a single location, Highlands has expanded over 26 years to six locations across Northwest and Northcentral Arkansas, employing over 800 team members.

As the region grows, so does the need for comprehensive services and providers. Highlands Oncology is dedicated to staying at the forefront of cancer care, offering a unique, multidisciplinary team that treats patients like family.

Job Summary:

The Clinical Research Coordinator (CRC) is responsible for managing subjects enrolled in clinical trials, ensuring compliance with Good Clinical Practice guidelines, Highlands policies, and sponsor requirements within their assigned setting.

Job Duties / Responsibilities:

1. Screen potential study patients based on protocol inclusion/exclusion criteria.
2. Meet with study subjects and schedule visits according to protocol requirements.
3. Report adverse events to the Principal Investigator and sponsor.
4. Obtain and complete data for study subjects; collaborate with the Research Data Manager to ensure data accuracy.
5. Complete case reports and maintain records for each study subject; ensure data entry into the electronic data capture (EDC) system.
6. Meet with Clinical Research Associates and sponsor representatives.
7. Collaborate with Investigators, mid-level providers, nurses, and other CRCs to identify and document toxicity and adverse events.
8. Serve as a resource to hospital and clinic personnel regarding research activities.
9. Limited travel may be required for investigator meetings, educational opportunities, and to affiliated facilities.

For Level III CRCs: typically, a 10% increase in workload is expected, along with responsibilities in training and mentoring.