Description:

　　3 YEARS CRC EXPERIENCE REQUIRED

　　JOB DESCRIPTION: Coordinates implements and evaluates clinical research trials, studies and projects. Provides direction in the development of research protocols. Recruits and screens potential study participants, and develops and conducts patient and family education accordingly. Oversees financial accounts to ensure operations remain within approved levels. Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures. Makes referrals to in-house or community professionals and serves as clinical resource. Collects data, assists in developing data collection systems and compiles reports.

　　Provides direction and may support other Research Coordinators or other support members. Performs related responsibilities as required.

　　• Independently manages significant and key aspects of Oncology related trials including one or more small trials, or research projects.

　　• Operate as Oncology Research Coordinator in support of specified Oncology disease group(s)

　　• Perform required Patient consents

　　• Trains and provides guidance to less experienced staff.

　　• Oversees data management for research projects.

　　• Interfaces with research participants and resolves issues related to study protocols

　　• Authorizes purchases for supplies and equipment maintenance.

　　• Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.

　　• Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.

　　• Monitors IRB submissions and responds to requests and questions.

　　• Interfaces with study sponsors, monitors and reports SAEs; resolves study queries.

　　• Provides leadership in determining, recommending, and implementing improvements to policies/processes.

　　• Assists in developing grant proposals and protocols.

　　• With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics.

　　• May perform some supervisory duties.

　　• Performs related approved responsibilities as required.

　　Skills:

　　Oncology, CCRC, Research Coordinator, GCP, CRF, ICF, patient consenting, regulatory, RN, BSN, Nurse, Clinical research, Crc

　　Top Skills Details:

　　Oncology,CCRC,Research Coordinator,GCP,CRF,ICF,patient consenting, regulatory,RN,BSN,Nurse

　　Additional Skills & Qualifications:

　　MINIMUM QUALIFICATIONS: 3 years of clinical research coordinator experience, specifically working on oncology trials

　　Experience Level:

　　Intermediate Level

　　Diversity, Equity & Inclusion

　　At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

　　Hiring diverse talent

　　Maintaining an inclusive environment through persistent self-reflection

　　Building a culture of care, engagement, and recognition with clear outcomes

　　Ensuring growth opportunities for our people

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.