Clinical Research Coordinator
Posted on: May 28, 2023
This position is responsible for all aspects of candidate recruitment and enrollment for clinical research trials. On a day to day basis they'll be expected to identify patients who meet study criteria and develop an enrollment strategy to capture qualified candidates into research trials. They'll be conducting community outreach as well to identify patients that otherwise wouldn't be found in the patient population. Once candidates have confirmed interest in enrolling in a study, Research Coordinators will create a Case Report Form and meet with the patients to provide the informed consent documents and orient patients to the trial schedule and manage expectations regarding timelines and course of therapy. They'll work directly w/Research Nurses, PI's and Data Managers to effectively put patients through the trial.
Client PD: Key tasks include but are not limited to: case-finding, evaluation & abstraction of source documentation, case report form completion, database use & management, data abstraction & organization for presentation/publication. Utilizes multiple data capture/retrieval systems & interacts with variety of health care delivery systems to identify, track, evaluate, collate, analyze & submit subject data. Data may include but is not limited to paper data, electronic data & biological specimens. Collaborates closely with clinical research team, which may include Principal Investigator (PI), to
ensure that key federal/state/local regulatory requirements are followed; that institutional operational research objectives are met; and that ethical obligations are kept. Develops, establishes and maintains productive relationships with the colleagues, all customers and contacts at affiliate sites to achieve essential research outcomes.
IRB, Regulatory, Patient Enrollment, Recruitment, EDC, Oncology, Cancer, Clinical Trials, FDA, Community Outreach, Case Report Form, CRF, Informed Consent, Cancer Center, Comprehensive, patient recruitment, data management, clinical research, clinical trial
Top Skills Details:
IRB,Regulatory,Patient Enrollment,Recruitment,EDC,Oncology,Cancer,Clinical Trials,FDA,Community Outreach,Case Report Form,CRF,Informed Consent,Cancer Center,Comprehensive
Additional Skills & Qualifications:
2+ years of research coordination experience
Independent judgment and critical-thinking skills. Discretionary decision-making skills. Ability to multitask and prioritize autonomously. Excellent written & oral communications skills. Ability to work in a fast paced, demanding environment and adapt to changing priorities.
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The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Keywords: Actalent, Richmond , Clinical Research Coordinator, Healthcare , Richmond, Virginia
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