Description:

　　This position is responsible for all aspects of clinical data management and patient data accuracy for clinical research trials. On a day to day basis they'll be expected to work directly w/the Clinical Research Coordinators to inventory all patient data captured by the Coordinators and confirm accuracy and quality assurance. Candidates will review multiple case report forms and query for accuracy. They'll also work directly w/Research Nurses, PI's to effectively put patients through the trial and have their data updated and accurate.

　　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 VCU colleagues, all customers and contacts at affiliate sites to achieve essential research outcomes.

　　Skills:

　　Data management, Crf design, Data, IRB, Regulatory, EDC, Oncology, Cancer, Clinical Trials, FDA, Case Report Form, CRF, Informed Consent, Electronic Data Capture, Clinical Data Management, Clinical Data Manager, Quality Assurance, Quality Control, Data Enry

　　Additional Skills & Qualifications:

　　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 client status, regulations and work environment. Detail-oriented organizational skills. Highly proficient with multiple computer applications, including but not limited to: Microsoft Word, Microsoft Excel, spreadsheet management, PDF file creation/use, online database use/maintenance, internet-based research, network & online file maintenance & management, and custom report generation. Demonstrated knowledge of medical terminology.

　　Preferred: Experience with interpreting complex protocols, subject records and federal, state, local regulations preferred. Experience using health-care based clinical information systems preferred. Bachelor’s degree and experience in health research and/or healthcare-related field preferred, or an equivalent combination of training & experience.

　　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.