Clinical Research Assistant

Job Description - Clinical Research Assistant (2400027E)DescriptionThe Clinical Research Assistant performs a variety of research, data, and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations, and Food and Drug Administration (FDA) regulations. In this role, the Clinical Research Assistant completes tasks including identifying eligible participants under the supervision of a senior research team member, preparing necessary documents, equipment, supplies, etc. for research visits, and conducting and documenting visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments, and Standard Operating Procedures (SOPs) for minimal risk studies or for other studies.QualificationsMinimum EducationBachelor's Degree BA/BS degree in a science, technical, health-related field or another applicable discipline. (Required)Minimum Work Experience0 years Experience working in a medical or scientific research setting (Preferred)Functional AccountabilitiesResponsible Conduct of ResearchConsistently demonstrates adherence to the standards for the responsible conduct of research.Plans, conducts, and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.Stays informed of and adheres to institutional policies and federal regulations regarding human subjects research and use of protected health information.Uses research funds and resources appropriately.Maintains confidentiality of data as required.Meets all annual job-related training and compliance requirements.Research AdministrationMaintains knowledge and comprehension of assigned research protocols, including study procedures, timelines, and eligibility.Accurately creates, completes, maintains, and organizes study documents.Accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s), and participation incentives.Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.Attends study meetings, which could include overnight travel, as requested by principal investigator.Works well with other members of the research team and seeks and provides input when appropriate.Adheres to the IRB-approved recruitment plan.Identifies participants that meet eligibility requirements under the supervision of a senior research team member.Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.Interacts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.Engages participants/LARs in the informed consent process according to institutional policies.Follows procedures for documenting participant incentive distribution.Study ManagementPlans, conducts, and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.Conducts and documents visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments, and SOPs for minimal risk studies or for other studies under direction.Completes accurate IRB submissions within institutional timeframes.Records participant visits in the appropriate tracking system.Anticipates study needs and subject caseload in order to meet organizational objectives and deadlines in a timely manner.Data CollectionEnsures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate, and Complete).Ensures that queries are resolved within sponsor and institutional timelines.Plans and performs research specimen collection, labeling, and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.Anticipates and responds to customer needs; follows up until needs are met.Teamwork/CommunicationDemonstrate collaborative and respectful behavior.Partner with all team members to achieve goals.Receptive to others’ ideas and opinions.Performance Improvement/Problem-solvingContribute to a positive work environment.Demonstrate flexibility and willingness to change.Identify opportunities to improve clinical and administrative processes.Make appropriate decisions, using sound judgment.Use resources efficiently.Search for less costly ways of doing things.SafetySpeak up when team members appear to exhibit unsafe behavior or performance.Continuously validate and verify information needed for decision making or documentation.Stop in the face of uncertainty and takes time to resolve the situation.Demonstrate accurate, clear, and timely verbal and written communication.Actively promote safety for patients, families, visitors, and co-workers.Attend carefully to important details - practicing Stop, Think, Act, and Review in order to self-check behavior and performance.Primary Location : District of Columbia-WashingtonWork Locations : CN Hospital (Main Campus) 111 Michigan Avenue NW Washington 20010Job : ResearchOrganization : COE Hospital-Based SpecialtiesPosition Status : R (Regular) - FT - Full-TimeShift : DayWork Schedule : 830 - 5Job Posting : Sep 4, 2024, 6:07:45 PMFull-Time Salary Range : 42702.4 - 71156.8

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