{"schemaVersion":"jobsearcher.job.v1","id":"c8c512d9ee4a5569e7752909","url":"https://jobsearcher.com/jobs/c8c512d9ee4a5569e7752909","canonicalUrl":"https://jobsearcher.com/jobs/c8c512d9ee4a5569e7752909","title":"Clinical Research Assistant: Study Data & Protocol Support","description":"Clinical Research Assistant job at Ctr Clinical & Community Rsrch. Silver Spring, MD. Description\nThe 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. Qualifications\nMinimum Education\nBachelor's Degree BA/BS degree in a science, technical, health-related field or another applicable\ndiscipline. (Required) Or\nMinimum Work Experience\n0 years Experience working in a medical or scientific research setting (Preferred) Functional Accountabilities\nResponsible Conduct of Research Consistently demonstrates adherence to the standards for the responsible conduct of research.\nPlans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.\nStays informed of and adheres to institutional policies and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information.\nUses research funds and resources appropriately.\nMaintains confidentiality of data as required.\nMeets all annual job-related training and compliance requirements.\nResearch Administration\nMaintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.\nAccurately creates, completes, maintains and organizes study documents.\nAccounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.\nUses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.\nAttends study meetings, which could include overnight travel, as requested by principal investigator.\nWorks well with other members of the research team and seeks and provides input when appropriate.\nParticipant Enrollment\nAdheres to the IRB-approved recruitment plan.\nIdentifies participants that meet eligibility requirements under the supervision of a senior research team member.\nScreens subjects for eligibility per the protocol and institutional policies.\nCommunicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.\nInteracts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.\nEngages participants/LARs in the informed consent process according to institutional policies.\nFollows procedures for documenting participant incentive distribution.\nStudy Management\nPlans, 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.\nConducts 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.\nCompletes accurate IRB submissions within institutional timeframes.\nRecords participant visits in the appropriate tracking system.\nAnticipates study needs and subject caseload in order to meet organizational objectives and deadlines in a timely manner.\nData Collection\nEnsures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate and Complete).\nEnsures that queries are resolved within sponsor and institutional timelines.\nPlans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.\nEnsures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.\nAnticipate and responds to customer needs; follows up until needs are met\n\nTeamwork/Communication\nDemonstrate collaborative and respectful behavior\nPartner with all team members to achieve goals\nReceptive to others’ ideas and opinions\n\nPerformance Improvement/Problem-solving\nContribute to a positive work environment\nDemonstrate flexibility and willingness to change\nIdentify opportunities to improve clinical and administrative processes\nMake appropriate decisions, using sound judgment\n\nCost Management/Financial Responsibility\nUse resources efficiently\nSearch for less costly ways of doing things\n\nSafety\nSpeak up when team members appear to exhibit unsafe behavior or performance\nContinuously validate and verify information needed for decision making or documentation\nStop in the face of uncertainty and takes time to resolve the situation\nDemonstrate accurate, clear and timely verbal and written communication\nActively promote safety for patients, families, visitors and co-workers\nAttend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance\nPrimary Location : Maryland-Silver Spring Work Locations : Inventa Towers\n1 Inventa Place\nSilver Spring 20910\nJob : Research Organization : Ctr Clinical & Community Rsrch Position Status : R (Regular)- FT - Full-Time\nShift : Day\nWork Schedule : 9a-5p\nJob Posting : May 15, 2025, 4:47:27 PM Full-Time Salary Range : 42702.4-71156.8\n#J-18808-Ljbffr","company":"Payfuture Technologies","rawCompany":"payfuture technologies","city":"Silver Spring","state":"MD","isRemote":false,"isActive":true,"createdAt":"2026-06-20T03:55:40.179Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"19-4061.00","title":"Social Science Research Assistants","slug":"social-science-research-assistants"},{"code":"31-9099.00","title":"Healthcare Support Workers, All Other","slug":"healthcare-support-workers-all-other"}],"industries":[{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Clinical Research Assistant: Study Data & Protocol Support","description":"Clinical Research Assistant job at Ctr Clinical & Community Rsrch. Silver Spring, MD. Description\nThe 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. Qualifications\nMinimum Education\nBachelor's Degree BA/BS degree in a science, technical, health-related field or another applicable\ndiscipline. (Required) Or\nMinimum Work Experience\n0 years Experience working in a medical or scientific research setting (Preferred) Functional Accountabilities\nResponsible Conduct of Research Consistently demonstrates adherence to the standards for the responsible conduct of research.\nPlans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.\nStays informed of and adheres to institutional policies and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information.\nUses research funds and resources appropriately.\nMaintains confidentiality of data as required.\nMeets all annual job-related training and compliance requirements.\nResearch Administration\nMaintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.\nAccurately creates, completes, maintains and organizes study documents.\nAccounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.\nUses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.\nAttends study meetings, which could include overnight travel, as requested by principal investigator.\nWorks well with other members of the research team and seeks and provides input when appropriate.\nParticipant Enrollment\nAdheres to the IRB-approved recruitment plan.\nIdentifies participants that meet eligibility requirements under the supervision of a senior research team member.\nScreens subjects for eligibility per the protocol and institutional policies.\nCommunicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.\nInteracts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.\nEngages participants/LARs in the informed consent process according to institutional policies.\nFollows procedures for documenting participant incentive distribution.\nStudy Management\nPlans, 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.\nConducts 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.\nCompletes accurate IRB submissions within institutional timeframes.\nRecords participant visits in the appropriate tracking system.\nAnticipates study needs and subject caseload in order to meet organizational objectives and deadlines in a timely manner.\nData Collection\nEnsures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate and Complete).\nEnsures that queries are resolved within sponsor and institutional timelines.\nPlans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.\nEnsures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.\nAnticipate and responds to customer needs; follows up until needs are met\n\nTeamwork/Communication\nDemonstrate collaborative and respectful behavior\nPartner with all team members to achieve goals\nReceptive to others’ ideas and opinions\n\nPerformance Improvement/Problem-solving\nContribute to a positive work environment\nDemonstrate flexibility and willingness to change\nIdentify opportunities to improve clinical and administrative processes\nMake appropriate decisions, using sound judgment\n\nCost Management/Financial Responsibility\nUse resources efficiently\nSearch for less costly ways of doing things\n\nSafety\nSpeak up when team members appear to exhibit unsafe behavior or performance\nContinuously validate and verify information needed for decision making or documentation\nStop in the face of uncertainty and takes time to resolve the situation\nDemonstrate accurate, clear and timely verbal and written communication\nActively promote safety for patients, families, visitors and co-workers\nAttend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance\nPrimary Location : Maryland-Silver Spring Work Locations : Inventa Towers\n1 Inventa Place\nSilver Spring 20910\nJob : Research Organization : Ctr Clinical & Community Rsrch Position Status : R (Regular)- FT - Full-Time\nShift : Day\nWork Schedule : 9a-5p\nJob Posting : May 15, 2025, 4:47:27 PM Full-Time Salary Range : 42702.4-71156.8\n#J-18808-Ljbffr","datePosted":"2026-06-20T03:55:40.179Z","dateModified":"2026-06-20T03:55:40.179Z","hiringOrganization":{"@type":"Organization","name":"Payfuture Technologies","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Silver Spring","addressRegion":"MD","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c8c512d9ee4a5569e7752909"},"url":"https://jobsearcher.com/jobs/c8c512d9ee4a5569e7752909"}}