{"schemaVersion":"jobsearcher.job.v1","id":"e2d2b5df1fb66740093225f1","url":"https://jobsearcher.com/jobs/e2d2b5df1fb66740093225f1","canonicalUrl":"https://jobsearcher.com/jobs/e2d2b5df1fb66740093225f1","title":"Research Nurse","description":"Job Description:\n\nConcentric Methods is seeking a Research Nurse to join our team in Baltimore, MD in support of the NIH.\nResponsibilities:\nRecruits and screens patients for inclusion in protocols and clinical trials.\nAssist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol\nRecruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol\nProvide instruction to potential clinical study subjects and those involved in care of subjects on aspects of subjects care, treatments, and side-effects\nPerforms assessments and physicals, and collects medical histories.\nParticipate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research\nObtain and record complete health histories and conduct physical assessments; communicate data from these and other sources\nManage clinical and research support activities to ensure patient safety and address the clinical needs of the patients\nAdministers protocol consents and documentation and monitors compliance.\nEnsure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks\nCollaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol\nPerforms data input and management.\nPerform accurate data entry into research database, including the use of standardized scales and assessments\nExamine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient\nPerforms clinical data interpretation and evaluates and interprets protocol and clinical trial findings.\nParticipate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs\nParticipates in training and mentoring new staff\nProvide mentorship developing skills and expertise in research protocols and all aspects of clinical research\nDevelops new research protocols\nWork with staff on drafting of new protocol amendments and associated documents by providing editorial support and expert opinion\n\nJob Requirements:\n\nAssociate’s degree in Nursing with current state nursing license.\nMinimum of 2 years of nursing experience with CPR certification.\nExperience in a clinical research environment.\nKnowledge of clinical research data collection and clinical data report preparation.\nWorking knowledge of ICH-GCPs.\nKnowledge of the principles, theories, techniques and practices of general nursing.\nDemonstrated expertise in data management.\nAbility to coordinate various activities (research subject schedules, data and biospecimen collection and nursing care) to ensure proper and timely filing of standard clinical/regulatory documentation, serious adverse events, amendments, annual reports and other regulatory documents.\nAbility to participate in efforts to ensure scientific quality and human subjects’ protection.\nAbility to oversee ongoing protocol operations to ensure study compliance; troubleshoot possible protocol violations.\nKnowledge of Microsoft Office Suite (MS Word, Excel, Outlook) and other spreadsheet applications.\nStrong communications skills, both oral and written.\nExcellent analytical, organizational and time management skills.\nThe total hourly pay for this exempt position is $45.00/hr. to $50.00/hr. for up to 40 hours per week. This rate represents the company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.\n\nCape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.","company":"Concentric Methods","rawCompany":"concentric methods","city":"Baltimore","state":"MD","isRemote":false,"isActive":false,"createdAt":"2026-08-03T23:32:45.628Z","occupations":[{"code":"29-1141.00","title":"Registered Nurses","slug":"registered-nurses"},{"code":"29-1141.01","title":"Acute Care Nurses","slug":"acute-care-nurses"},{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"}],"industries":[{"code":"622110","title":"General Medical and Surgical Hospitals","slug":"general-medical-and-surgical-hospitals"},{"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":"622310","title":"Specialty (except Psychiatric and Substance Abuse) Hospitals","slug":"specialty-except-psychiatric-and-substance-abuse-hospitals"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Research Nurse","description":"Job Description:\n\nConcentric Methods is seeking a Research Nurse to join our team in Baltimore, MD in support of the NIH.\nResponsibilities:\nRecruits and screens patients for inclusion in protocols and clinical trials.\nAssist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol\nRecruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol\nProvide instruction to potential clinical study subjects and those involved in care of subjects on aspects of subjects care, treatments, and side-effects\nPerforms assessments and physicals, and collects medical histories.\nParticipate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research\nObtain and record complete health histories and conduct physical assessments; communicate data from these and other sources\nManage clinical and research support activities to ensure patient safety and address the clinical needs of the patients\nAdministers protocol consents and documentation and monitors compliance.\nEnsure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks\nCollaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol\nPerforms data input and management.\nPerform accurate data entry into research database, including the use of standardized scales and assessments\nExamine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient\nPerforms clinical data interpretation and evaluates and interprets protocol and clinical trial findings.\nParticipate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs\nParticipates in training and mentoring new staff\nProvide mentorship developing skills and expertise in research protocols and all aspects of clinical research\nDevelops new research protocols\nWork with staff on drafting of new protocol amendments and associated documents by providing editorial support and expert opinion\n\nJob Requirements:\n\nAssociate’s degree in Nursing with current state nursing license.\nMinimum of 2 years of nursing experience with CPR certification.\nExperience in a clinical research environment.\nKnowledge of clinical research data collection and clinical data report preparation.\nWorking knowledge of ICH-GCPs.\nKnowledge of the principles, theories, techniques and practices of general nursing.\nDemonstrated expertise in data management.\nAbility to coordinate various activities (research subject schedules, data and biospecimen collection and nursing care) to ensure proper and timely filing of standard clinical/regulatory documentation, serious adverse events, amendments, annual reports and other regulatory documents.\nAbility to participate in efforts to ensure scientific quality and human subjects’ protection.\nAbility to oversee ongoing protocol operations to ensure study compliance; troubleshoot possible protocol violations.\nKnowledge of Microsoft Office Suite (MS Word, Excel, Outlook) and other spreadsheet applications.\nStrong communications skills, both oral and written.\nExcellent analytical, organizational and time management skills.\nThe total hourly pay for this exempt position is $45.00/hr. to $50.00/hr. for up to 40 hours per week. This rate represents the company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.\n\nCape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.","datePosted":"2026-08-03T23:32:45.628Z","dateModified":"2026-08-03T23:32:45.628Z","hiringOrganization":{"@type":"Organization","name":"Concentric Methods","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Baltimore","addressRegion":"MD","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e2d2b5df1fb66740093225f1"},"url":"https://jobsearcher.com/jobs/e2d2b5df1fb66740093225f1"}}