{"id":3034571,"url":"https://alion.io/job/copyright-axle-informatics-research-nurse","title":"Research Nurse","company":{"id":4416199,"name":"Copyright Axle Informatics","domain":"axleinfo.com","url":"https://alion.io/company/axleinfo","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"B","score":80,"open_postings":9,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":10,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bethesda, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":100000,"max":110000,"currency":"USD","period":"year","gross":null,"usd_annual":110000},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-15T17:14:37Z","employer_posted_date":"2026-10-15","last_verified_at":"2026-11-01T04:12:03Z","board_verified":true,"closed_at":null,"days_open":16,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":16},"description":"(ID: 2026-3821)\nAxle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).\nAxle is seeking a Research Nurse to join our vibrant team at the National Institutes of Health (NIH) supporting the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) located in Bethesda, Maryland.\nBenefits We Offer:\n100% Medical, Dental & Vision Coverage for Employees\nPaid Time Off and Paid Holidays\n401K match up to 5%\nEducational Benefits for Career Growth\nEmployee Referral Bonus\nFlexible Spending Accounts:Healthcare (FSA)\nParking Reimbursement Account (PRK)\nDependent Care Assistant Program (DCAP)\nTransportation Reimbursement Account (TRN)\n\nPosition Information:\nUnder this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute of Diabetes and Digestive and Kidney Diseases. The primary objective is to provide services and deliverables through performance of support services.\nAdditional Qualifications:\nCertifications & Licenses\nMinimum of two (2) years of nursing experience with CPR certification\n\nMaster’s degree in nursing with current state licensure as a Registered Nurse.\n\nThree (3) years specialized experience plus a bachelor’s degree is equivalent to a master’s degree\n\nField of Study\nNursing\n\nSoftware\nMS Office Suite\n\nSkills\nExperience working on clinical Protocols\n\nStrong diagnostic and clinical skills\n\nExcellent analytical, organizational and time management skills\n\nStrong verbal and written communication skills\n\nExperience with MedSurg Nursing\n\nDeliverables:\nWork products and documents related to recruitment and retention of patients into specific clinical protocols; ensure protocol compliance and database management; educate patients regarding the nature of the disease process and possible therapeutic strategies and protocol objectives. - Daily\n\nWork products and documents related to collect relevant clinical data such as laboratory test results and social background; interview patients to obtain history; maintain computerized patient files and databases; interpret data; identify results that merit prompt clinical action; maintain required documentation and files for research protocols. - Ad-Hoc\n\nWork products and documents related to performing physical assessments; analyze trends in patient conditions; suggest possible alterations in treatment regimens; perform physical assessments of patients; analyze trends in patient conditions; suggest possible alterations in treatment regimens according to research protocols. - Ad-Hoc\n\nWork products and documents related to examining and monitoring patients during protocol studies; ensure the collection of a complete clinical database on each patient; participate in scheduled clinical update lectures, meetings and grand rounds; respond to telephone inquiries from protocol patients. - Ad-Hoc\n\nWork products and documents related to providing counseling and teaching for patients and their families as appropriate; determine appropriate diagnostic testing; gather data for yearly IRB reviews; coordinate the submission process. - Ad-Hoc\n\nWork with staff on prescheduling the appropriate evaluations, arranging patient travel and providing the patient with confirmation of the appointment time and a list of the scheduled diagnostic testing; schedule appropriate medical consultations as necessary. - Ad-Hoc\n\nWork products and documents related to participating in the patient care conference; assemble diagnostic studies; attend professional meetings and seminars; review and summarize relevant literature. - Ad-Hoc\n\nClean Equipment - Ad-Hoc\n\nRun Validation - Ad-Hoc\n\nInspect Equipment - Ad-Hoc\n\nMeet with lab members to present updates - Ad-Hoc\n\nStatement of Work Details:\nOrganize and facilitate the training program and teach physicians, physicians in training, nurses and other staff. - 1\n\nMentor health care members in the execution of trials and resolution of logistical constraints and update team members of changing directions in study implementation. - 2\n\nProvide training to clinic staff with regard to Investigator, brochure information, protocol implementation, general and specific data collection and research practices. - 3\n\nProvide mentorship developing skills and expertise in research protocols and all aspects of clinical research. - 4\n\nProvide mentorship to nurse specialists to develop skills and expertise in program areas. - 5\n\nRecruits and screens patients for inclusion in protocols and clinical trials.\n\nAssist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol.\n\nParticipate in recruitment and outreach activities and contribute to recruitment strategies through innovative ideas.\n\nRecruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol.\n\nDesign and maintain a selection of materials appropriate to send to health care referral sources seeking eligibility information or other objectives.\n\nOrganize and maintain an active referral list and master schedule for planning follow up and new patient admissions.\n\nProvide instruction to potential clinical study subjects and those involved in care of subjects on aspects of subject’s care, treatments, and side-effects.\n\nProvide information about the study to referring physicians, advocacy groups, NIH offices, and in response to inquiries from potential study participants.\n\nPerforms assessments and physicals and collects medical histories.\n\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.\n\nObtain and record complete health histories and conduct physical assessments; communicate data from these and other sources.\n\nManage clinical and research support activities to ensure patient safety and address the clinical needs of the patients.\n\nReview findings from assessments and other sources in clinical rounds.\n\nReview charts to collect relevant clinical data such as laboratory test results and social background.\n\nComplete medical and psychiatric assessments of potential participants in multiple research protocols by collecting and reviewing past and present medical records and conduct interviews with research applicants and their families.\n\nConduct family interviews to obtain comprehensive understanding of the care needs of the patient.\n\nContinually assess ongoing understanding of the research process for patients and families and provide teaching and support as indicated.\n\nAdministers protocol consents and documentation and monitors compliance.\n\nEnsure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks.\n\nCollaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol.\n\nContribute to all study related IRB and regulatory matters, including all reporting requirements (including deviations, unanticipated problems, adverse events) and report issues and variance promptly to the research team.\n\nCollect and report data to appropriate regulatory and monitoring agencies.\n\nPerform quality assurance and quality control activities relating to protocol adherence, protocol monitoring, data collection, data abstraction and data analysis and protect research participant data in accordance with regulatory requirements.\n\nCoordinate various activities to ensure proper and filing of serious adverse events, amendments, annual reports, and other regulatory documents.\n\nPrepare documentation and track and report regulatory and institutional protocol requirements and resolve all stipulations from protocol oversight groups.\n\nPerforms data input and management.\n\nPerform accurate data entry into research database, including the use of standardized scales and assessments.\n\nParticipate in data analysis and management as well as manuscript preparation and presentation of findings.\n\nMaintain computerized patient files and databases containing research data generated through protocol studies and perform data searches of medical records for analyses of patient characteristics.\n\nSupport the general implementation, tracking, data acquisition, collection and reporting of all elements of the protocols.\n\nManage data through research databases to ensure accurate and reliable data entry.\n\nExamine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient.\n\nProvide expertise in clinical trial coordination and management of data acquisition.\n\nPerforms clinical data interpretation and evaluates and interprets protocol and clinical trial findings.\n\nDocument observations and identify and evaluate trends and important findings, communicating information to the multidisciplinary research team for prompt clinical action.\n\nMonitor activities pertaining to clinical protocols such as monitoring patient recruitment and retention, trial progress, and the need for extension or renewal of ongoing trials.\n\nPresent clinical data in terms which may be understood by the patient, as well as, interpretation at a level which is conversant with other health professional including physicians.\n\nDevelop intake tools and screening forms and work with researchers and medical staff on the general administration of protocols’ implementation.\n\nCollaborate with staff to analyze and evaluate current systems of health care delivery and to identify and implement new practice patterns.\n\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.\n\nProblem-solve complex or unpredictable situations and improve processes and services to patients and colleagues. Participates in training and mentoring new staff.\n\nDevelops new research protocols.\n\nParticipate in the design and implementation of current and future protocols and studies.\n\nSurvey the medical literature for background information on specific aspects of the diseases under purview.\n\nDesign, implement and evaluate complex protocols and manage challenging patient populations and assist with document preparations and processes.\n\nDevelop new standards for novel and unpredicted research situations and interventions.\n\nUtilize established resources to design new study methods to meet research study objectives.\n\nWork with staff on drafting of new protocol amendments and associated documents by providing editorial support and expert opinion.\n\nPerform protocol activities including study drug administration, data collection and submission, patient counseling and physical assessment.\n\nMaintain contact with patients and referring physicians to explain patient’s conditions and symptoms; interpret results of laboratory tests; discuss the future status of patients who have participated in the study.\n\nInterface with the inpatient and outpatient unit staffs to assess patient concerns and facilitate compliance with protocol studies.\n\nExamine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient.\n\nEnsure that protocol and regulatory requirements are met in terms of...","description_format":"text","description_chars":16416,"description_truncated":true,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":["401k plan"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Artificial Intelligence","Machine Learning"],"lifecycle":[{"event":"open","at":"2026-10-21T21:07:18Z"}],"visa":[],"liveness":{"score":29,"band":"fade","label":"Fading","p_open":1,"p_active":0.639,"p_room":0.45,"age_days":16,"expected_fill_days":10,"reasons":["conf:1","velocity","win:tail","comp:junior"],"computed_at":"2026-11-01T06:10:25Z"},"pay":{"stated_usd_annual":110000,"is_top_pay":true},"html_url":"https://alion.io/job/copyright-axle-informatics-research-nurse","json_url":"https://alion.io/job/copyright-axle-informatics-research-nurse.json","meta":{"generated_at":"2026-11-01T07:01:36Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":10946,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-02T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":4416199},"rest":"https://alion.io/mcp/rest/get_company?id=4416199"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fcopyright-axle-informatics-research-nurse"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fcopyright-axle-informatics-research-nurse"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fcopyright-axle-informatics-research-nurse"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/copyright-axle-informatics-research-nurse\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fcopyright-axle-informatics-research-nurse"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3034571}},{"tool":"search_jobs","arguments":{"company":"axleinfo.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3034571},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); 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