This role will coordinate research in an exciting new environment, with the full backing of a new type of research architecture and a top-tier technology team.
\nThe ideal candidate will have a track record of excellence as a Research Assistant or CRC or other similar role, including developing successful relationships with providers.
\nKey responsibilities include:\nActing as senior study coordinator to execute trials conducted within physician practices,\nConducting patient recruitment and enrollment of eligible patients,\nLeading patient study visits, which may also include clinical and lab procedures,\nIndependently administering the informed consent process with care and quality,\nEnsuring protocol adherence and high data integrity,\nProviding high quality source data capture and documentation,\nSupporting study start-up and planning, including PSVs and SIVs,\nFacilitating monitoring visits (IMVs) and sponsor correspondence,\nManaging the follow-up process,\nIP management, dispensation and accountability,\nAdverse Event management, tracking, and follow-up,\nData entry to CRF/EDC and query resolution in a timely manner,\nSupporting study close-out, including COVs,\nProtocol deviation tracking, reporting, and reconciliation,\nTraining and mentoring junior research staff,\nUsing and helping improve Topography’s proprietary tool set,\nUnderstanding and complying with all regulations, policies, and guidelines applicable to clinical research, including our SOPs,\nEnsuring adherence to study protocols while ensuring trial staff maintain meticulous accuracy in completing all documentation,\nConducting Quality Control activities including routine QC checks during and following study visits,\nAny other duties assigned by manager.
\nXML job scraping automation by YubHub
","url":"https://yubhub.co/jobs/job_b5658e2f-c9d","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Topography","sameAs":"https://jointopo.com","logo":"https://logos.yubhub.co/jointopo.com.png"},"x-apply-url":"https://jobs.lever.co/jointopo/5ca87b21-9f36-41e0-b846-4bef140256b4","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Clinical Research Coordinator","Research Assistant","FDA regulations","ICH/GCP guidelines","Data entry","CRF/EDC","Query resolution","Study start-up","Planning","Monitoring visits","Sponsor correspondence","IP management","Dispensation","Accountability","Adverse Event management","Tracking","Follow-up","Quality Control","Regulations","Policies","Guidelines","SOPs"],"x-skills-preferred":[],"datePosted":"2026-04-17T13:05:34.702Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Ann Arbor"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"Clinical Research Coordinator, Research Assistant, FDA regulations, ICH/GCP guidelines, Data entry, CRF/EDC, Query resolution, Study start-up, Planning, Monitoring visits, Sponsor correspondence, IP management, Dispensation, Accountability, Adverse Event management, Tracking, Follow-up, Quality Control, Regulations, Policies, Guidelines, SOPs"}]}