Clinical Research Coordinator I- School of Medicine, Cardiology Emory UniversityClinical Research Coordinator I- School of Medicine, CardiologyAtlanta, GeorgiaDiscover Your Career at Emory University: Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention Emory UniversityClinical Research Coordinator I - The School of Nursing - Alzheimer's Disease PreventionAtlanta, GeorgiaFull timeDiscover Your Career at Emory University: Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Duties include facilitating all aspects of study visits, performing phlebotomy, cognitive testing, vascular ultrasound, wet lab biospecimen processing and adherence to study protocols.
Clinical Research Coordinator I - School of Medicine, Urology Emory UniversityClinical Research Coordinator I - School of Medicine, UrologyAtlanta, GeorgiaFull timeDiscover Your Career at Emory University: Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Clinical Research Coordinator I School of Medicine, Urology Emory UniversityClinical Research Coordinator I School of Medicine, UrologyAtlanta, GATo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Clinical Research Coordinator I School of Medicine, Nephrology Emory UniversityClinical Research Coordinator I School of Medicine, NephrologyAtlanta, GARemoteTo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Clinical Research Coordinator I The School of Nursing Alzheimer''s Disease Prevention Emory UniversityClinical Research Coordinator I The School of Nursing Alzheimer''s Disease PreventionAtlanta, GARemoteTo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Duties include facilitating all aspects of study visits, performing phlebotomy, cognitive testing, vascular ultrasound, wet lab biospecimen processing and adherence to study protocols.
Manager, Clinical Research Monitoring Edwards Lifesciences CorpManager, Clinical Research MonitoringGA$126,000–$178,000 / yearHow you will make an impact: Providing input on strategic direction on field monitoring of studies and data collection for clinical trials with increased volume and complexity (e.g., KOL site), acting as a Core Team lead, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Leading in the development of technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
Clinical Research Coordinator I School of Medicine (Adult) Psychiatry Emory UniversityClinical Research Coordinator I School of Medicine (Adult) PsychiatryAtlanta, GATo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Senior Specialist, Clinical Research Monitoring Edwards Lifesciences CorpSenior Specialist, Clinical Research MonitoringGA$108,000–$153,000 / yearHow you will make an impact: Field monitoring of studies and data collection for clinical trials, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Developing and delivering technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
Clinical Research Coordinator I School of Medicine, Cardiology Emory UniversityClinical Research Coordinator I School of Medicine, CardiologyAtlanta, GARemoteTo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Clinical Research Coordinator I School of Medicine General Medicine (Part Time) Emory UniversityClinical Research Coordinator I School of Medicine General Medicine (Part Time)Atlanta, GARemoteTo request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322.
Research Assistant - Pathology & Immunology Washington University in St LouisResearch Assistant - Pathology & ImmunologyForest Park, GeorgiaAnimal Restraints, Blood Sampling, Data Analysis, Data Interpretations, Document Research, Flow Cytometry, Genome Editing, Hematology, Immunology, Laboratory Processes, Mouse Handling, Scientific Research, Stem Cell Biology, Verbal Communications, Written Communication Grade . Candidates will have opportunities to contribute to a variety of projects, receive mentorship from the PI and senior researchers in the lab, attend and present at local and international meetings, and interact with collaborators in the WashU Department of Pathology & Immunology and the Division of Oncology in the Department of Medicine.
Associate Director, Biostatistics | School of Medicine - Pediatrics, Innovation Research Emory UniversityAssociate Director, Biostatistics | School of Medicine - Pediatrics, Innovation ResearchAtlanta, GeorgiaFull timeADDITIONAL JOB DETAILS: Serves as a senior biostatistical expert and collaborator for complex pediatric and clinical research projects, including study design, statistical analysis planning, sample size and power calculations, advanced data analysis, interpretation of findings, and preparation of statistical sections for grants, protocols, presentations, and manuscripts. PREFERRED QUALIFICATIONS: Deep applied expertise in classical and contemporary statistical methods relevant to pediatric and clinical research, such as generalized regression modeling, longitudinal and mixed-effects models, survival and competing risks analysis, trajectory and latent-variable modeling, data visualization, and other advanced analytic approaches.
Associate Director, Biostatistics | School of Medicine Pediatrics, Innovation Research Emory UniversityAssociate Director, Biostatistics | School of Medicine Pediatrics, Innovation ResearchAtlanta, GAADDITIONAL JOB DETAILS: Serves as a senior biostatistical expert and collaborator for complex pediatric and clinical research projects, including study design, statistical analysis planning, sample size and power calculations, advanced data analysis, interpretation of findings, and preparation of statistical sections for grants, protocols, presentations, and manuscripts. PREFERRED QUALIFICATIONS: Deep applied expertise in classical and contemporary statistical methods relevant to pediatric and clinical research, such as generalized regression modeling, longitudinal and mixed-effects models, survival and competing risks analysis, trajectory and latent-variable modeling, data visualization, and other advanced analytic approaches.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceGATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedGATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Assistant Scientist (Academic Research) - Emory College of Arts and Sciences Emory UniversityAssistant Scientist (Academic Research) - Emory College of Arts and SciencesAtlanta, GeorgiaFull timeADDITIONAL JOB DETAILS: The Ling Lab in the Department of Biology at Emory University is looking for a research scientist or postdoctoral fellow to study how transcription machinery dynamically searches for targets, binds chromatin, and regulates gene expression in living cells. Work may include building and validating yeast strains, performing imaging experiments, analyzing microscopy data, working closely with the PI, graduate students, and other lab members, and contributing to day-to-day lab organization and operations.
Assistant Scientist (Academic Research) Emory College of Arts and Sciences Emory UniversityAssistant Scientist (Academic Research) Emory College of Arts and SciencesAtlanta, GARemoteUnder minimal supervision, the Assistant Academic Research Scientist performs a wide range of highly technical and complex tasks necessary to advance basic and/or translational research programs. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD).
Clinical Research Nurse Alcanza Clinical ResearchClinical Research NurseDecatur, GARequesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team members; o Always practicing ALCOAC principles with all documentation; Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study; Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc. Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
RN Research Coordinator WellStar Health System IncRN Research CoordinatorGAThis includes responsibility for identifying potential study patients; ascertaining patient eligibility for clinical trials; coordinating, evaluating, and following patients in clinical trials; coordinating therapy initiation and continuation; taking call for issues related to clinical trials; completing and filing necessary forms with internal and external departments and agencies as necessary; and maintaining records for patients enrolled in clinical trials. Required Minimum Skills: Strong computer skills; good oral and written communication skills; excellent interpersonal and organization skills.