Clinical Research RN CenExel IResearch LLCClinical Research RNDecatur, GAPart timeul>Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Clinical Research Coordinator III - Psychiatry Washington University in St LouisClinical Research Coordinator III - PsychiatryForest Park, GeorgiaClinical Research Management, Clinical Study Protocols, Database Management, Data Entry, Detail-Oriented, Freezerworks (Software), Ordering Supplies, Organizing, Participant Recruiting, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Team Supervision, Written CommunicationGrade. This person will oversee and coordinate complex or multi-site clinical research studies, serve as a resource to provide comprehensive information to clinical research staff, promote smooth clinical operations, prepare regulatory compliance documents, coordinate interaction with other departments, and supervise clinical research coordinators and staff.Job Description.
Float Clinical Research Coordinator II Fresenius Medical CareFloat Clinical Research Coordinator IIKennesaw, Georgiaul>2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures. Provides relevant information regarding the projected regional costs of treatments, projected enrollment capabilities, anticipated risks/benefits at specific study sites, logistical impediments, etc. for use in study contract and budget negotiations.
Clinical Research Coordinator CenExel IResearch LLCClinical Research CoordinatorDecatur, GAPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Assistant Director, Clinical Research Staff Winship Cancer Institute Emory UniversityAssistant Director, Clinical Research Staff Winship Cancer InstituteAtlanta, GACancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Research Laboratory Technician CenExel IResearch LLCClinical Research Laboratory TechnicianDecatur, GAPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Obtains samples per protocol, performs select diagnostic test or limited high complexity testing and documents process in source documents.
Clinical Research Assistant, PRN Care AccessClinical Research Assistant, PRNAtlanta, GA$34–$44 / hourp>With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse) Care AccessClinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse)Atlanta, GA$19–$44 / hourp>With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Assistant Director, Clinical Research Staff- Winship Cancer Institute Emory UniversityAssistant Director, Clinical Research Staff- Winship Cancer InstituteAtlanta, GeorgiaCancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
In-house Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLCIn-house Clinical Research Associate (CRA) - Cardiovascular Medical DeviceMarietta, GAp>Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents. The role will assist with the management of cardiovascular clinical studies for MiRus products, with a focus on meeting critical timelines, developing high-quality documentation, and ensuring accurate data collection.
Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLCClinical Research Associate (CRA) - Cardiovascular Medical DeviceMarietta, GARemotep>Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents. Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager.
Senior Clinical Research Associate - Cardio - East Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Cardio - East Coast - RemoteGARemote$97,000–$193,000 / yearli>Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - CNS/Psychiatry - East Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - East Coast - RemoteGARemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Clinical Research Assistant/ Certified Medical Assistant Alcanza Clinical Research LLCClinical Research Assistant/ Certified Medical AssistantWoodstock, GAResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; 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; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Clinical Research RN CenExelClinical Research RNDecatur, Georgiaul>Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Clinical Trial Manager - Cardiovascular Medical Device MiRus LLCClinical Trial Manager - Cardiovascular Medical DeviceMarietta, GAp>Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents. Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager.
Clinical Research Assistant, PRN Care Access Research LLCClinical Research Assistant, PRNAtlanta, GA$19–$44 / hourp>Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA). As a Clinical Research Assistant, PRN, you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.
Clinical Research Assistant, PRN Registered Nurse Care Access Research LLCClinical Research Assistant, PRN Registered NurseAtlanta, GA$19–$44 / hourAs a Clinical Research Assistant, PRN (Registered Nurse) you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life. Walking - 20% Standing - 40% Sitting - 30% Lifting (up to 25 lbs., over 25lbs, and overhead) - 10% Driving - <10% Exposure to bloodborne pathogens - 50% (variable by station supporting).
Clinical Research Coordinator CenExelClinical Research CoordinatorDecatur, GeorgiaRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Clinical Research Coordinator II Care Access Research LLCClinical Research Coordinator IIDecatur, GA$60,000–$90,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorDecatur, GAResponsibilities may include but are not limited to: • Screening of patients for study enrollment • Patient consents • Patient follow-up visits • Documenting in source clinic charts • Entering data in EDC and answering 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 • Requesting 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 • Filing SAE • Deviation reports to Sponsor and IRB as needed • Documenting and reporting adverse events • Reporting non-compliance to appropriate staff in timely manner • Maintaining positive and effective communication with clients and team members • Always practicing ALCOA principles with all documentation • May assist with study recruitment, patient enrollment, and tracking as needed • Maintaining confidentiality of patients, customers, and company information • Performing all other duties as requested or assigned • Complete all needed activities for study start-up including completing required training, uploading printing certificates to file in ISF, etc. • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently 40 wpm • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc.
Clinical Research Laboratory Technician CenExelClinical Research Laboratory TechnicianDecatur, GeorgiaRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Obtains samples per protocol, performs select diagnostic test or limited high complexity testing and documents process in source documents.
Clinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorDecatur, GAli>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; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: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; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Lead Clinical Data Manager (Remote) IQVIA Holdings IncLead Clinical Data Manager (Remote)Atlanta, GARemoteYour previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials.
Clinical Research Nurse II | School of Medicine Pediatrics, Infectious Disease Emory UniversityClinical Research Nurse II | School of Medicine Pediatrics, Infectious DiseaseAtlanta, 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). Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.
Clinical Research Nurse II | School of Medicine - Pediatrics, Infectious Disease Emory UniversityClinical Research Nurse II | School of Medicine - Pediatrics, Infectious DiseaseAtlanta, 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. Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.
Clinical Research and Data Coordinator Morehouse School of MedicineClinical Research and Data CoordinatorAtlanta, GAThis pivotal role is responsible for facilitating the timely and accurate data analysis of participants to appropriate clinical trials, with an emphasis on leveraging electronic health records (EHRs) for participant identification and data management, formulation, and preparation of official institutional information to internal and/or external parties. Formulate and prepare official institutional information to internal and/or external queries and requests for institutional data and statistics on a wide range of issues, including university information, student characteristics (enrollment, degrees, retention, etc.), faculty characteristics, employment/benefits, financial information, and projections.
Sr. Clinical Trials Manager Agilent Technologies IncSr. Clinical Trials ManagerGAMonitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.
Clinical Trials Manager - School of Medicine, Emergency Medicine Emory UniversityClinical Trials Manager - School of Medicine, Emergency MedicineAtlanta, 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. ADDITIONAL JOB DETAILS: Provides leadership and oversight of significant clinical research project(s) with an emphasis on managing, evaluating and training research staff.
Clinical Research Coordinator IV Winship Cancer Institute Emory UniversityClinical Research Coordinator IV Winship Cancer InstituteAtlanta, GACancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Research Coordinator IV School of Medicine Orthopaedics Emory UniversityClinical Research Coordinator IV School of Medicine OrthopaedicsAtlanta, GARemoteli>Or master''s degree, MD or PhD in a scientific, health related, or business administration program and two years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator IV - School of Medicine Orthopaedics Emory UniversityClinical Research Coordinator IV - School of Medicine OrthopaedicsAtlanta, GeorgiaRemoteli>Or master's degree, MD or PhD in a scientific, health related, or business administration program and two years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. Discover 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.
Clinical Research Coordinator IV- Winship Cancer Institute Emory UniversityClinical Research Coordinator IV- Winship Cancer InstituteAtlanta, Georgiap style="margin:0px">Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer. Cancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer.
Clinical Research Specialist Diagnostica Stago IncClinical Research SpecialistGACollaborates on development of study protocols, data collection tools, lab manuals, case reports, and databases with French counterparts to help conduct and support clinical trials in the US regarding support new Hematology and Hemostasis products and parts. Minimum five years hospital experience in Hematology and Coagulation preferably experienced with validations, correlations and training lab staff on new laboratory instrumentation.
Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide Headlands Research IncClinical Research Coordinator I/II/III Opportunities - Multiple Locations NationwideAtlanta, GA$45,000–$100,000 / yearp>This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
Clinical Research Coordinator I Ora IncClinical Research Coordinator IAtlanta, GAp>Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
Clinical Research Coordinator III Winship Cancer Institute Emory UniversityClinical Research Coordinator III Winship Cancer InstituteAtlanta, GAOr two years of college in a scientific, health related or business administration program and five years of clinical research experience Or licensed as a Practical Nurse (LPN) and four years of clinical research experience Or bachelor''s degree in a scientific, health related or business administration program and three years clinical research experience Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. Description About Winship Cancer Institute of Emory University Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Research Coordinator III- Winship Cancer Institute Emory UniversityClinical Research Coordinator III- Winship Cancer InstituteAtlanta, GeorgiaCancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Trials Regulatory Specialist III Winship Cancer Institute Emory UniversityClinical Trials Regulatory Specialist III Winship Cancer InstituteAtlanta, GACancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Research Coordinator, On-site, Lilburn, GA IQVIAClinical Research Coordinator, On-site, Lilburn, GALilburn, GeorgiaJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits.
Clinical Research Coordinator III School of Medicine, Radiation Oncology Emory UniversityClinical Research Coordinator III School of Medicine, Radiation OncologyAtlanta, GAOr master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III School of Medicine Neurology Emory UniversityClinical Research Coordinator III School of Medicine NeurologyAtlanta, GARemoteOr master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator II Winship Cancer Institute Emory UniversityClinical Research Coordinator II Winship Cancer InstituteAtlanta, GACancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Clinical Research Coordinator III School of Medicine, Infectious Diseases Emory UniversityClinical Research Coordinator III School of Medicine, Infectious DiseasesAtlanta, GARemoteli>Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III School of Medicine Psychiatry Emory UniversityClinical Research Coordinator III School of Medicine PsychiatryAtlanta, GARemoteli>Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III School of Medicine, Obstetrics and Gynecology Oncology Emory UniversityClinical Research Coordinator III School of Medicine, Obstetrics and Gynecology OncologyAtlanta, GARemoteli>Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III SOM, Infectious Diseases (Hope Clinic) Emory UniversityClinical Research Coordinator III SOM, Infectious Diseases (Hope Clinic)Decatur, GARemoteli>Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III Georgia CTSA Emory UniversityClinical Research Coordinator III Georgia CTSAAtlanta, GAOr two years of college in a scientific, health related or business administration program and five years of clinical research experience Or licensed as a Practical Nurse (LPN) and four years of clinical research experience Or bachelor''s degree in a scientific, health related or business administration program and three years clinical research experience Or master''s degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. 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 Coordinator III School of Medicine, Surgery Emory UniversityClinical Research Coordinator III School of Medicine, SurgeryAtlanta, 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). Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future.
NewClinical Research Coordinator II- Winship Cancer Institute Emory UniversityClinical Research Coordinator II- Winship Cancer InstituteAtlanta, Georgiap style="margin:0px">Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer. Cancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer.