Clinical Research Coordinator II School of Medicine Neurology Emory UniversityClinical Research Coordinator II School of Medicine NeurologyAtlanta, GARemoteThis position will support an NIH National Institute on Aging (NIA)-funded R01 study, "Improving Residual Sleepiness and Inflammation in Older Adults with OSA: A Randomized Controlled Trial of Citicoline," led by Principal Investigator Dr. Victoria Pak in collaboration with a multidisciplinary team of investigators, including Co-Investigator Dr. Lynn Marie Trotti, Director of the Emory Sleep Center. 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).
Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)GARemote$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 Coordinator/Nurse Alcanza Clinical Research LLCClinical Research Coordinator/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.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorAtlanta, GA$22–$25 / hourThis contract role focuses on patient-facing coordination, data entry, and logistical support for the current research team, with the possibility of supporting additional studies depending on performance and future needs. The environment includes active clinical settings such as hospitals and urgent care centers, where staff regularly use tablets, electronic data capture systems, and other study technologies during patient visits.
Research NP/PA School of Medicine, Infectious Diseases Emory UniversityResearch NP/PA School of Medicine, Infectious DiseasesAtlanta, GARemoteCurrently licensed as an advanced practice nurse in the state of Georgia by the Georgia Board of Nursing and certified as a Nurse Practitioner by the American Nurses Credentialing Center (ANCC) or equivalent body or Certified as a Physician''s Assistant by the National Commission on Certification of Physician Assistants (NCCPA). KEY RESPONSIBILITIES: Research Nurse Practitioner (NP) or Physician Assistant (PA) routinely applies medical knowledge and experience to direct the clinical course of research participants in clinical trials, assures study participant safety, and manages clinical research protocols and procedures.
Biology Student Research Assistant - Federal Work Study University of North GeorgiaBiology Student Research Assistant - Federal Work StudyGainesville, GAThe University of North Georgia, a regional multi-campus institution and premier senior military college, provides a culture of academic excellence in a student-focused environment that includes quality education, service, research, and creativity. Offers of employment are contingent upon completion of a background investigation including a criminal background check demonstrating your eligibility for employment with the University of North Georgia, as determined by University of North Georgia in its sole discretion, confirmation of the credentials and employment history reflected in your application materials and, if applicable, a satisfactory credit check.
Clinical Research Physician - Internal Medicine Alcanza Clinical Research LLCClinical Research Physician - Internal MedicineWoodstock, GAEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Call Center Patient Recruiter (Clinical Research) CenExelCall Center Patient Recruiter (Clinical Research)Decatur, GeorgiaEach of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Clinical Research Coordinator I- School of Medicine, Obstetrics and Gynecology Emory UniversityClinical Research Coordinator I- School of Medicine, Obstetrics and GynecologyAtlanta, GeorgiaFull timeCoordinators are expected to demonstrate initiative and accountability for study-related responsibilities, maintain a high level of productivity and attention to detail, and communicate proactively with study leadership regarding project progress and scheduling needs. 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 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.
Clinical Research Coordinator I School of Medicine, Obstetrics and Gynecology Emory UniversityClinical Research Coordinator I School of Medicine, Obstetrics and GynecologyAtlanta, GARemoteCoordinators are expected to demonstrate initiative and accountability for study-related responsibilities, maintain a high level of productivity and attention to detail, and communicate proactively with study leadership regarding project progress and scheduling needs. 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 Associate 1 Allen SpoldenClinical Research Associate 1Atlanta, GeorgiaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Coordinator IV- School of Medicine, Emergency Medicine Emory UniversityClinical Research Coordinator IV- School of Medicine, Emergency MedicineAtlanta, GeorgiaFull timeOr 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 Physician - Internal Medicine Alcanza Clinical ResearchClinical Research Physician - Internal MedicineWoodstock, GAEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Nurse II | School of Medicine - Pediatrics, Infectious Disease Emory UniversityClinical Research Nurse II | School of Medicine - Pediatrics, Infectious DiseaseAtlanta, 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. Performs patient evaluations, administers medications and research instruments and provides nursing support to perform specialized diagnostic, therapeutic and surgical procedures.
Clinical Research Physician - Cardiologist (Part time) Alcanza Clinical Research LLCClinical Research Physician - Cardiologist (Part time)Decatur, GAEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Data Coordinator I - School of Medicine, Urology Emory UniversityClinical Research Data Coordinator I - School of Medicine, UrologyAtlanta, GeorgiaFull timeReviews information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract data for all assigned research protocols including but not limited to industry, cooperative group, and investigator-initiated studies. This role collaborates with the clinical, informatics, quality monitors, and/or regulatory teams to document and report study patient enrollment, treatment, and follow-up information into databases as specified by research protocols.
Clinical Research Nurse Denali HealthClinical Research NurseAtlanta, GeorgiaWe conduct Phase I-IV clinical trials across multiple therapeutic areas, including neurology, psychiatry, wound care, and other specialty areas. Note: This is a part-time position that requires working one week per month on-site according to the following schedule: Tuesday- Friday: Night shift.
NewSenior Clinical Research Associate IRESenior Clinical Research AssociateAtlanta, GeorgiaThe ideal candidate will have cardiovascular medical device monitoring experience- however, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience will be considered. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Teaching/Research Assistant- only for Mercer DPS students Mercer UniversityTeaching/Research Assistant- only for Mercer DPS studentsAtlanta, GeorgiaResponsibilities include: Teaching responsibility for laboratories or discussion sessions; a limited number of didactic lectures per semester based on discipline; assignment to a professor for a semester to assist with classroom activities such as grading, recording, proctoring, preparation of course materials, etc. or assistance with other Departmental needs such as care and maintenance of animals and the animal facility, analytical instrumentation, or Department equipment and facilities. • Planning studies and organizing supplies • Conducting Franz cell skin transport studies • Running assay for drug or cosmetic molecule • Data analysis • Writing Reports • Student may work up to 20 hours per week in accordance with student employment policies.