Medical Director, Sickle Cell Disease, Clinical Development Agios PharmaceuticalsMedical Director, Sickle Cell Disease, Clinical DevelopmentAtlanta, GA$221,600–$369,333 / yearThe current base salary range for this position is expected to be between $221,600 and $369,333 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Follow important developments and relevant trends in scientific literature and develop/maintain contracts with external experts to support understanding of the candidate drug effects and to gain strategic insights to the further development and placement of study and overall program.
NewRN Navigator Float Kaiser PermanenteRN Navigator FloatAtlanta, GA$47.37–$47.37Responsible for outreach to maintain a positive working relationship as appropriate with key customers (physicians, office staff, diagnostics, radiology staff, inpatient nurses, lab staff, primary care, palliative care, and all other specialty services needed). Work with quality staff, research team members, and other healthcare team partners to collect data, monitor trends, track outcomes, support and/or participate in research projects, and facilitate strategic planning processes related to patient care.
NewRN Navigator Endocrinology Diabetic Educator Kaiser PermanenteRN Navigator Endocrinology Diabetic EducatorJonesboro, GA$47.37–$47.37Responsible for outreach to maintain a positive working relationship as appropriate with key customers (physicians, office staff, diagnostics, radiology staff, inpatient nurses, lab staff, primary care, palliative care, and all other specialty services needed). Work with quality staff, research team members, and other healthcare team partners to collect data, monitor trends, track outcomes, support and/or participate in research projects, and facilitate strategic planning processes related to patient care.
Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLCClinical Research Associate (CRA) - Cardiovascular Medical DeviceMarietta, GARemoteContribute 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.
In-house Clinical Research Associate (CRA) - Cardiovascular Medical Device MiRus LLCIn-house Clinical Research Associate (CRA) - Cardiovascular Medical DeviceMarietta, GAContribute 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.
NewResearch Specialist- School of Medicine, Medical Oncology Emory Healthcare/Emory UniversityResearch Specialist- School of Medicine, Medical OncologyAtlanta, 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). + Performs related responsibilities as required by principal investigator MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field + OR equivalent combination of experience, education, and training.
Research Specialist School of Medicine, Medical Oncology Emory UniversityResearch Specialist School of Medicine, Medical OncologyAtlanta, 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). KEY RESPONSIBILITIES: Under general supervision, performs a variety of defined research and laboratory tests and experiments according to prescribed protocols and assigned schedules.
Research Specialist- School of Medicine, Medical Oncology Emory UniversityResearch Specialist- School of Medicine, Medical OncologyAtlanta, 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. KEY RESPONSIBILITIES: Under general supervision, performs a variety of defined research and laboratory tests and experiments according to prescribed protocols and assigned schedules.
Clinical Research Coordinator - Clinical Research CenExel IResearch LLCClinical Research Coordinator - Clinical ResearchSavannah, GA$25–$29 / hourPart timeResponsible 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. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Clinical Research RN -Research Infusion Nurse Coordinator Avery Partners, LLCClinical Research RN -Research Infusion Nurse CoordinatorAtlanta, GACompany Overview: Avery Partners is a leading healthcare staffing and consulting firm that specializes in providing top-notch professionals to healthcare organizations across the country. You will work closely with physicians, research staff, and patients to ensure the successful execution of research protocols and the delivery of high-quality patient care.
Clinical Research Coordinator - Clinical Research CenExelClinical Research Coordinator - Clinical ResearchSavannah, GeorgiaResponsible 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. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Clinical Research Assistant Adams ClinicalClinical Research AssistantHarlem, New YorkWorking under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
Clinical Research Coordinator II (Relocation Opportunity) Care AccessClinical Research Coordinator II (Relocation Opportunity)Dalton, 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 Assistant Care AccessClinical Research AssistantDalton, GA$19–$33 / hourWith 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 Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
Clinical Research Coordinator III Adams ClinicalClinical Research Coordinator IIIHarlem, New YorkOversee investigational product (IP) accountability across all assigned trials, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal; ensure compliance with protocol, regulatory requirements, and site SOPs, and provide guidance and oversight to CRCs and RAs supporting IP management. Serve as the primary operational lead for study start-up activities, including SIV and PSV readiness, document preparation, development of site workflows, staff training completion, and management of study supplies.
Float Clinical Research Coordinator II Fresenius Medical CareFloat Clinical Research Coordinator IIKennesaw, Georgia2 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.
NewRegional Travel, Clinical Research Coordinator Care AccessRegional Travel, Clinical Research CoordinatorDecatur, GA$75,000–$105,000 / 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 Quality Control Associate CenExel IResearch LLCClinical Research Quality Control AssociateDecatur, GAPart timeWorking closely with clinical operations, data management, and regulatory teams, the QC Associate reviews essential trial documents and clinical data to verify compliance with GCP (Good Clinical Practice), ICH guidelines, regulatory requirements, and internal SOPs. Performs quality control reviews of clinical trial documents (e.g., informed consent forms, case report forms, regulatory binders, monitoring visit reports) to ensure accuracy, completeness, and consistency.
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 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.
Oncology Research Data Specialist - Gwinnett Hub Northside Hospital IncOncology Research Data Specialist - Gwinnett HubLawrenceville, GAKNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION REQUIRED Associates Degree from an accredited college or university KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION PREFERRED Bachelor of Arts or Bachelor of Science degree from an accredited college or university in a data driven research - related field (such as allied health, biological sciences, chemistry, economics, mathematics, psychology, sociology, demography, geography, anthropology, statistics, data science). Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research.
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 Pharmacist CenExel IResearch LLCClinical Research PharmacistSavannah, GAPart timeThe Pharmacist shall coordinate, collaborate and provide expertise in support of clinical investigational drug trials; perform training responsibilities; provide accurate and efficient dispensing of medication; perform administrative responsibilities; maintain overall responsibility for pharmacy operations; perform cross functional duties as required. Must have in depth knowledge of FDA regulations, GCP, and ICH guidelines; Able to take a flexible approach to shifting priorities; Able to manage multiple projects and responsibilities; Motivated to work consistently in a fast paced and rapidly changing environment.
Clinical Research Assistant Care Access Research LLCClinical Research AssistantDalton, GA$19–$33 / hourWith 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 Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
Clinical Research Coordinator II Care Access Research LLCClinical Research Coordinator IIDalton, 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 II Adams ClinicalClinical Research Coordinator IIHarlem, New YorkMaintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs. This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.
NewRegional Travel, Clinical Research Coordinator Care Access Research LLCRegional Travel, Clinical Research CoordinatorDecatur, GARemote$75,000–$105,000 / 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.
NewClinical Research Nurse Denali HealthClinical Research NurseAtlanta, GAWe 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.
Oncology Research Data Specialist, Forsyth Northside Hospital Inc.Oncology Research Data Specialist, ForsythCumming, GeorgiaFull timeThe RDS works closely with the Clinical Research Nurses (CRN) and Clinical Research Coordinators (CRC) to complete all data-related tasks. If not Certified Clinical Research Professional (CCRP) at time of hire, must achieve professional certification through Society of Clinical Research Associates (SOCRA) by deadline assigned to specific work location.
Oncology Research Data Specialist, Canton Northside Hospital Inc.Oncology Research Data Specialist, CantonCanton, GeorgiaFull timeThe RDS works closely with the Clinical Research Nurses (CRN) and Clinical Research Coordinators (CRC) to complete all data-related tasks. If not Certified Clinical Research Professional (CCRP) at time of hire, must achieve professional certification through Society of Clinical Research Associates (SOCRA) by deadline assigned to specific work location.
Clinical Research Coordinator I Ora IncClinical Research Coordinator IAtlanta, GAPerform 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.
NewClinical Research Assistant, PRN Care AccessClinical Research Assistant, PRNAtlanta, GA$34–$44 / hourWith 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).
NewClinical Research Assistant, PRN (Registered Nurse) Care AccessClinical Research Assistant, PRN (Registered Nurse)Atlanta, GA$34–$44 / hourWith 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. As 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.
Principal Carelon Research Biostatistician Elevance HealthPrincipal Carelon Research BiostatisticianAtlanta, MassachusettsThis researcher partners with investigators, research sponsors, academic institutions, and cross-functional project teams to design studies, develop statistical methodologies, oversee analytical execution, and communicate scientific findings that advance externally funded clinical research programs. Experience designing clinical research studies, developing sample size calculations, statistical analysis plans, outcome measures, and advanced statistical methodologies including survival analysis, causal inference, and experimental design preferred.
Clinical Research & Data Coordinator Morehouse School of MedicineClinical Research & Data CoordinatorAtlanta, GAPOSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS: Community Engagement: Identify and coordinate meetings between study staff and influential community (healthcare, churches, health promotion organizations, etc.) authorities and stakeholders, including but not limited to clinic administrators, physicians, church leaders. Posting Number NONAC3731 Job Title Clinical Research & Data Coordinator Position Title Clinical Research & Data Coordinator Position Type Non-Faculty Number of vacancies 1 Salary Commensurate with experience Department Cancer Health Equity Institute Position Summary.
Research Coordinator Cardiovascular Associates of AmericaResearch CoordinatorCanton, GeorgiaThe Clinical Research Coordinator will be responsible for supporting the growth and development of the research program while collaborating with clinic staff on existing and new clinical trials. As a Clinical Research Coordinator, you will play a key role in coordinating and overseeing clinical trials and supporting site operations.
Experienced Clinical Research Associate Medpace Holdings IncExperienced Clinical Research AssociateAtlanta, GAWe leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Our European clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team, in the country of Georgia.
Physician, MD/DO - Clinical Research Headlands Research IncPhysician, MD/DO - Clinical ResearchAtlanta, GAAs a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Clinical Research Atlanta (CRA), located in Stockbridge, Georgia, is a leading multi-specialty research center with a long-standing reputation for excellence.
NewClinical Research Coordinator Actalent IncClinical Research CoordinatorDalton, GA$60,000–$90,000 / yearYou will participate in pre-study visits, monitoring visits, and investigator meetings, and help ensure that all study supplies, lab kits, medications, and specialized equipment are available and ready for use. This position combines direct patient coordination, meticulous documentation, and proactive recruitment activities to support high-quality, compliant research that expands access to health services and advances medical knowledge.
Clinical Research Coordinator, On-site, Lilburn, GA IQVIA Holdings IncClinical Research Coordinator, On-site, Lilburn, GALilburn, GA$36,600–$91,300 / yearJoin 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.
NewClinical Research Assistant, PRN Registered Nurse Care Access Research LLCClinical Research Assistant, PRN Registered NurseAtlanta, GA$34–$44 / hourWith 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. As 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.
NewClinical Research Assistant, PRN Care Access Research LLCClinical Research Assistant, PRNAtlanta, GA$34–$44 / hourWith 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 Nurse (RN) Manager - Atrium Health Navicent Trauma Services Advocate Aurora Health IncClinical Research Nurse (RN) Manager - Atrium Health Navicent Trauma ServicesMacon, GA$47.50–$71.25 / hourHeadquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. Atrium Health Navicent Medical Center is a nationally recognized academic medical center, nationally verified Level 1 Trauma Center, Magnet hospital for nursing, and serves a service area of 30 counties and a population of nearly 750,000 persons.
NewClinical Research Coordinator I-School of Medicine, Georgia CTSA Emory UniversityClinical Research Coordinator I-School of Medicine, Georgia CTSAAtlanta, 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.
NewClinical Research Coordinator I School of Medicine, Georgia CTSA Emory UniversityClinical Research Coordinator I School of Medicine, Georgia CTSAAtlanta, 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.
NewSenior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Atlanta, GeorgiaFor that reason, we treat our team members with the respect they deserve, and our numbers show it:We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Quality Control Associate CenExelClinical Research Quality Control AssociateDecatur, GeorgiaWorking closely with clinical operations, data management, and regulatory teams, the QC Associate reviews essential trial documents and clinical data to verify compliance with GCP (Good Clinical Practice), ICH guidelines, regulatory requirements, and internal SOPs. Performs quality control reviews of clinical trial documents (e.g., informed consent forms, case report forms, regulatory binders, monitoring visit reports) to ensure accuracy, completeness, and consistency.
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 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.
NewClinical Research Scientist (On Site) Atlanta ARTHRO-RESEARCH LLCClinical Research Scientist (On Site) AtlantaAtlanta, GAAt Ermi, we are building a clinically validated platform that is redefining how patients recover range of motion after injury and surgery. This is a founding-level R&D role where you will: Publish and present research that directly influences clinical adoption.