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The Clinical Research Coordinator supports a clinical research site, performing administrative and clinical tasks to ensure the smooth execution of clinical trials.
This clinical research nurse position supports the development of innovative new medicines by working on early phase and "first in human" trials. The role involves administering novel treatments to volunteer participants and monitoring their health status around the clock to ensure safety and…
Coordinating clinical trials and supporting patients throughout their participation is the core of this role. The Clinical Research Coordinator ensures all aspects of assigned study protocols are maintained in accordance with Good Clinical Practice, standard operating procedures…
This position within the Pediatrics Clinical Research Unit (PCRU) assists investigators as a coordinator of complex clinical research studies.
This home-based opportunity is for clinical research professionals with at least two years of Clinical Research Coordinator experience to become Clinical Research Associates (CRA) with Medpace.
This role involves overseeing and managing clinical operations at a research site, ensuring compliance with study protocols and regulatory guidelines.
This senior role is responsible for managing clinical trial sites, ensuring data quality, and overseeing the timely submission of study data and safety reports.
This role involves the execution and oversight of local operational clinical trial activities, ensuring compliance with ICH GCP and country regulations.
Leading outpatient dialysis care for patients with end-stage renal disease is the core of this Clinical Coordinator role. You will oversee treatment, guide clinical staff, and ensure the highest standards of care and safety.
This Clinical Research Coordinator B role involves a variety of tasks related to clinical studies, from conducting in-home and on-site visits to managing regulatory submissions and providing administrative support.
Coordinating participant visits, collecting data, and ensuring regulatory compliance are the core responsibilities of this field-based clinical research role.
The Clinical Research Coordinator will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.
Coordinating the administrative and logistical implementation of clinical research protocols is the core of this role, ensuring adherence to study guidelines and providing regulatory support.
This per diem/PRN position is for a Certified Mobile Research Nurse responsible for conducting mobile visits for study participants. The role involves setting appointments, performing clinical skills, and collaborating with project managers and site personnel to ensure accurate documentation.
Coordinating programs within the Research Department, this role provides administrative, logistical, communications, and programmatic support across various initiatives.
Designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies are the core functions of this Clinical Research Associate role.
This role involves supporting, facilitating, and coordinating the daily activities of clinical trials, playing a critical part in their execution.
This nursing role involves coordinating and conducting clinical trials under the guidance of a Principal Investigator and Manager/Director. The work adheres to good clinical practice standards and FDA regulations.
This clinical research coordinator role supports studies focused on diagnosing acute kidney injury in critically ill patients and those undergoing open heart surgery.
This entry-level human subjects researcher position involves conducting and assisting in clinical research studies within the psychiatry department.
This night-shift post on the cardiac ward pairs patient care with mentoring new nurses. The Clinical Research Coordinator II is responsible for the day-to-day coordination of interventional Phase I-III clinical trials and observational Cancer Control studies.
This night-shift post on the cardiac ward pairs patient care with mentoring new nurses. The Clinical Nurse Coordinator (CNC) delivers high-quality, patient-centered care and coordinates all functions in the unit.
Caring for patients and compiling data for clinical trials is the core of this role, which operates under limited supervision. The coordinator oversees daily trial activities in line with Good Clinical Research Practice, performing various research tasks, managing databases, and…
This night-shift post on the cardiac ward pairs patient care with mentoring new nurses. This role manages multiple clinical trial protocols, coordinates their execution and follow-up, and performs accurate documentation.
This Clinical Research Coordinator I position coordinates patient care in compliance with local, state, and federal guidelines and regulations through IRB approved protocol requirements.
This clinical research coordinator role involves performing the day-to-day administrative activities of clinical research trials and supporting the team to achieve program goals.
Managing a team of Clinical Research Associates (CRAs) and ensuring strong monitoring in clinical trials is the core of this role. The manager will ensure excellent study and site performance with strict adherence to local regulations, company SOPs, and ICH GCP.
This role supports clinical trials for new drugs and regenerative medicine at medical institutions. It involves managing subject schedules, providing care, creating reports, and assisting with informed consent explanations.
This onsite role involves ensuring the safety of volunteers, promoting Accellacare's mission, and striving to meet and exceed study priorities. The Clinical Research Coordinator 1 is responsible for recruiting and promoting services to suitable participants and sponsor representatives, as well as…
This temporary role involves overseeing and facilitating complex clinical trials in population and precision health, ensuring compliance with federal and institutional regulations.
This accounting coordinator role supports the financial transactions of clinical research activity at Dana-Farber Cancer Institute. The coordinator is responsible for creating accounts and managing accounts receivable, handling basic issues and referring complex ones to senior staff.
Clinical Research Coordinator II is a developmental position supporting the Principal Investigator in clinical trials by implementing and coordinating research, including administrative procedures, at Moffitt Cancer Center.
Working independently on progressively more complex projects within the Department of Orthopaedic Surgery, the Clinical Research Coordinator 2 (CRC2) conducts clinical research.
Coordinating and performing daily clinical research activities for sponsor-initiated trials in the Department of Psychiatry is the core of this role. The coordinator will recruit, interview, and enroll patients, ensuring compliance with regulatory and sponsor requirements throughout the consent…
This role assists with various activities related to human subject research within the Biomarker Exploration and Aging in Cancer and Health Equity (BEACH) lab. It involves gaining knowledge of clinical research procedures and protocols, maintaining logs, and assisting with data entry.
This Clinical Research Associate role focuses on leading performance and compliance for assigned protocols and sites within the South East, serving as the primary site contact throughout all phases of clinical studies.
Pediatric Clinical Research Nurses coordinate and implement pediatric clinical research protocols, collect and analyze clinical data, and ensure regulatory and ethical compliance.
This senior clinical research associate role involves monitoring clinical research studies to ensure they are conducted according to accepted clinical practices. It suits a professional with a drug development mindset who can navigate complexity and accelerate progress in a fast-paced environment.
The Clinical Coordinator plays a crucial role in ensuring the seamless coordination of patient care, assisting with all clinical needs for patients. This position involves proficient chart preparation, communication, scheduling of patient visits, appropriate utilization and logging of chronic care…
Joining the Clinical Decision Unit (CDU) at Chippenham Hospital, the Clinical Nurse Coordinator ensures and delivers high-quality, patient-centered care and coordinates all unit functions during their designated shift.
This night-shift post on the cardiac ward pairs patient care with mentoring new nurses. As a Clinical Support Coordinator, you will be a trusted clinical mentor who helps new graduate nurses and nurses moving into new specialties understand their roles, grow their clinical skills, and deliver safe…
This Clinical Research Coordinator (CRC) position provides study coordination for multiple clinical research studies, ranging from moderate to complex.
This full-time Clinical Research Coordinator I position supports clinical research studies within Pediatric Neurology Research. The role involves participant recruitment, data collection and entry, documentation, and communication with sponsors, ensuring adherence to study protocols and policies.
This opportunity is for experienced clinical research associates to help train a leading foundational AI lab's latest language model. The role involves creating, evaluating, and refining AI-generated professional documents, spreadsheets, and slide decks for core clinical workflows.
This Clinical Research Coordinator II position coordinates the day-to-day activities of research protocols, assessing and determining patient qualifications for research studies.
This experienced clinical research professional provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols.
This full-time Clinical Research Coordinator II (CRC II) role involves independently managing and overseeing the implementation and day-to-day conduct of clinical trials.
Coordinating and managing clinical research studies from participant recruitment to study closeout is the core of this role. The Clinical Research Coordinator ensures regulatory compliance, accurate data collection, and participant safety throughout the research process.
The Clinical Research Coordinator works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. This role involves patient screening, consents, follow-up visits, and documentation, ensuring all activities adhere to regulatory standards.
This role supports startup workflows, feasibility assessments, and budget coordination across sponsors, CROs, and study teams. It suits a specialist who can manage documents, review intake submissions, and ensure Epic RSH setup aligns with protocol requirements while tracking milestones in CTMS.