On-Site Clinical Trials Coordinator - Regulatory & Study Ops
HR Anew
Prime Clinical Research is seeking an experienced Study Coordinator to support the day-to-day execution of clinical trials while also assisting with regulatory documentation and compliance activities on-site. This role coordinates participant visits, supports study enrollment, maintains regulatory documentation, and ensures trials are conducted in accordance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. #J-18808-Ljbffr HR Anew
$135k - $145k
...largest early phase site network, fully... ...dedicated to oncology clinical research.... ...Access”to cutting edge trials throughout the United... ...a Director of Study Operations will lead... ...START standards, regulatory standards, and with... ...Clinical Research Coordinator, Data Coordinator...WebsiteRegulatoryLocal areaWorldwideFlexible hours- ...for all aspects of assigned clinical trials. Lead the Clinical Trial Team... ...clinical trial teams for studies of medium to high complexity... ...team to select countries and sites.Ensure investigational product... ...of clinical sections of regulatory documents like Investigators...WebsiteRegulatoryContract workWork at officeImmediate startRemote work
- ...implements and executes client s phase I III clinical trials at their assigned sites• Ensures compliance with regulations, guidelines and policies for studies implemented at their assigned sites.... ...in timelines appropriate to the regulatory and protocol requirements.• Develop...WebsiteRegulatoryContract workWork at officeImmediate startHome office
- ...defining and leading the clinical development strategy... ...early-phase clinical trials. This role requires a... ...early-phase clinical studies, providing medical oversight... ...and submission of key regulatory documents. The role... ..., and trial sites, as well as collaborating...WebsiteRegulatory
$45k - $55k
...Clinical Research Coordinator Prime Clinical Research ( Location: On-Site Employment Type: Full-Time Department: Clinical... ...execution of clinical trials while also assisting with regulatory documentation and... ...participant visits, supports study enrollment, maintains...WebsiteRegulatoryFull timeContract work- Re.Cognition Health US in Fort Worth, TX is recruiting for a Clinical Trials/PC Coordinator to manage clinical trials operations, patient scheduling, and data integrity. The role ensures safety, regulatory compliance, and efficient patient flow across private practice...RegulatoryPrivate practice
$71.9k - $169.3k
...a minimum of 1 year of on-site monitoring and will also consider... ...are seeking a dedicated Clinical Research Associate (CRA) to... ...execution of clinical trials. In this position, you will... ...to ensure compliance with study protocols, regulatory requirements, and sponsor expectations...WebsiteRegulatoryFull timePart timeImmediate startWorldwide- ...The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process.... ...to assess protocol and regulatory compliance and manages... ...specialist, ensuring that the trial is conducted in... ...as required. Ensures study systems are updated per...WebsiteRegulatoryFull timePart timeWork at officeRemote workFlexible hours
- ...largest early phase site network, fully... ...dedicated to oncology clinical research.... ...areseekinga Data Coordinator. This role will collect... ...investigational drug studies. Schedule: Monday... ...communicate to the Regulatory Affairs staff so... ...START START clinical trial sites have...WebsiteRegulatoryWork at officeLocal areaWorldwideMonday to FridayFlexible hours
- ...largest early phase site network, fully... ...dedicated to oncology clinical research.... ...Access”to cutting edge trials throughout the United... ...Clinical Research Coordinator . The Clinical... ...adhering to protocols, regulatory requirements, and... ...basis with Study Sponsor’s, CRO’s,...WebsiteRegulatoryCurrently hiringWork at officeLocal areaWorldwideMonday to FridayFlexible hours
- ...Research in Fort Worth, Texas is seeking a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will ensure protocol adherence, data integrity... .... Responsibilities include monitoring studies per GCP, training staff, assisting with...
$65k - $70k
...highest standards of operational delivery of the Clinical Trials for which the post holder is appointed to co-ordinate... ...within the time frames dictated for each study and GCP Private Practice Support: Coordinate all patient visits for monoclonal antibody infusions...Private practiceWork at officeWorldwide- IntelliSource is seeking an Asset Protection and Safety Coordinator to safeguard our facility, health and safety programs, and regulatory compliance within a fast-paced distribution environment. You will partner with site leadership to reduce risk, support incident response...WebsiteRegulatoryContract work
$87.2k - $145.3k
...minimum of 1.5 years of on-site oncology monitoring... ...contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International... ...protocol and related study training to assigned sites... ...available for filing in the Trial Master File (TMF) and verify...WebsiteRegulatoryFull timePart timeLocal areaImmediate startWorldwide- ...according to Parkland, stat, and regulatory standards. Minimum... ...catheterization, peripheral vascular studies and/or electrophysiology... ...and resource to medical and clinical staff as needed. Assists with... ...in Universal Protocol and site marking identification (when...WebsiteRegulatoryRelief
- ...spans basic "bench-top" science, clinical research, community-based research and clinical trials. Our translational approach is... ...quality assurance processes, regulatory compliance, operational readiness... ...Monday - Friday 8a-5p On Site Driving University Vehicle...WebsiteRegulatoryTemporary workLocal areaMonday to Friday
- ...spans basic "bench-top" science, clinical research, community-based research and clinical trials. Our translational approach is... ...quality assurance processes, regulatory compliance, operational readiness... ...Monday - Friday 8a-5p On Site Driving University Vehicle No Security...WebsiteRegulatoryTemporary workLocal areaMonday to Friday
- ...therapy, physician assistant studies, nutrition, lifestyle health... ...interprofessional collaboration, clinical practice, education, and... ...practice expectations, including site placement and... ...settings. Knowledge of legal, regulatory, ethical, and governance frameworks...WebsiteRegulatoryFull time
- ...Care System seeks a Research Nurse Coordinator to implement designated trials and provide skilled nursing care... ...research coordination, guided by regulatory standards, sponsor requirements, and... ...strong customer relations, and sound clinical judgment in a university-...Regulatory
- Re:Cognition Health in Fort Worth is seeking a Clinical Trials Coordinator to support the Regional Manager in delivering trials in accordance with GCP and FDA requirements. You will ensure patient care, coordinate visits, manage records, and maintain center operations to...
- ...Clinical Risk Coordinator Location: Rosedale Office Building Department: Risk Management Shift: First Shift (United States of America... ...risk-related initiatives, and ensures compliance with all regulatory standards. Qualifications ~ Bachelor's degree in Nursing...RegulatoryWork at officeShift workDay shift
$165.25k - $236k
...the limits off living. The Director of Clinical Data & AI is the global functional leader... ...interoperable, and fit-for-purpose for regulatory, scientific, and operational decision-making... ...and geographiesPartner with Clinical Study Management, Clinical Strategy, Regulatory...WebsiteRegulatoryFull timeFlexible hours- ...Center for Cancer Research is seeking a Director of Study Operations to lead research operations, oversee Clinical Research Coordinators, Data Coordinators, and Medical Records to ensure quality patient care and regulatory compliance. This role provides direction across...RegulatoryRemote job
$235.2k - $341.2k
...ideal candidate understands the unique operational, financial, regulatory, and resident experience considerations involved in... ...and project performance. Lead master planning, feasibility studies, site selection, entitlement, permitting, and zoning activities....WebsiteRegulatoryFull timeContract workFor contractors- ...levees. You will be responsible for leading site inspections and the analysis, design, and... ...through deliveryDirect and supervise studies, investigations, and designs to ensure continuity... ...with clients, client staff, regulatory agencies, and project teamsEvaluate design...WebsiteRegulatoryFull timeContract workLocal areaRemote workFlexible hours
- ...secure employment in their chosen field of study. Key aspects of this role include:... ...opportunities. Ensuring compliance with all regulatory standards, including state, federal, and... ..., recruiting externship and placement sites, marketing to the medical community, and...WebsiteRegulatory
- ...end programming, master planning, concept studies, and FEED package development for design-... ...engineering solutions, incorporating site selection, building systems, operational... ...industry standards, best practices, and regulatory requirements.Lead client requests for proposals...WebsiteRegulatoryFull timeLocal areaFlexible hours
- ...Position Overview:Ensure the site Environmental programs are implemented... ...inventories, and ongoing regulatory dialogue with MDAQMD, CARB,... ...under 43 CFR 3809, in coordination with the Needles Field Office... ...EISs, and supporting technical studies, for mine expansion and infrastructure...WebsiteRegulatoryPermanent employmentWork at officeLocal area
- ...team, you will lead traffic studies and transportation analyses for... ...roadway operations to assess site access, circulation, traffic... ...project development, client coordination, and agency discussions.Apply... ...judgment, industry standards, and regulatory requirements while managing...WebsiteRegulatoryFull timeFlexible hours
- ...We are seeking transmission routing and siting professionals to support HDR’s expanding... ...testimony and technical documentation including studies to present defensible line route and... ...in routing, siting and supporting regulatory approvals for electric facilities. Expert...WebsiteRegulatoryWork at office
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