On-Site Cardiology Clinical Research Assistant
University of North Carolina at Chapel Hill
The University of North Carolina at Chapel Hill is seeking a Temporary Clinical Research Assistant to support Cardiology trials on-site in North Carolina. The role coordinates administrative and regulatory tasks, recruits and consents participants, and ensures accurate tracking of visits and payments. Minimum education is a bachelor’s degree with experience in clinical research and IRB processes. This on-site position offers a 40-hour work week and a start date around 10/01/2026, with a #J-18808-Ljbffr The University of North Carolina at Chapel Hill
$19 - $21 per hour
...Information Department: Medicine - Cardiology - 411405 Career Area: Research Professionals Posting Open Date... ...Staff (SHRA) Position Title: Clinical Research Assistant Position Number: 20068066... ...consenting patients, attending off-site study meetings as required, scheduling...WebsiteHourly payFull timeTemporary workPart timeLive inWork at officeLocal areaMonday to FridayFlexible hours- ...quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an... ...monitoring, and closeout visits at research sites in compliance with the approved... ...therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous...WebsiteContract workWork at officeRemote workWork from home
- ...quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an... ...monitoring, and closeout visits at research sites in compliance with the approved... ...therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous...WebsiteContract workWork at officeRemote workWork from homeHome officeFlexible hours
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- ProPharma Group is seeking a Research Assistant to support remote site activities across assigned projects. The role emphasizes day-to-day site communications... ..., pre-screening, data-entry, and monitoring of clinical databases. You will maintain IRB/FDA-compliant...WebsiteRemote jobFlexible hours
- ...domain expertise in regulatory sciences, clinical research solutions, quality & compliance,... ...to clinical trial execution, including assisting with the development, formatting, review... ...with the development and distribution of site binders and study materials, as requested...WebsiteFull timeWork at officeRemote work
- ...Experienced Clinical Research Associate II -Sponsored Syneos Health® is a leading fully integrated biopharmaceutical solutions organization... ...everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site...WebsiteInterim roleLocal areaImmediate startRemote work
- Worldwide Clinical Trials is seeking an In-house Clinical Research Associate II to manage sites per GCPs and SOPs. You will support CTMs and field CRAs while mentoring in-house staff, ensuring timely deliverables across trials. The role requires at least two years of clinical...WebsiteWorldwide
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- ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Study Specialist for a hybrid role... ...You will review study documents, maintain manuals, and track site activation and enrollment while communicating with sites and...Website
- ProPharma is seeking a Clinical Project Specialist to provide administrative and project management support for assigned clinical studies... ...timely execution. The role involves document development, tracking, site materials, and study trackers using CTMS, eTMF, and other...Website
- Emerald Clinical Trials is building a pipeline of Clinical Research Associates across the United States as we prepare for continued growth and new study awards. Join... ...renal, cardiometabolic, oncology studies, with on-site monitoring, site relationship building, and...WebsiteRemote job
- Worldwide Clinical Trials in the United States seeks an In-house Clinical Research Associate II to manage sites and ensure compliance with GCPs and SOPs. You will support CTMs and field CRAs and mentor junior staff. Responsibilities include site feasibility, TMF quality...WebsiteWorldwide
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- ...Clinical Research Associate For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise... ...and associated monitoring activities for assigned clinical sites both in person, and remote. This includes evaluation, site...WebsiteInterim roleWork at officeLocal areaRemote work
$97k - $193k
What Clinical Operations Does At Worldwide At Worldwide Clinical Trials, we invite you to embark on a rewarding... ..., and in-house CRAs for projects with heavy site management needs. Our commitment to advancing clinical research is nurtured with clear career paths leading to...WebsiteRemote jobWork at officeWorldwide- ...human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement... ...investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions Acts as...WebsiteFull timeWork experience placementWork at officeRemote workShift work
- ## Senior Clinical Research Associate - CNS/Rare Disease - Midwest - RemoteApplyremote type: Remotelocations: Research Triangle Park, North... ...submissions, TMF management, and in-house CRAs for projects with heavy site management needs.Through regular touchpoints and coaching...WebsiteRemote jobWork at officeWorldwide
$100 - $112 per hour
...with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote... ...will utilize your skills, knowledge, and clinical judgement to provide a high standard of... ...emergency situations based upon clinical research standards.Responsibilities :Responsible for...WebsiteWork at officeLocal areaRemote workNight shift- Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Remote, NC, United States Job ID: 25109784 Description... ...feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management...WebsiteInterim roleLocal areaImmediate startRemote work
$110k - $130k
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical... ...source data and study documentation. Support site activation and study conduct activities. Build strong...WebsiteLocal areaRemote workWorldwide- The Clinical Support Specialist provides critical operational and administrative... ..., Start-Up Managers, Clinical Research Associates (CRAs), and cross-... ...operating procedures (SOPs). Assist with study start-up activities... ...Start-Up Managers with site activation activities,...WebsiteContract workWork at office
$100k - $112k
...with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote... ...routine monitoring and close-out of clinical sites, maintenance of study files, conduct... ...management systems as assigned by management Assist with training of new employees, eg. co-...WebsiteWork at officeLocal areaRemote workNight shift- Clinical Research Associate II - Oncology (North Carolina/South Carolina) AbbVie’s mission is to... ...research, partner with investigators and site staff, and drive performance. Job... ...and recommends new investigators/sites, assisting placement of studies. Ensures quality data...WebsiteContract workTemporary workLocal area
$50k - $99k
...excellence. We are Worldwide Clinical Trials, and we are a global team... ...! What the In-House Clinical Research Associate II does at Worldwide... ...II (IHCRA) is responsible for site management tasks for studies in... ...oversight. What you will do Assist with feasibility questionnaires...WebsiteHourly payInterim roleWork at officeLocal areaRemote workWorldwide- Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge... ...intelligence and clinical research organization. We’re proud to... ...such as feasibility and site selection and reviews site usability... ...years ahead. Global Employee Assistance Programme, LifeWorks,...WebsiteWork experience placementWork at officeWork from homeFlexible hours
- ..., multimodal evidence that supports clinical, regulatory and strategic decision-making... ...Health is seeking a Senior Clinical Research Associate to conduct site management and data monitoring of... ...of all monitoring activities. Assist with site start-up activities, including...WebsiteWork at officeRemote work
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