Clinical Lab Technician - Specimen Processing & Phlebotomy
Duke University
Duke University Health System's Clinical Laboratories seeks a Clinical Laboratory Technician to ensure proper collection of blood specimens and assist in delivering them to the appropriate laboratory. Location: Duke University Hospital; Schedule: Mon-Fri 7pm-1:30am.
Eligible for relocation and commitment bonuses as noted. The role requires basic phlebotomy skills, specimen processing, and strong communication with patients and staff.
#J-18808-Ljbffr$71.9k - $189k
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...SuggestedFull timePart timeLocal areaImmediate startWorldwide$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety of therapeutics... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...SuggestedFull timePart timeImmediate startWorldwide$90.2k - $175.1k
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...SuggestedFull timePart timeImmediate startWorldwide$74.5k - $197.5k
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals... ...relationships with investigative sites and provide protocol, process, and study-specific training.Monitor study progress, including...SuggestedFull timePart timeWork at officeImmediate startWorldwide$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...SuggestedFull timePart timeWork at officeLocal areaImmediate startWorldwide$90.2k - $175.1k
IQVIA is now hiring for Clinical Research Associates located on the West Coast and East Coast, US to join our growing Early Clinical Development... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...Full timePart timeImmediate startWorldwide$79.5k - $158.5k
...Clinical Research Associate IIWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for... ...laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any...Work at officeRemote workWorldwide$100k - $112k
...WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in... ...when requested Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs Independently...Work at officeLocal areaRemote workNight shift- ...re improving health and improving lives. Labcorp is seeking a Specimen Processor to join our team in RTP, NC . Work Schedule: Tuesday... ...or GED Preferred Qualifications 3 months or more of specimen processing experience 3 months or more of medical or laboratory experience...Temporary workCasual workInternshipFlexible hoursShift work
- ...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright... ...of regulatory documentation and support of contract and budget processes.Conduct all types of monitoring visits: Pre-Site Selection...Hourly payContract workInterim roleWork from homeWorldwide
- ...Clinical Research Associate (CRA) – 1099 Independent Contractor Department: Clinical Operations Contract Type: 1099 Independent... ...Facilitate site activation, contract execution, and budget processes. Support investigator site payment tracking and follow-up....Contract workFor contractorsWork at office
$64k - $189k
...Clinical Research Associate, Sponsor Dedicated Perform monitoring and site management work to ensure that sites are conducting the... ...health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...Full timePart timeImmediate startWorldwide$79.5k - $158.5k
...Make an Impact as a Clinical Research Associate II at Worldwide As a Clinical Research Associate II, you'll play a critical role in... ...laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any...Hourly payWork at officeLocal areaWork from homeWorldwide$35.8k - $123k
Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining... ...applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All...Full timePart timeImmediate startWorldwide$40.87k - $52k
Clinical Research Assistant Position Number: 00059787 | Location: Chapel... ...vendors, sample acquisition, processing and shipping, and maintaining... ...live tissue acquisition and specimen distributions. These... ...Requirements Carcinogen handlers (Lab workers) Evening work...Permanent employmentFull timeMonday to FridayNight shiftRotating shiftWeekend workAfternoon shift- ...Lab AssistantLabcorp is a global leader in laboratory services, providing... ...PMJob ResponsibilitiesReceive and sort clinical lab specimensPrepare specimens for testing and analysisScan and/or... ...3 months or more of specimen processing experience3 months or more of medical...Temporary workCasual workInternshipFlexible hoursShift work
- ...improving lives. Labcorp is seeking a Lab Assistant to join our team in RTP,... ...~ Receive and sort clinical lab specimens ~ Prepare specimens for testing... ...~3 months or more of specimen processing experience ~3 months or more of...Temporary workCasual workInternshipFlexible hoursShift work
$20.75 - $24 per hour
...Job Title: Research Technician Job Description The Research... ...and biospecimen processing core facility that underpins... ...active basic, translational, and clinical research studies. In this role... ...sensitive requests to obtain specimens from clinical areas or incoming...Permanent employmentContract workTemporary workMonday to FridayNight shiftWeekend workAfternoon shiftEarly shift- ...documentation for a range of dosage form batches and finished clinical trial packs of Investigational Medicinal Products in accordance... ...support to business partner areas relating to quality matters and process improvement. • Develop and incorporate effective processes and...Work experience placementWorldwideShift workDay shift
- ...non-technical procedures required to process and submit specimens Assigns specific computer generated identification... ...Learn and keep familiar with lab procedures and location of stored... ...Qualifications 1 to 3 yrs Experience in a Clinical Lab High School Diploma or equivalent...Contract workShift work
- ...Clinical Research AssistantEssential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance...
$71.32 - $76.32 per hour
...initiation, monitoring, and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive, and track subject...Temporary workLocal area- ...IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team in the United States. You will conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory...
$90.2k - $175.1k
...Clinical Research Associate position supporting Phase I early clinical development trials across multiple US locations. The role involves conducting site visits, monitoring protocol compliance, managing enrollment, and ensuring data integrity while working with cross-...$74.5k - $197.5k
...IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials in therapeutic areas including CNS, cardiovascular, obesity, and NASH/MASH. The role involves site management, regulatory compliance, protocol training, and cross-functional...Work at office$90.2k - $175.1k
...IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing...$79.5k - $158.5k
...Clinical Research Associate II position supporting psychiatry trials at a global CRO. The role involves on-site and remote monitoring activities, site relationship management, and data verification for clinical trials. Remote-eligible position based in Durham, North Carolina...Work at officeRemote work$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology monitoring experience for field-based work on the West Coast. The role involves managing clinical trial sites, monitoring protocol adherence, and ensuring data integrity while working 8-10 days on-site monthly...Local areaNight shift- ...Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience...Contract workWork at office
$125k - $140k
...Fortrea seeks a senior clinical research associate with 5+ years of monitoring experience for ophthalmology and oncology trials in the Midwest. This role involves comprehensive site monitoring, protocol compliance verification, data integrity oversight, and serious adverse...Night shift
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