Sponsor-Focused Clinical Research Associate - Monitoring
$87.2k - $182kIQVIA
IQVIA seeks an experienced Site Manager in North Carolina to perform monitoring and management tasks ensuring compliance with study protocols. You will lead monitoring visits, track regulatory submissions, and manage site documentation. Candidates must have a Bachelor's degree in a scientific discipline or healthcare and at least 1.5 years of on-site monitoring experience. Proficient use of Microsoft Office is essential. The role offers potential base pay ranging from $87,200 to $182,000 based on qualifications and experience. #J-18808-Ljbffr IQVIA
$71.9k - $189k
...Job Overview Perform monitoring and site management work to ensure... ...regulations and guidelines, and sponsor requirements. Essential... ...regulatory requirements, i.e., Good Clinical Practice (GCP) and... ...applying, applicable clinical research regulatory requirements (i.e....SuggestedFull timePart timeLocal areaImmediate startWorldwide$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring... ...and adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site Monitoring: Conduct selection, initiation, monitoring, and...SuggestedFull timePart timeLocal areaImmediate startWorldwide$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic... ...regulations and guidelines, and sponsor requirements. Essential Functions Perform...SuggestedFull timePart timeLocal area$71.9k - $145.3k
...IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house monitoring experience. Candidates can be located anywhere in the United...SuggestedFull timePart timeLocal areaImmediate startWorldwide$101.6k - $169.3k
A leading global provider of clinical research services is seeking a Senior Clinical Research Associate 1 to perform site monitoring and management. The role involves ensuring compliance... ...protocols, applicable regulations, and sponsor requirements. Candidates should have a...Suggested- IQVIA Argentina is seeking a Clinical Research Associate based in Durham, North Carolina, to perform monitoring and site management work. The role includes ensuring compliance with study protocols and regulatory requirements. Ideal candidates will hold a Bachelor's degree...Full time
$47.4k - $169.3k
A leading global provider of clinical research services is seeking a Clinical Research Associate in Durham, NC. This role involves monitoring clinical sites to ensure compliance with study protocols and regulatory requirements. The ideal candidate will have a bachelor'...- A biotechnology company is seeking a Clinical Research Associate in Durham, NC. The ideal candidate will have 4+ years of independent monitoring experience and a solid understanding of ICH and GCP guidelines. You will work closely with investigative sites to ensure compliance...
$47.4k - $169.3k
A global clinical research organization is seeking a Clinical Research Associate in Durham, NC. The position involves monitoring site activities to ensure compliance with study protocols and regulatory requirements. Key responsibilities include conducting site monitoring...- A leading clinical research organization is seeking a Clinical Research Associate (CRA) to be part of their Durham team. The role requires conducting site visits, ensuring... .... Candidates should have at least 1 year of monitoring experience and a background in life sciences....
- A leading clinical research organization in North Carolina is seeking a Clinical Research Associate (CRA 2) with at least 1 year of on-site monitoring experience, particularly in oncology. The role involves conducting site visits, ensuring compliance with study protocols...
$64k - $189k
IQVIA LLC is seeking an experienced Clinical Research Associate for their Durham, North Carolina location. This role involves significant travel (65-70%) to ensure compliance with study protocols across multiple sites. A minimum of 2.5 years of clinical research coordination...- ...with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we... ...Overview: We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key...Immediate start
- ...disease. Reporting to the Director, Clinical Quality Management, the Clinical Research Associate will collaborate closely with... ...with ICH-GCP, SOPs, Clinical Monitoring Plan (CMP), Protocol, Study... ...with experience at both CRO and Sponsor Rare disease or complex study...Contract workLocal areaImmediate startRemote work
$55k - $65k
...rewarding career. We are currently hiring an In-House Clinical Research Associate to join our team! As an In-House CRA here at Rho, you'll... ...CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents...Hourly payWork experience placementCurrently hiringLocal areaRemote work$70.1k - $126.1k
...Description Experienced Clinical Research Associate - Full-Service Syneos Health® is a leading... ...qualification, site initiation, interim monitoring, site management activities and close... ...attends Investigator Meetings and/or sponsor face to face meetings. Participates...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours- ...Description Experienced Clinical Research Associate - Full-Service- West Coast Syneos Health®... ...qualification, site initiation, interim monitoring, site management activities and close... ...attends Investigator Meetings and/or sponsor face to face meetings. Participates...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...market innovative medicines, solutions and services in more than 110 countries and regions. The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines,...Full timeInterim role
$85 - $90 per hour
12 month renewable contract 1099 ONLY High travel 7+ years of monitoring experience REQUIRED Job Title: Clinical Research Associate Responsibilities Participate in site selection and train site personnel regarding the trial. Perform routine site monitoring...Contract workTemporary workRemote work- ...disease. The Central Data Monitoring Specialist (CDMS) supports... ...oversight activities across clinical studies. This role partners... ...Clinical Operations, Clinical Research Associates, Data Management, and... ...centralized review activities and sponsor oversight. Good working...Remote work
- Experienced Clinical Research Associate - Full-Service- West Coast Updated: April 16, 2026 Location: Morrisville... ...for site qualification, initiation, monitoring, management, and close-out visits (on... ...in Investigator Meetings and sponsor meetings; attend clinical training...Interim roleLocal areaRemote work
$71.9k - $169.3k
IQVIA Argentina is seeking a Clinical Research Associate based in Durham, North Carolina, to perform site monitoring and management. The ideal candidate should have 1-2 years of monitoring experience, particularly in Cardiovascular, Oncology, or Neurology fields. Responsibilities...$70.1k - $126.1k
Syneos Health, Inc. is seeking a CRA II - Sponsor Dedicated for a home-based role in... ...responsibilities include site qualification, monitoring, and management activities, ensuring... ...communication skills, and have knowledge of Good Clinical Practice guidelines. The position offers...Remote jobWork from homeFlexible hours$71.9k - $169.3k
A leading clinical research organization is hiring a Clinical Research Associate (CRA) at the CRA 2 level. Candidates should have 1-2 years of onsite monitoring experience and be familiar with regulations in Cardiovascular, Oncology, or Neurology. This remote position...Remote work- ...biopharmaceutical company in Durham, NC seeks a Central Data Monitoring Specialist to ensure data quality oversight across clinical studies. Ideal candidates will have a Bachelor'... ...in the biopharmaceutical industry. The role focuses on identifying data issues and ensuring the...
$73.7k - $117.92k
...organizations as part of the Financial Monitoring & Analysis (“FMA”) team within our Diversified... ...in North Carolina and beyond, focused on improving healthcare outcomes, affordability... ..., Financial Statement Modeling, Market Research, Market Research Analysis, Mergers and...Work at officeLocal areaRemote workFlexible hoursShift work2 days per week$22.61 - $34.27 per hour
...more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,... ...analyze food intake, which is essential for monitoring and improving human health. We are... ...conducting detail‑oriented experiments with a focus on precision and efficiency. We seek...Work experience placement- ...,600 faculty physicians and researchers, nearly 2,000 students, and... ...Biomedical Engineering and is focused on the development and... ...colony Weaning, breeding, and monitoring mice Collection and preparation... ...department. #J-18808-Ljbffr Duke Clinical Research InstituteCurrently hiring
- ...University Hospital, Epilepsy Monitoring Unit Job Summary... ...in patient care, research, and teaching, and... ...Provide and coordinate clinical care for service-specific... ...conditions, and associated procedures or interventions... ...Able to remain focused and organized Able...Monday to FridayFlexible hoursWeekend workWeekday work
- ...duties including animal health monitoring, animal husbandry, and... ...maintain quality and health of research animals to include daily feed... ...as required. • Maintains focus on animal welfare reporting all... ...completing all documentation associated with the task. • Cleans assigned...Weekend work
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