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
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated job at Lensa. Durham, NC. Lensa is the leading career site for job seekers at every stage of their... ...hub. Oncology experience preferred. Job Overview Perform monitoring and site management work to ensure that sites are conducting...SuggestedFull timePart timeLocal areaWorldwide$71.9k - $189k
...IQVIA Argentina is seeking a dedicated Clinical Research Associate to perform site monitoring in Durham, NC. This role involves collaborating with study teams, ensuring compliance with Good Clinical Practice, and managing ongoing projects. Ideal candidates should have...Suggested$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$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 area$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...Full timePart timeLocal area- ...The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of an accelerated study start-up including...Interim role
- ...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...
- ...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,... ...execution. Candidates should have at least 1 year of monitoring experience and a background in life sciences....
$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...$71.9k - $189k
...IQVIA LLC is hiring a Clinical Research Associate 2 to ensure compliance and manage site monitoring in various clinical trials. The ideal candidate will have at least one year of on-site monitoring experience and a Bachelor's degree in a relevant field. This role offers...Worldwide- ...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 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...$70.1k - $126.1k
...Description Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is a leading fully-integrated life sciences services... ...Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours$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...- ...IQVIA is seeking a Clinical Research Associate (CRA) in Durham, North Carolina, to lead and execute clinical trial monitoring visits. In this role, you will ensure studies are executed with compliance and a patient-focused approach. The ideal candidate has a Bachelor’s...
$87.2k - $169.3k
...Senior Clinical Research Associate, Early Clinical Development page is loaded## Senior Clinical Research... ..., you will be responsible for monitoring and managing clinical sites to ensure... ...protocols, regulatory requirements, and sponsor expectations. Your work will directly...Full timePart timeImmediate startWorldwide$90k - $140k
...team who take healthcare and clinical research personally, with shared... ...hiring a Clinical Research Associate II or Senior Clinical Research... ...Associate in experience in monitoring pain studies to join our... ...pass an audit by Rho, the Sponsor, or a regulatory agency....Hourly payCurrently hiringLocal areaRemote work- ...divh2Clinical Research Associate 2, IQVIA/h2pDurham, United States of America |... ...| R1538099/ppIQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH,... ...regulations and guidelines, and sponsor requirements./ppEssential Functions...Full timeLocal area
- ...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 experience...Contract workLocal areaImmediate startRemote work
$116k - $155k
...Quality Management Data Monitor As a Principal Risk... ...role in shaping how clinical trial data is monitored... ...phases of clinical research. You'll collaborate closely... ...processes (CDPs) and associated study risks Support... ..., and stay laser focused on patient safety and...Temporary work- ...world's health. From clinical trials to regulatory,... ...and inspection ready. Monitor and maintain compliance... ...SOPs, other Parexel / Sponsor training requirements... ...presentation skills. Client focused approach to work.... ...experience in clinical research, with understanding of...Local areaImmediate startRemote workFlexible hours
$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 workWork from homeFlexible hours$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$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...- ...Experienced Clinical Research Associate - Full-Service- West Coast Updated: April 16, 2026 Location:... ...for site qualification, initiation, monitoring, management, and close-out visits (on... ...participate in Investigator Meetings and sponsor meetings; attend clinical training...Interim roleLocal areaRemote work
- ...Actalent is seeking a Lead Clinical Research Associate for a 12-month renewable contract in Durham, NC, available as a 1099 contractor. In this role, you will oversee clinical monitoring and site management for multiple trials, ensuring compliance with regulatory standards...Contract workFor contractorsRemote work
$19 per hour
...Weekly or Daily Pay options! Free state security training, sponsored by Allied! Career advancement opportunities! Excellent benefits... ..., disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic...Hourly payWeekly payDaily paidFull timePart timeWork at officeLocal area- ...IQVIA LLC in Durham, North Carolina, is seeking a Clinical Research Associate (CRA) to advance clinical research and improve patient outcomes. In this role, you’ll be responsible for site monitoring visits, ensuring compliance with GCP/ICH guidelines, and actively managing...
- ...drugged driving at no charge, serving 1 person every 8 minutes through local MADD victim advocates at 1-877-MADD-HELP. The Court Monitor Program works towards the elimination of drunk driving by observing court and collecting information on drunk driving cases. As one...Local area
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