Clinical Research Associate II: Site Monitoring
Allen Spolden
A leading clinical research company in North Carolina is seeking a Clinical Research Associate to provide support for all clinical trials. The role involves preparing protocols, monitoring studies, and ensuring compliance with guidelines. Ideal candidates should have a bachelor's degree and 1-2 years of clinical research experience. Strong attention to detail, integrity, and excellent communication skills are essential. This position offers an opportunity to contribute to impactful clinical research projects. #J-18808-Ljbffr Allen Spolden
- Grifols, S.A is seeking a Clinical Research Associate in North Carolina to ensure site adherence to regulatory requirements and GCP Guidelines. You will manage site start-up and monitor clinical trials while maintaining project timelines and compliance. The ideal candidate...Website
- Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate...Website
- Syneos Health/ inVentiv Health Commercial LLC is hiring an Experienced Clinical Research Associate in North Carolina. This role involves site management, regulatory compliance, and ensuring that clinical trials operate smoothly. Candidates should have a Bachelor's degree...WebsiteRemote jobFlexible hours
$70.1k - $126.1k
Syneos Health, Inc. is seeking a CRA II - Sponsor Dedicated for a home-based... ...Morrisville, NC. The responsibilities include site qualification, monitoring, and management activities, ensuring... ...skills, and have knowledge of Good Clinical Practice guidelines. The position...WebsiteRemote jobWork from homeFlexible hours- ...on 07/16/2025 Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City Columbus... ...in the evaluation of potential clinical sites according to established criteria of acceptability... ...materials. Conduct ongoing study monitoring, including frequent periodic site...WebsiteWork experience placement
- ABOUT THE JOB The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials... ..., interim, and close‑out site visits. Manage and train site... ...supporting CRA I and CRA II staff by providing solutions...WebsiteInterim roleWork at office
- Clinical Research Associate II - Oncology (North Carolina/South Carolina) AbbVie’s mission is to discover... ...research, partner with investigators and site staff, and drive performance. Job... ...Conduct site evaluation, training, routine monitoring, and closure activities in compliance...WebsiteContract workTemporary workLocal area
- Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a leading... .... Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and... ...World Late Phase, the CRA II will use the business card title...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- A leading life sciences organization is looking for a Clinical Research Associate to oversee site management and ensure compliance with regulatory guidelines. The ideal candidate will have a Bachelor's degree and strong communication skills, with responsibilities including...Website
$120k - $140k
...the time! Develops strong investigative site relationships and ensures continuity of... ...study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance... ...to upper management Work with in-house Clinical Trial Assistant to collect, review, and...WebsiteInterim roleLocal areaRemote workFlexible hours- ...The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical...WebsiteLocal areaRemote work
- ...strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for... ...delivery of the studies at allocated sites and is an active participant in the... ...site and has the responsibility for monitoring the study conduct to ensure proper delivery...WebsiteLocal areaRemote workFlexible hoursShift work
- ...Description Experienced Clinical Research Associate - Full-Service- West Coast... ...Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and... ...Real World Late Phase, the CRA II will use the business card title...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Position: Senior Clinical Research Associate (level dependent on experience) Location: Raleigh, NC Job... ...You’ll Do Manages investigative site activity for multiple protocols/indications... ...site visits (pre‑study, initiation, monitoring, and close‑out) and completes site...WebsiteLocal areaRemote workWork from homeHome office
- 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...WebsiteInterim role
- Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research... ...You will lead on clinical trial monitoring tasks requiring technical depth, with... ...improvement. Monitoring clinical trial sites to ensure adherence to study...WebsiteFlexible hours
$55k - $65k
...We are currently hiring an In‑House Clinical Research Associate to join our team! As an In‑House CRA... ...CRA on a clinical trial to ensure that monitoring activities are properly supported and... ...Collect, track and review investigational site records relating to subject screening...WebsiteHourly payWork experience placementCurrently hiringLocal areaRemote work- Parexel is seeking a Clinical Research Associate (CRA) in Raleigh, North Carolina. The CRA will manage site monitoring and close-out of assigned clinical trial investigator sites to ensure patient safety and compliance with good clinical practices (GCP). Responsibilities...Website
- ...airport. Job Purpose: The Site and Monitoring Health Lead (SMH Lead) will... ...safeguard the quality of clinical trial execution at... ...work directed by the client Associate Director (or above), Site and... ...Study Management/Clinical Research Organization (CRO) to mitigate...WebsiteLocal areaRemote work
- ...Country Lead Monitor ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation... ..., among others. Visit our careers site to read more about the benefits ICON offers....WebsiteLocal areaFlexible hours
$63.93k - $99.49k
...and the Exceptional Children (EC) Division, particularly during monitoring and improvement processes. Job Responsibilities:... ...training, staff development, and technical assistance through on-site visits, conferences, and virtual methods. Monitor compliance...WebsiteWork at officeLocal area- ...become a Retail Personal Banker II after completing a 4-8 week on... ..., assessing, managing, monitoring, and reporting risks of all types... ...Licensing System (NMLS). The NMLS web site (mortgage.... ...-DH2 Retail Personal Banker Associate II At Fifth Third, we understand...WebsiteWork experience placementWork at office
- UtilityInnovation Group (UIG) is hiring a Grid Monitoring Specialist to support our GridSure Command Center. The GridSure Command Center... ...disaster response events impacting energy assets Support Factory and Site Acceptance Testing (FAT/SAT) and verify system integrity Assist...WebsiteWork at officeRemote workWorldwide
- .Digital R&D Engineer - Monitoring & Communications page is loaded## Digital R&D Engineer - Monitoring & Communicationslocations: Raleigh... ...limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable...WebsiteFull timeRemote workWorldwideFlexible hours
- A healthcare organization in North Carolina seeks a Clinical Nurse IV to provide expert nursing care in the Progressive Care Unit. This role... ...a tertiary care setting. The position offers full-time hours on-site with a competitive salary range, promoting a diverse and...WebsiteFull time
- A leading clinical research organization is seeking an experienced Clinical Research Associate in Morrisville, NC. The role involves site qualification, monitoring, and ensuring compliance with regulatory guidelines. The ideal candidate holds a Bachelor's degree or RN and...WebsiteRemote job
- A leading biopharmaceutical solutions organization is seeking an Experienced Clinical Research Associate to oversee site monitoring, ensuring compliance with regulatory requirements and clinical protocols. Responsibilities include conducting site visits, managing site...WebsiteRemote jobWorldwide
$115k - $125k
Senior Clinical Research Associate Piper Companies is currently seeking aSenior Clinical Research Associate (CRA) for an opportunity... ...Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple study Responsible...WebsiteRemote work- Experienced Clinical Research Associate - Full-Service- West Coast Updated: April 16, 2026 Location: Morrisville, NC, United States... ...Clinical Research Associate responsible for site qualification, initiation, monitoring, management, and close-out visits (on-site or remote...WebsiteInterim roleLocal areaRemote work
- ICON Clinical Research is looking for a Senior Clinical Research Associate in Raleigh, North Carolina. You will oversee clinical trial activities to ensure they... ...standards. Responsibilities include monitoring trial sites, conducting site visits, and providing training...Website
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