CRA II: Site Management & Monitoring Expert
Syneos Health Inc
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 performing site qualifications, managing data integrity, and collaborating with study sites. The role requires up to 75% travel and entails working in a fast-paced environment to drive successful clinical trials. #J-18808-Ljbffr
$87.2k - $145.3k
...Associate in Durham, North Carolina. This role involves performing site monitoring visits, ensuring compliance with regulatory guidelines, and managing study progress. Candidates should have 1.5 to 2 years of CRA experience and a Bachelor’s Degree in a scientific discipline...Website$125k - $140k
...FTINC Fortrea Inc. is looking for an Oncology Senior CRA 2 to oversee site monitoring and coordinate clinical projects. The role requires 5+ years... ...and have a strong understanding of data integrity management. The position offers a competitive salary between $125,0...WebsiteRemote workNight shift- ...IQVIA LLC is seeking a Clinical Research Associate (CRA) to advance clinical research and patient outcomes. This role involves leading site monitoring visits, ensuring compliance, and managing study progress. You will collaborate with cross-functional teams and build...Website
- ...IQVIA is seeking a Clinical Research Associate (CRA) to advance clinical research. In this role, you will lead site monitoring visits and ensure study execution compliance and data integrity. Ideal candidates have a Bachelor's degree in life sciences and at least 1.5...Website
- ...The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP... ...and/or co-monitors as required with CRO and CRA staff to insure study integrity and compliance. Reviews...WebsiteInterim role
- ...Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate (CRA) to manage research activities across diverse therapeutic areas. The role requires excellent communication skills, a strong organizational ability, and a proficiency in Microsoft Office...WebsiteWork at officeWorldwide
- ...Research Organization is seeking an experienced Senior Clinical Research Associate (CRA) for an opportunity in North Carolina. The role involves conducting site visits and monitoring activities across various studies. The ideal candidate will have 3-5 years of on-site...WebsiteRemote 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
- 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
$71.9k - $119.9k
...A leading biotech company in North Carolina is hiring a Clinical Research Associate I (CRA I) to support clinical research studies. The role involves on-site monitoring, ensuring compliance with protocols and regulations, and maintaining strong communication with investigative...Website$90k - $140k
...hiring a Clinical Research Associate II or Senior Clinical Research Associate in experience in monitoring pain studies to join our team! As our next CRA II or Senior CRA, you will play an... ...of the clinical monitoring and site management process in accordance with ICH Good...WebsiteHourly payCurrently hiringLocal areaRemote work- ...is seeking a Clinical Research Associate (CRA) to advance clinical research and improve patient... .... In this role, you’ll be responsible for site monitoring visits, ensuring compliance with GCP/ICH guidelines, and actively managing study progress. The ideal candidate will...Website
$125k - $132k
...Fortrea is seeking an Unblinded Sr. CRA 1 to ensure high standards of care during clinical... ...trials. The role involves comprehensive site monitoring, regulatory compliance, and data... ...fast-paced, technology-oriented teams and manage 50-60% overnight travel. This remote position...WebsiteRemote workNight shift$125k - $132k
...FTINC Fortrea Inc. is seeking an Unblinded Sr. CRA 1 to join their FSP team in the United States. The ideal candidate will monitor clinical sites, ensuring that regulations are followed and data integrity is maintained. Responsibilities include training staff and coordinating...WebsiteLocal areaRemote workNight shift$71.9k - $169.3k
...IQVIA LLC is seeking a Clinical Research Associate (CRA) in Durham, NC, to manage clinical trial sites and ensure compliance with study protocols. You will conduct monitoring visits, collaborate with site staff, and ensure the integrity of clinical research data. Candidates...Website$71.9k - $169.3k
...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... ...and organizational skills, and the ability to manage study progress. The potential base pay ranges...Remote work$105.5k - $140k
...option. Who You Are The Monitoring Team Lead/Senior Monitoring... ...activities, and support of study sites to ensure compliance with... ...analytics reviews, and site management tasks to support monitoring efforts... ...Provide feedback on CRA performance to Clinical Monitoring...WebsitePermanent employmentContract workWork at officeRemote work- ...intended to become a Retail Personal Banker II after completing a 4-8 week on-boarding... ...by consistently identifying, assessing, managing, monitoring, and reporting risks of all types.... ...Mortgage Licensing System (NMLS). The NMLS web site (mortgage.nationwidelicensingsystem.org)...WebsiteWork experience placementWork at office
- ...Associate in Raleigh, NC. The role involves overseeing and managing clinical trial activities to ensure compliance with... ...a Bachelor's degree and extensive experience as a CRA, alongside strong skills in monitoring, problem-solving, and stakeholder management. ICON offers...
$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...WebsiteWorldwide$70.1k - $126.1k
...CRA II - Sponsor Dedicated (Home-Based - FL / GA) Updated: May 4, 2026 Location: Morrisville, NC, United... ...Job ID: 25108402 Job Responsibilities Perform site qualification, site initiation, interim monitoring, site management activities and close‑out visits (on‑site or...WebsiteInterim roleLocal areaRemote workWork from homeFlexible hours$64k - $189k
..., 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 is required, along with a nursing or relevant university degree. The position...Website- ...Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site interactions and ensure safety and compliance within clinical trials. Responsibilities include managing project timelines, supporting team training, and maintaining...Website
$80k - $90k
...Position Overview Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Coordinators... .... Responsibilities All aspects of study site monitoring, including routine monitoring... ...data for missing or implausible entries. Manage registry activities as outlined in...WebsiteLocal areaRemote workNight shift$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology... ...Responsible for all aspects of study site monitoring including routine monitoring... .... Responsible for all aspects of site management as prescribed in the project plans....WebsiteWork at officeLocal areaNight shift$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology... ...:Responsible for all aspects of study site monitoring including routine monitoring... ...-Responsible for all aspects of site management as prescribed in the project...WebsiteWork at officeLocal areaNight shift- ...progression; supportive and engaged line management; technical and therapeutic area... .... Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and... ...For Real World Late Phase, the CRA II will use the business card title...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Country Lead Monitor ICON plc is a world-leading healthcare intelligence and clinical... ...clinical development As a Clinical Trial Manager at ICON, you will manage clinical trial... ..., among others. Visit our careers site to read more about the benefits ICON offers...WebsiteLocal areaFlexible hours
- ...Country Lead Monitor ICON plc is a world-leading healthcare intelligence and clinical... ...clinical development. As a Clinical Trial Manager at ICON, you will manage clinical trial... ...assessments, among others. Visit our careers site to read more about the benefits ICON...WebsiteLocal areaFlexible hours
- ...conducting environmental and clean utility monitoring and standard microbiological assays. The... ...are promptly escalated to laboratory management. Tasks will be assigned to off‑shift personnel... ...to our cGMP‑compliant manufacturing site, we thrive on collaboration, creativity,...WebsiteTemporary workFlexible hoursShift work
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