Senior CRA I: Lead Site Monitoring & Compliance
IQVIA
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 years of monitoring experience. The CRA position offers opportunities for growth within a dynamic and collaborative environment, making a direct impact on patient outcomes. Join us in delivering high-quality clinical trials and improving healthcare. #J-18808-Ljbffr
- ...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...SeniorWebsite
- ...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 study progress...SeniorWebsite
$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 integrity checks, requiring 4+ years of clinical monitoring experience. The candidate must...SeniorWebsiteRemote workNight shift$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$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$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$87.2k - $169.3k
...A leading clinical research organization is seeking a Senior Clinical Research Associate (CRA) in Durham, North Carolina. Ideal candidates will... ...at least 1.5 years of on-site monitoring experience and a strong... ...strategies, and ensuring compliance with study protocols and...SeniorWebsite$101.6k - $169.3k
...The successful candidate will ensure high standards of study site practices, evaluate data integrity, and facilitate effective communication among stakeholders while driving project execution support. A competitive salary range of $101,600 to $169,300 is offered, along...SeniorWebsite$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 with study protocols, applicable regulations, and sponsor requirements. Candidates...SeniorWebsite- ...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 and data integrity while managing multiple site visits. This...SeniorWebsite
$64k - $189k
...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 is required, along with a nursing or relevant...Website- ...CRA 2/Senior CRA 1 Durham, United States of America | Full time... ...partner with investigative sites and cross-functional teams... ...executed with excellence, compliance, and patient focus. What you'll do: Lead and execute site monitoring visits (selection, initiation...SeniorWebsiteFull time
$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research Coordinators or Research... .... Responsibilities Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical...WebsiteWork at officeLocal areaNight shift$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research Coordinators or Research... .... Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical...WebsiteWork at officeLocal areaNight shift$90.2k - $175.1k
...Clinical Research Associate (CRA) to join our team and play a... ...partner with investigative sites and cross-functional teams to... ...executed with excellence, compliance, and patient focus. What You'll Do Lead and execute site monitoring visits (selection, initiation...SeniorWebsiteFull timePart timeImmediate startWorldwide$87.2k - $169.3k
...A leading clinical research organization in Durham, North Carolina, seeks a Senior Clinical Research Associate specialized in early clinical development. The candidate will monitor clinical sites to ensure compliance with protocols, manage subject recruitment strategies...SeniorWebsite$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- Scorpion Therapeutics is seeking a Senior Medical Director for Medical Monitoring to provide expertise and guidance in clinical development. The role involves... ...up-to-date knowledge of therapies and ensuring study compliance while working cross-functionally. Ideal candidates...SeniorWork at office
- ...Senior Medical Director - Medical Monitoring (UT Clinical & Medical Affairs) Responsibilities Provide medical expertise, advice, and guidance to clinical... ...medical inquiries from internal/external study teams and sites (including on‑call support) Conduct medical monitoring...SeniorWebsiteWork at office3 days per week
$147.6k - $196.8k
...experts - advance evidence and save lives by leading rigorous research and evaluation;... ...contribute to large‑scale implementation and monitoring initiatives for federal health agencies.... ...engagement strategies. Serve as a senior contributor to model testing, monitoring...Full timeWork experience placementH1bWork at officeRemote work- ...Senior Director - Operations - DRH Work Arrangement: On-Site Requisition Number: 269414 Regular or Temporary... ...Hospital. Through leading direct and indirect relationships... ..., performance and monitoring of operational and... ..., implementation and compliance with applicable DUHS...SeniorWebsiteTemporary workLocal area
- ...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
$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- Southern Company is seeking a Facilities Environmental Compliance Program Manager to lead the environmental compliance program across multiple manufacturing sites, including Durham. This role involves overseeing compliance efforts, managing a team, and interacting with...SeniorWebsiteLocal area
$87.2k - $169.3k
...Senior Clinical Research Associate (Sr. CRA 1) IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of two years of on-site monitoring experience in oncology. IQVIA Biotech is a full-service... ...company training. IQVIA is a leading global provider of clinical...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide$90k - $140k
...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... ...clinical monitoring and site management process in accordance... ...from the Clinical Team Lead role Provide feedback...SeniorWebsiteHourly payCurrently hiringLocal areaRemote work- ...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 compliance with protocols, and managing clinical... ...at least 1 year of monitoring experience and a...Website
- ...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’...SeniorWebsite
- ...Director (Must Have - Medical Monitoring - Oncology/Protocol Exp) Syneos Health is a leading fully-integrated life... ...members and clinical site staff; provides... ...Company is committed to compliance with the Americans with... ...studies. Interacts with senior management, customers,...WebsiteContract workWork at officeWorldwideFlexible hours
- ...Biotechnologies, we're leading the charge in... ...compliant manufacturing site, we thrive on collaboration... ...related to profit margin, monitoring and optimizing... ...required. Ensures compliance to all relevant internal... ...-functional teams and senior leadership to support...SeniorWebsiteContract work
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