Clinical Research Associate - Site Monitoring & Trials
$47.4k - $169.3kIQVIA
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 visits, managing site communication, and evaluating study practices. Ideal candidates should have a Bachelor's degree in a scientific field and possess strong communication and organizational skills. The role offers competitive compensation ranging from $47,400 to $169,300 annually, with additional benefits. #J-18808-Ljbffr
- ...A leading clinical research organization is seeking a Clinical Research Associate (CRA) to be part of their Durham... ...role requires conducting site visits, ensuring... ...and managing clinical trial execution. Candidates... ...have at least 1 year of monitoring experience and a background...Website
$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- ...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... ...activities associated with clinical trials to ensure timelines and metrics are met...WebsiteInterim role
$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 - $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...Website$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'...Website- ...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...WebsiteFull time
- ...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... ...You will work closely with investigative sites to ensure compliance and data integrity...Website
$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...Website$87.2k - $182k
...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...WebsiteWork at office- ...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...Website
$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...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’...Website
- ...CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1... ...Overview: We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key... ...the successful execution of clinical trials. In this position, you will be responsible...WebsiteImmediate start
$71.9k - $145.3k
...IQVIA is seeking Study Start‑Up Clinical Research Associates to join our Sponsor Dedicated teams... ...Start‑Up and at least 6 months of on‑site or in‑house monitoring experience. Candidates can be... ...of assigned sites for Phase I‑IV trials in the country in accordance with...WebsiteFull timePart timeLocal area$87.2k - $182k
...Job Overview Perform monitoring and site management work to ensure that sites... ...scope of work and Good Clinical Practice. Work with sites to... ...available for filing in the Trial Master File (TMF) and verify... ...applying, applicable clinical research regulatory requirements. Good...WebsiteFull timePart timeLocal area$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates... ...have 1-2 years of onsite monitoring experience with expertise... ...Overview Perform monitoring and site management work to ensure... ...for filing in the Trial Master File (TMF) verify that...WebsiteFull timePart timeLocal area$90k - $140k
...take healthcare and clinical research personally, with shared... ...a Clinical Research Associate II or Senior Clinical... ...Associate in experience in monitoring pain studies to join... ...monitoring and site management process in... ...documentation for clinical trials Provide mentoring,...WebsiteHourly payCurrently hiringLocal areaRemote work$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you'll play a crucial role... ...requirements. Essential Functions Site Monitoring: Conduct selection, initiation,... ...all site documents are filed in the Trial Master File (TMF) and Investigator's Site...WebsiteFull timePart timeLocal areaImmediate startWorldwide$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...WebsiteRemote workNight shift- ...Actalent is seeking a Lead Clinical Research Associate for a 12-month renewable contract in Durham, NC, available as a 10... ...contractor. In this role, you will oversee clinical monitoring and site management for multiple trials, ensuring compliance with regulatory standards....WebsiteContract workFor contractorsRemote work
$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking... ..., Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses... ...participants in clinical trials and respond to emergency situations... ...for all aspects of study site monitoring including routine...WebsiteWork at officeLocal areaNight shift$80k - $90k
...Fortrea's Monitoring Excellence Academy is hiring!! We are seeking... ..., Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses... ...participants in clinical trials and respond to emergency situations... ...for all aspects of study site monitoring including routine...WebsiteWork at officeLocal areaRemote workNight shift$101.6k - $169.3k
Job Overview Perform monitoring and site management work to ensure that sites... ...scope of work and Good Clinical Practice. Work with sites to... ...available for filing in the Trial Master File (TMF) and verify... ...applying, applicable clinical research regulatory requirements. Good...WebsiteLocal area$47.4k - $169.3k
Job Overview Perform monitoring and site management work to ensure that sites... ...requirements, i.e., Good Clinical Practice (GCP) and International... ...available for filing in the Trial Master File (TMF) verify... ...applying, applicable clinical research regulatory requirements (i.e...WebsiteFull timePart timeLocal area- ...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... ...in delivering high-quality clinical trials and improving healthcare. #J-18808-...Website
- ...Reporting to the Director, Clinical Quality Management, the Clinical Research Associate will collaborate... ...with investigative study sites to complete required site... ...-GCP, SOPs, Clinical Monitoring Plan (CMP), Protocol, Study... ...Phase II - IV clinical trials preferred Risk Based...WebsiteContract workLocal areaImmediate startRemote 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...Website- ...Experienced Clinical Research Associate - Full-Service- West Coast Updated: April 16, 2026... ...Research Associate responsible for site qualification, initiation, monitoring, management, and close-out... ...ISF) for accuracy; reconcile with Trial Master File (TMF); ensure archiving...WebsiteInterim roleLocal areaRemote work
$70.1k - $126.1k
...Description Experienced Clinical Research Associate - Sponsor Dedicated Syneos... ...Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities... ...contents of the ISF with the Trial Master File (TMF). Ensures the...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
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