Sponsor-Dedicated CRA: Travel-Heavy Monitoring
$64k - $189kIQVIA LLC
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 is required, along with a nursing or relevant university degree. The position offers competitive compensation ranging from $64,000 to $189,000 based on experience and qualifications, along with various benefits. #J-18808-Ljbffr IQVIA LLC
- Fortrea is looking for an Unblinded CRA to join their FSP team in Durham, NC. The successful candidate will monitor clinical trial sites, ensuring adherence to protocols and standards. Responsibilities include site management, training new staff, and reporting adverse events...TravelRemote work
- ...Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location:... ...qualification, initiation, monitoring, management, and close‑out... ...Ability to manage required travel of up to 75% on a regular basis... ...within Clinical Monitoring/CRA oversee and ensure the integrity...TravelInterim roleRemote workFlexible hours
- ...in the United States is seeking Unblinded CRAs with 1-3 years of monitoring experience who reside in the U.S. The role involves 8-10 days on site per month with a mix of onsite and remote work, and travel expected in the range of 50-60% overnight. Open to West Coast, Central...TravelRemote jobNight shift
$50.02 - $62.53 per hour
Mission+ in Durham, NC is looking for a Clinical Research Associate 3 to oversee Phase 1 oncology studies. The role involves monitoring site performance, ensuring compliance with protocols, and conducting both onsite and remote assessments. Ideal candidates will have at...SuggestedContract workRemote work$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- Belcan is seeking a Clinical Research Associate in Durham, North Carolina, for a 12-month assignment. Responsibilities include monitoring Phase 1 oncology studies, providing oversight of site performance, and ensuring compliance with protocols. Candidates should have strong...
$105k - $117k
Fortrea is seeking Experienced Device CRA 2s to lead and support their Medical Device... ...Durham, North Carolina. The role involves monitoring clinical study sites, ensuring protocols... ...experience. The position involves 60-70% travel and offers comprehensive benefits, including...TravelRemote job- ...Title : Clinical Research Associate/Clinical Monitor Duration : 12+ Months Primary Responsibilities Serve as the sponsor-side point of contact for assigned sites, providing... ...experience in a sponsor-side or sponsor-dedicated CRA role is preferred; candidates should...Local areaRemote work
$64k - $189k
...Clinical Research Associate, Sponsor Dedicated page is loaded## Clinical Research Associate, Sponsor... ...regions.****Job Overview** Perform monitoring and site management work to ensure that... ...**Position requires 65-70% nationwide travel.****Essential Functions** • Perform site...TravelFull timePart timeLocal areaImmediate startWorldwide$95k - $175.7k
...Project Manager II - Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA... ...project management team members and clinical monitoring staff. Qualifications Bachelor’s... ..., both written and spoken. Ability to travel as necessary (approximately 25%). Benefits...TravelRemote jobContract workFlexible hours- ...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...
$71.9k - $182k
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level in Durham, North Carolina. Candidates will perform monitoring and site management work to ensure compliance with study protocols, focusing on areas like Cardiovascular, Oncology, and Neurology. Ideal...$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...- Duke University Hospital in Durham, NC, is seeking a dedicated Intraoperative Neuromonitoring professional to perform specialized procedures... ...from preoperative to postoperative care, with possible travel among Duke Health hospitals as needed. #J-18808-Ljbffr Duke Clinical...Travel
- ...oncology trials. The ideal candidate will possess strong oncology monitoring experience and the ability to apply clinical judgment while... ...collaborative oversight of study processes, and the opportunity to travel to investigative sites as required. A minimum of 5 years of...TravelRemote work
- 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...
$90.2k - $175.1k
IQVIA in Durham, NC is seeking a Clinical Research Associate (CRA) with onsite monitoring experience in oncology to join their team. The successful candidate will play a key role in delivering high-quality clinical trials by leading site visits and ensuring compliance with...- ...Clinical Research Associate - Sponsor Dedicated Syneos Health® is a... ...qualification, site initiation, interim monitoring, site management activities... ...Real World Late Phase, the CRA II will use the business... ...Ability to manage required travel of up to 75% on a regular...TravelContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...assists in the management of the clinical monitoring process to ensure site adherence to... .../or co-monitors as required with CRO and CRA staff to insure study integrity and compliance... ...assigned project. Ability and willingness to travel. Requirements: Associate’s degree in a...TravelInterim role
$69.8k - $226.8k
...seamlessly and adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site Monitoring: Conduct selection, initiation, monitoring, and... ...team members to support project execution. Travel : 6-10 DoS per month typical expectation, can be...TravelFull timePart timeLocal areaImmediate startWorldwide- Fortrea's Monitoring Excellence Academy is hiring Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years... ...and French-speaking candidates in Montreal, Canada. Willing to travel 65-70%. You will monitor clinical sites, ensure protocol...Travel
- PowerSecure, Inc. is seeking a diligent 24/7 Monitoring Operator to support its PowerControl Platform in a hybrid role. You will monitor... ...pressure environment. Remote work-from-home shifts are possible with travel to Durham when required. #J-18808-Ljbffr PowerSecure, Inc.TravelRemote jobWork from homeShift workRotating shift
- ...potential based on performance and budget. Responsibilities include sponsor-side oversight of site performance, protocol execution, and... ...conduct across the trial lifecycle, with on-site and remote monitoring in Phase 1 oncology studies and collaboration with CROs and...Remote work
- ...seeking a Clinical Research Associate (CRA) to serve as sponsor-side clinical operations representative for Phase 1 oncology trials, with monitoring oversight across sites and... ...with CRO partners and vendors. Regular travel to investigative sites is required. The...Travel
- ...Clinical Research Associate (CRA) serves as a sponsor-side clinical operations... ...other therapeutic areas monitoring oversight a plus. This role... ...preferred. This is a contract traveling CRA position, as needed.... ...a sponsor‑side or sponsor‑dedicated CRA role is preferred;...TravelContract workRemote work
$95k - $175.7k
...Project Manager II – Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA... ...project management team members and clinical monitoring staff. Qualifications:... ...both written and spoken. Ability to travel as necessary (approximately 25%)....TravelContract workImmediate startRemote workFlexible hours- ...oversee site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance... ...site training and audit readiness. Travel up to 75% is required; strong... ...for coordinating with investigators and sponsor teams. #J-18808-Ljbffr Syneos Health/ inVentiv...Travel
$71.9k - $145.3k
...IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring... ...CRO purpose-built to serve biotech sponsors. With over 25 years of experience... ...regulations (GCP/ICH). ~ Ability to travel as required by the project....TravelFull timePart timeImmediate startWorldwide$105k - $125k
...hub locations on the West Coast. 60-70% travel, 8-10 DOS per month. WHAT YOU WILL DO... ...Responsible for all aspects of study site monitoring including routine monitoring and close-... ...experience ~ Ophthalmology experience as a CRA ~ Open to various hub locations...TravelFull timePart timeWork at officeLocal areaRemote workFlexible hours- ...Associate III to oversee Phase 1 oncology trials and sponsor oversight, including site monitoring, risk identification, and CRO/vendor collaboration. The... ...manage complex protocols, timelines, and data integrity. Travel to investigative sites is required as needed. #J-1880...Travel
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