FSP Clinical Research Associate 2 - Salt Lake City, Utah - Oncology
$100k - $112kFortrea
Fortrea seeks a Clinical Research Associate 2 with 2+ years of monitoring experience for an oncology position based in Salt Lake City, Utah. The role involves site monitoring, data integrity oversight, and regulatory compliance across clinical trials, with 8-10 days monthly on-site work.
Responsibilities
- Conduct routine and close-out monitoring of clinical sites and maintain study documentation
- Verify informed consent procedures and protocol adherence for patient protection
- Review Case Report Forms and generate data queries to ensure accuracy and completeness
- Manage Serious Adverse Event reporting and follow-up documentation
- Support site initiation, staff training, and local project coordination as needed
Requirements
- 2 years of clinical monitoring experience
- University degree or certification in allied health profession
- 60% overnight travel capability
- Proficiency with electronic data collection systems
- Strong organizational and communication skills
Compensation: $100,000-$112,000
$100k - $112k
...Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site... ...Denver, Colorado area with Oncology. WHAT YOU WILL DO You... ...your skills, knowledge, and clinical judgement to provide a... ...situations based upon clinical research standards....SuggestedWork at officeLocal areaRemote workNight shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology monitoring experience for field-based work on the West Coast. The role involves managing clinical trial sites, monitoring protocol adherence, and ensuring data integrity while working 8-10 days on-site monthly...SuggestedLocal areaNight shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with 2 years of monitoring experience for oncology clinical trials in the Denver area. The role involves site monitoring, data integrity verification, and regulatory compliance across mixed onsite and remote work, with approximately...SuggestedLocal areaRemote workNight shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology experience to monitor clinical trial sites in the Las Vegas area. The role involves 8-10 days monthly on-site work, combining monitoring activities, data integrity checks, and site management across multiple study...SuggestedNight shift$71.9k - $182k
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Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your... ...Experience: Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.Knowledge: Strong understanding of GCP...Full timePart timeWork at officeLocal areaImmediate startWorldwide$125k - $140k
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- ...excellence. We are Worldwide Clinical Trials, and we are a global team... ...data that advances clinical research.In this role, you'll serve as... ...home-based Clinical Research Associate role supporting sites across... ...experience monitoring Oncology clinical trials.Requires travel...Hourly payContract workInterim roleWork from homeWorldwide
$74.5k - $197.5k
...IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials in therapeutic areas including CNS, cardiovascular, obesity, and NASH/MASH. The role involves site management, regulatory compliance, protocol training, and cross-functional...Work at office- ...Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience...Contract workWork at office
$79.5k - $158.5k
...Make an Impact as a Clinical Research Associate II at Worldwide As a Clinical Research Associate II, you'll play a critical role in ensuring clinical studies are conducted to the highest standards of quality, compliance, and patient safety. Your work will directly support...Hourly payWork at officeLocal areaWork from homeWorldwide$79.5k - $158.5k
...Worldwide Clinical Trials seeks a Clinical Research Associate II with 2–3 years of monitoring experience to support oncology trial execution. The role involves conducting site monitoring visits, ensuring protocol compliance and data integrity, and collaborating with cross...Work at officeRemote workWorldwide$79.5k - $158.5k
...Clinical Research Associate IIWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's... ...patients.Are you a motivated Clinical Research Associate with 2–3 years of monitoring experience who is looking for more than...Work at officeRemote workWorldwide$71.32 - $76.32 per hour
...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical... ...ISO 9001, ISO 14001, ISO 27001, and SOC 2 Type II standards, reflecting our...Temporary workLocal area$79.5k - $158.5k
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...Clinical Research Associate, Sponsor Dedicated Perform monitoring and site management work to ensure that sites are conducting the study(ies) and... ...recruitment plan. Minimum recruitment standards include 2.5 years of clinical research coordination experience at site...Full timePart timeImmediate startWorldwide$20.75 - $24 per hour
...Job Title: Research Technician Job Description... ...basic, translational, and clinical research studies. In this... ...At least 2 years of experience handling... ...therapeutic areas such as oncology, dermatology, orthopedics... ...positions located in the city and county of San Francisco...Permanent employmentContract workTemporary workMonday to FridayNight shiftWeekend workAfternoon shiftEarly shift$90.2k - $175.1k
IQVIA is now hiring for Clinical Research Associates located on the West Coast and East Coast, US to join our growing Early Clinical Development team working exclusively in Phase I.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team...Full timePart timeImmediate startWorldwide$90.2k - $175.1k
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional...Full timePart timeImmediate startWorldwide$87.2k - $169.3k
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...of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University...Work experience placement$64k - $189k
...IQVIA seeks an experienced Clinical Research Associate for sponsor-dedicated monitoring and site management across multiple U.S. regions. The role... ...enrollment, CRF completion and data queries Requirements ~2.5+ years clinical research coordination experience at site...- ...Senior Clinical Research Associate role focused on CNS and oncology studies at a global CRO. The position involves managing site activities across clinical trials, conducting study initiation visits, and ensuring regulatory compliance, primarily working remotely from...Contract workWork at officeRemote work
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...Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol... ...scientific or healthcare discipline preferred At least 2 years independent on-site monitoring experience as CRA...Work at office$74.5k - $197.5k
...IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple therapeutic... ...Healthcare, Nursing, or related field preferred Minimum 2 years of independent on-site monitoring experience in...Work at office- Job Title: Clinical Research Associate II (CRA II)Job Location: United States - RemoteJob Overview:The Clinical Research Associate II (CRA II) is responsible for monitoring assigned investigational sites throughout the clinical trial lifecycle. The CRA II serves as the...Interim roleWork at officeRemote work
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