Study CRA
$71.9k - $145.3kIQVIA
A leading global provider of advanced analytics is looking for Study Start-Up Clinical Research Associates to join their team. The role involves site selection and start-up activities for Phase I-IV trials across the United States. Candidates should have at least 6 months of monitoring experience and strong knowledge of ICH/GCP regulations. The position offers a competitive salary range of $71,900 to $145,300, depending on qualifications and location. #J-18808-Ljbffr
- ...CRA 2/Senior CRA Carlsbad, United States of America | Full time | Field-based | R1547446 Join a team that's advancing clinical... ...partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus....SuggestedFull time
$71.9k - $145.3k
...IQVIA Argentina is looking for a Study Start-Up Clinical Research Associate in Carlsbad, USA. This full-time, field-based position requires experience in Study Start-Up and at least 6 months of monitoring experience. The role involves managing site selections, ensuring...SuggestedFull time$71.9k - $169.3k
...IQVIA is seeking a Site Manager in Carlsbad, California to oversee study site management and monitoring activities. This role involves conducting site visits, ensuring adherence to regulatory guidelines, and maintaining communication with study sites. A Bachelor's degree...Suggested- ...in surgical procedures, dosing, and sampling techniques will be crucial to facilitate protocol development and enhance preclinical studies. Primary Responsibilities: This position requires a broad knowledge of the anatomy and physiology of small and large animals...SuggestedTemporary workWorldwideFlexible hours
$71.9k - $119.9k
...IQVIA Argentina is seeking a Clinical Research Associate I (CRA I) based in Carlsbad, California. This full-time role involves supporting clinical research studies through site monitoring and management activities. Key responsibilities include conducting monitoring visits...SuggestedFull time$71.9k - $169.3k
...Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring...Full timePart timeLocal area$87.2k - $169.3k
...looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality... ...with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus....Full timePart timeImmediate startWorldwide$71.9k - $119.9k
...IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology... ...role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In...Full timePart timeImmediate startWorldwide$69.8k - $226.8k
...A leading clinical research organization seeks a Clinical Research Associate to manage study sites, ensure adherence to protocols, and enhance recruitment efforts. Ideal candidates will have at least 2.5 years of monitoring experience, preferably in oncology or immunology...Full time$71.9k - $169.3k
...Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform...Full timePart timeLocal areaImmediate startWorldwide- ...IQVIA Argentina is hiring a Clinical Research Associate (CRA) based in Carlsbad, California. This role focuses on monitoring clinical sites to ensure compliance with study protocols and regulatory requirements. The ideal candidate will have at least a Bachelor's degree...
- ...IQVIA is looking for a Clinical Research Associate (CRA) in Carlsbad, California, to lead various clinical trials and ensure high-quality study execution. The successful candidate will monitor sites, manage study progress, and will have a significant impact on improving...
$87.2k - $169.3k
...IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring experience in oncology. IQVIA Biotech... ...and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol,...Full timePart timeLocal areaImmediate startWorldwide$87.2k - $169.3k
...clinical research company is hiring a Senior Clinical Research Associate in Carlsbad, CA. The CRA will be responsible for monitoring clinical sites and ensuring compliance with study protocols and regulations. Ideal candidates should possess at least 1.5 years of on-site...$71.9k - $189k
...IQVIA LLC in Carlsbad, CA is seeking a Clinical Research Associate to ensure sites conduct studies according to protocols and regulations. This role involves monitoring sites, managing study progress, and maintaining documentation. Candidates must possess a Bachelor's...- ...dedicated to sponsor projects based in Carlsbad, California. The role involves monitoring site activities and ensuring compliance with study protocols and regulations. Suitable candidates should possess at least 1.5 years of on-site monitoring experience and a Bachelor’s...
$71.9k - $189k
...a Clinical Research Associate! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients...Full timePart timeWork at officeLocal areaImmediate startWorldwide$87.2k - $169.3k
IQVIA Argentina in Carlsbad seeks a Senior Clinical Research Associate to ensure successful clinical trial execution. Responsibilities include monitoring clinical sites, conducting site visits, and ensuring compliance with protocols. Ideal candidates should have at least...$71.9k - $145.3k
...Study Start-Up Clinical Research Associate, Sponsor Dedicated Carlsbad, United States of America | Full time | Field-based | R1513886 IQVIA... ...anywhere in the United States. Job Overview The Study Start-Up CRA is accountable for site selections as well as study-specific...Full timePart timeLocal areaImmediate start- ...and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol,... ...in lieu of degree./liliSome organizations require completion of CRA training program or prior monitoring experience./liliBasic knowledge...Full timeLocal area
- ...540070/ppIQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety... ...monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your...Full time
$27 - $33 per hour
...Position: Study Coordinator Location: Carlsbad, CA (on-site) Hourly Range: $27.00 - $33.00 Job Overview The Study Coordinator plays a critical role in supporting and coordinating preclinical in vivo studies, with a focus on cell and gene therapy (CGT) programs. This individual...Hourly payTemporary workFlexible hours$25 - $32 per hour
...Animal Research Associate I/II, In-vivo studies (Contract to Hire) Looking to hone your animal surgery skills? One of San Diego’s leading biotech companies is looking for a competent, reliable Research Associate to add to their dynamic team. This role offers the opportunity...Hourly payContract work- ...Pharmaron in Carlsbad, CA is hiring a Study Coordinator to support and coordinate preclinical in vivo studies with a focus on cell and gene therapy programs. Responsibilities include coordinating study activities, ensuring data integrity, and compliance with regulatory...
- Profound Research is looking for a Clinical Research Coordinator to manage clinical trial activities in Carlsbad, California. Responsibilities include conducting trials according to established protocols, mentoring staff, and ensuring compliance with regulations. Candidates...Remote work
- ...Senior Scientist for CGT Preclinical to drive innovative research in cell and gene therapy. The ideal candidate will lead in vivo studies, ensuring compliance and operational efficiency while collaborating with internal teams and external sponsors. A Ph.D. in a relevant...
$22 - $29.91 per hour
...attending and participating in civic and community events for the purpose of generating additional business and identifying potential CRA opportunities for the Bank. Engage in sales practices that are aligned to create value for both the customer and the bank....Hourly payWork at officeImmediate startShift work$70.3k - $105.4k
...Bachelor's plus 5 years of sales experience, preferably in laboratory, scientific, or healthcare industries Preferred Fields of Study: Life Sciences, Chemistry, Biology or related scientific field Technical knowledge and ability to understand customer applications...Temporary work$144k
...diagnostic units. Performs imaging of the head, neck, spine, chest, and body. The purpose of these exams is to conduct diagnostic studies to bring about proper diagnosis and treatment. The duties associated with this position include, but are not limited to, the following...Full timeWork experience placementImmediate startRemote workMonday to FridayShift work$2,000 - $2,500 per month
...largest providers of private practice internships and residencies in the U.S. Opportunities to participate in a robust clinical studies program Additional Benefits ~ Up to 100% Pet Care Discount for your own pets ~100% paid professional liability coverage ~1...Full timeTemporary workLocumInternshipPrivate practiceLocal areaShift workNight shiftDay shift
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