Clinical Research Associate I — Site Monitoring
Syneos Health, Inc.
Syneos Health, Inc. in Morrisville, NC is seeking a CRA I to support site monitoring activities across sponsor studies. You’ll perform site qualification, initiation, monitoring and close-out visits, on-site or remotely, ensuring ICH-GCP compliance and accurate data capture. Travel up to 75% is required; strong organizational and communication skills are essential. Requirements include a Bachelor’s degree or RN, knowledge of GCP, willingness to learn, and the ability to work across teams. #J-18808-Ljbffr Syneos Health, Inc.
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...Clinical Research Associate- West Coast At ICON Strategic Solutions, you will work in a sponsor-dedicated... ...involve delivering clinical trial monitoring work to a high standard, working... ...stakeholders, clinical investigators, and site staff. Ensure patient safety by...WebsiteWorldwideFlexible hours- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical... ...belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
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...Id: 0000177692Job Category: Clinical ResearchJob Location: Raleigh... ...actively seeking Clinical Research Associates II to join a top-tier CRO with... ...bridge between sponsors and sites, ensuring clinical trials... ...collaboratively with the team to ensure monitoring activities meet study...WebsiteRemote work$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... ...partner with investigative sites and cross-functional teams to... ...’ll DoLead and execute site monitoring visits (selection,...WebsiteFull timePart timeImmediate startWorldwide$90.2k - $197.5k
Position Summary The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating... ...activities involved in initiating, monitoring, and completing clinical research... ...of clinical studies including site selection, study initiation, site monitoring...WebsiteFull timePart timeImmediate startWorldwide$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... .... In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols,...WebsiteFull timePart timeImmediate startWorldwide$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing... ...Visits: Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance...WebsiteFull timePart timeWork at officeLocal areaImmediate startWorldwide$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates... ...are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a... ..., you will be responsible for monitoring and managing clinical sites to ensure compliance with study...WebsiteFull timePart timeImmediate startWorldwide- ...quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an... ...training curricula) in hematology/oncology monitoring, which includes a general cancer overview... ..., and closeout visits at research sites in compliance with the approved protocolCommunication...WebsiteContract workWork at officeRemote workWork from home
- ...Senior Clinical Research Associate - Oncology (US) Location: Durham, NC area. Employer type: CRO (San Antonio site). What the work involves: Our mission is to work with passion... ...processes. Conduct all types of monitoring visits: Pre-Site Selection Visits (...WebsiteContract workInterim role
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...Make an Impact as a Clinical Research Associate II at Worldwide As a Clinical Research Associate II... ...research by partnering with investigative sites and study teams throughout the study... ...of site qualification, initiation, monitoring, management, and close-out activities...WebsiteHourly payWork at officeLocal areaWork from homeWorldwide$74.5k - $197.5k
...Clinical Research Associate II IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas: Central Nervous System...WebsiteFull timePart timeWork at officeImmediate startWorldwide$65 - $72 per hour
Job Overview:The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical... ...as well as some travel to conduct site visits or to attend client or internal... ...position candidates complete the Fortrea Monitoring Excellence Academy (MEA) training...WebsiteWork at officeLocal areaRemote workWork from home$55.86 - $62.07 per hour
...Sr Clinical Research Associate I Kelly Science and Clinical is hiring on behalf of one of our large CRO clients to support... ...future extension. We are looking for strong CRA monitors to support regional studies at sites across the East Coast. The ideal candidate will have...WebsiteHourly payFull timeContract workWork at officeRemote workHome officeFlexible hours$50k - $99k
**What the In-House Clinical Research Associate II does at Worldwide Clinical Trials:**The experienced... ...Associate II (IHCRA) is responsible for site management tasks for studies in... ...study initiation, interim and remote monitoring, and close-out visits under the guidance...WebsiteHourly payInterim roleWork at officeLocal areaRemote workWorldwide
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