Average salary: $119,151 /yearly
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$110.52k - $138.15k
...Sr. CRA - Phase 1 Oncology West Coast At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development...SuggestedRemote jobWorldwideFlexible hours$72k - $145k
...suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc). • Facilitates effective communication between investigative sites, the client company and the PPD project team...SuggestedRemote jobFull timeTemporary workWork at officeHome officeFlexible hoursNight shift- Senior Clinical Research Associate position supporting oncology trials across investigational sites in a remote capacity. Responsibilities include risk-based monitoring, protocol compliance assessment, data quality review, and site management to ensure regulatory adherence...SuggestedRemote work
- ...individuals to help drive industry-leading innovation, With Heart®. About the Role We are seeking a Clinical Research Associate (CRA) with Ophthalmology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through...SuggestedFull timeWork at officeWorldwideFlexible hours
$81k - $114k
...participate in events that support the Bank's mission to provide education and services to all communities in our service area, as required by CRA. Minimum Qualifications to Perform Essential Functions Knowledge, Skills and Abilities: Effective team leadership and training...SuggestedFull time- ...manages essential documentation, and applies risk-based monitoring principles to ensure high-quality data and participant safety. The Sr CRA I acts as a site process specialist, ensuring that each trial is conducted in accordance with the approved protocol, ICH-GCP...SuggestedContract workWork at officeRemote workWork from homeFlexible hoursNight shift
$120k - $252k
...cybersecurity, or equivalent experience Deep understanding of cybersecurity frameworks and EMEA regulations, such as NIST-CSF, RED, CRA, NIS2, CAF, SOC2, ISO 27001 Knowledge of cyber security standards e.g. IEC 62443, UL 2900, ETSI EN 303 645, EN 18031, EN 40000. Certified...SuggestedHourly payFull timeTemporary workFlexible hours$86k - $128k
...medical device and/or in vitro diagnostic clinical studies; pharmaceutical clinical research experience will also be considered. CRA or clinical research certification (e.g., CCRA, CCRC, or CCRP). Current GCP certification. Clinical research or healthcare experience...SuggestedTemporary workFor contractorsWork experience placementWork at officeFlexible hoursShift work$65 - $90 per hour
...and scientific integrity, and we welcome individuals who take pride in contributing to well-run clinical trials. If you are a Senior CRA based in the greater San Diego area with strong CNS monitoring experience and are interested in working within a collaborative...SuggestedHourly payRemote work$74.1k - $148.3k
...there has never been a more exciting time to join us! As a global leader we're looking for a Senior Lead Clinical Research Associate (CRA) to drive success as part of our Non-interventional Study team. Join Oracle as a Lead CRA and make a real impact by guiding teams,...SuggestedFull timeContract workTemporary workFlexible hours- ...Vice President, Banking Compliance, HMDA & CRA Officer About the Company A growing bank strengthening its compliance program across deposit operations and lending. Industry Banking Type Privately Held About the Role The Company is in search of a...Suggested
- ICON Strategic Solutions is looking for a Senior Clinical Research Associate in Los Angeles. This role involves serving as the primary contact between investigational sites and the sponsor, ensuring compliance, and conducting various site visits. The ideal candidate will...SuggestedFlexible hours
$71.9k - $169.3k
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be located anywhere in the US. Job Overview...SuggestedFull timePart timeLocal area$58.62 - $62.07 per hour
...manages essential documentation, and applies risk-based monitoring principles to ensure high-quality data and participant safety. The Sr CRA I acts as a site process specialist, ensuring that each trial is conducted in accordance with the approved protocol, ICH-GCP...SuggestedContract workTemporary workWork at officeRemote workWork from homeFlexible hoursNight shift$63.5 - $64.9 per hour
...month renewable) ALL TRAVEL HOURS PAID (door to door) benefits provided Job Title: Senior Clinical Research Associate II (Sr CRA II) Job Description This Senior Clinical Research Associate II role focuses on performing and coordinating all aspects of...SuggestedContract workTemporary workWork at officeRemote workWork from homeHome officeFlexible hours- ...Job Description Job Description Job Title: Sr CRA (Level I) Location: Remote (Only West coast candidate) Duration: 6 Months Job Description: This is a request for a Sr. CRA I located in the "West" US- not required to be in Henderson, NV- can be hired from...Work at officeRemote workFlexible hours
$90 - $96 per hour
...Nervous System (CNS) domain. This hybrid role is primarily home-based, with regular on-site visits to assigned research sites. The Senior CRA ensures that studies comply with Good Clinical Practices (GCP), local and international regulations, and Standard Operating...Contract workTemporary workInterim roleLocal areaImmediate startRemote workWork from home$24 - $38 per hour
...Job Description Location to be within Plumas Bank's geographical footprint and based on applications received. The Compliance & CRA Specialist supports the Bank’s Compliance Management System and CRA Program through compliance monitoring and testing, marketing reviews...$110.52k - $138.15k
...Associate position overseeing clinical trial monitoring activities across multiple sites in Southern California. The role requires extensive CRA experience, strong regulatory knowledge, and the ability to lead teams while ensuring protocol adherence and data integrity....$74.5k - $175.1k
IQVIA seeks a Clinical Research Associate to conduct site monitoring and management for clinical studies. The role ensures sites comply with protocols, regulations, and sponsor requirements while managing recruitment, data quality, and study documentation. Responsibilities...Work at office$110.52k - $138.15k
...collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory...Full timeWorldwide- ...grow beyond limits, you'll feel right at home here. Daily Responsibilities: Draft the technical roadmap and execution plan for CRA compliance and adjust it as requirements evolve. Translate regulatory requirements into concrete technical proposals: what the platform...Immediate start
$87k - $123k
...to 75% domestically. What else we look for (Preferred): Clinical research certification (ACRP or SoCRA clinical coordinator / CRA certification) Strong written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills...Full timeWork experience placement$90.2k - $175.1k
IQVIA seeks a Senior Clinical Research Associate with experience in therapeutic areas including oncology, cardiovascular, or metabolic disease. The role involves site monitoring, protocol management, and regulatory oversight for clinical trials across multiple locations...$90.2k - $150.4k
...completion, and data queries Requirements ~ Bachelor's degree, preferably in scientific or healthcare discipline ~1.5 to 2 years of CRA experience including on-site monitoring ~ Knowledge of Good Clinical Practice (GCP) and ICH guidelines ~ Experience with protocol...$105.1k - $197.5k
IQVIA Biotech seeks an experienced Senior Clinical Research Associate to manage and monitor oncology clinical trial sites. The role involves ensuring protocol compliance, conducting site visits, supporting patient recruitment, and collaborating with cross-functional teams...Work at office$100k - $112k
...Our FSP team is currently seeking experienced Oncology CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical...Full timeWork at officeLocal areaRemote workNight shift- ...surprise our customers, i.e., doing something above and beyond their expectations that makes them feel special Minimum of 10 hours CRA volunteer hours per year. Volunteer hours are typically scheduled within business hours. This is compensable time and mileage is...
$130.4k - $179k
...reviews, penetration-test remediation, and security assessments. Support security requirements related to PCI, EU RED/EN 18031, EU CRA, ETSI EN 303 645, NIST, and OWASP. Develop security metrics and provide technical reporting on vulnerabilities, remediation,...Full time$90k - $150k
...Thrives in collaborative, cross-unit environments emphasizing transparency and reliable follow-through Participate in community and CRA activities to promote the Company's brand in our communities. Other Responsibilities Successfully complete all mandatory...Work at office
