Senior Clinical Research Associate - Site Monitoring Lead
Merck & Co.
Merck & Co. is seeking a Clinical Research Site Manager to oversee performance and regulatory compliance for assigned sites in the United States. The role acts as the primary site contact, ensures study conduct adheres to ICH/GCP guidelines, and drives site readiness and performance across multiple protocols. Responsibilities include developing site relationships, performing remote and on-site monitoring, and coordinating with sponsor teams to ensure data integrity, safety, and regulatory #J-18808-Ljbffr Merck & Co.
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Senior Clinical Research Associate - Oncology - Southern CaliforniaICON is a global healthcare intelligence... ...for performing investigative site management and monitoring activities throughout the... ...support site activation activities Lead site engagement initiatives and foster...SeniorWebsiteFull timeInterim roleLocal areaRemote work- ...term solutions. Position Purpose and Summary Interim housing sites run 24 hours a day, seven days a week. The quality of each shift depends a lot on who is leading it. The Lead Client Services Monitor (LCSM)holds the floor. Acting as a leader, collaborator, and an...WebsiteFull timeInterim roleImmediate startAll shiftsFlexible hoursShift workNight shiftAfternoon shift
$20.9 - $22 per hour
...benefits. JOB SUMMARY AND PURPOSE The Lead Monitor I will arrange, coordinate, and oversee... ...compliance of program rules, report to clinical/case management staff, assist clinical/... ...such as human service locations, work sites, and medical facilities Assists passengers...WebsiteHourly payWork at officeLocal areaShift work- ICON Strategic Solutions in Los Angeles seeks a Senior Clinical Research Associate specializing in Oncology. The role involves site management and monitoring activities during clinical trials to ensure data integrity and subject safety. The ideal candidate will have a Bachelor...SeniorWebsite
$110.52k - $138.15k
ICON in Los Angeles is seeking a Senior Clinical Research Associate specializing in Oncology. You will serve... ...contact between investigational sites and sponsors, ensuring compliance and... ...Life Sciences and 3+ years of on-site monitoring experience. The role offers a competitive...SeniorWebsite$140k - $165k
...Senior Clinical Research Associate - Remote PositionLocation: Los Angeles, CADepartment... ...her allocated investigative sites for all assigned clinical... .../Clinical Operation Lead/designee, to promote the efficient... ...the applicable Clinical Monitoring Plan (CMP), SOPs, and ICH...SeniorWebsiteFull timeInterim roleWork at officeRemote workWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud... ...for performing investigative site management and monitoring activities throughout the clinical...SeniorWebsiteWork experience placementInterim roleLocal areaRemote workFlexible hours- Hope the Mission seeks a Lead Client Services Monitor to guide on-site Client Service Monitors during graveyard shifts at Canoga Park, CA. You will lead the shift, perform wellness checks, ensure safety protocols, and maintain documentation and incident reporting with a...WebsiteShift workNight shift
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...currently seeking Senior Contract OncologyClinical Research Associate (SCRA) for an opportunity... ...Contract Oncology Clinical Research Associate... ...the Country for a leading Clinical Research... ...Conduct site and study visits and... ...perform all site monitoring activities across...SeniorWebsiteContract workRemote work$65 - $90 per hour
Overview C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Los Angeles... ...closely with investigative sites while ensuring high-quality execution... ...includes both remote monitoring and on-site visits, offering...SeniorWebsiteHourly payRemote work$82.08k - $123.12k
Arcadis is the world's leading company delivering sustainable design... ...a Lead Biological Compliance Monitor (Staff Environmental Scientist... ...accountabilities Under supervision of senior‑staff, support a regionally... ...Conducting field reviews and site visits with other technical...WebsiteFull timePart timeFor contractorsFor subcontractorWork at officeLocal area- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the... ...point of contact for investigative sites and sponsors, and providing... ...practical experience in medical research or clinical development. A minimum...SeniorWebsite
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - West Region ICON plc is a world-leading healthcare intelligence and clinical research organization... ...between investigational sites and the sponsor Conduct... ...selection, initiation, routine monitoring, and close-out Ensure site...SeniorWebsiteWork experience placementLocal areaVisa sponsorshipFlexible hours- ...Description Job Description The Senior Information Security Lead is a hands‐on senior... ...protection rules, and monitoring. Define and enforce network... ...where applicable). Research emerging threats and technologies... ...and is required to be on-site. \nCompany Description...SeniorWebsite
$19.5 per hour
...SOCC center is the main location for the monitoring and analysis of risks on a company scale... ..., cultivations, etc.) along with other associates while continuously auditing all locations... ...guards are positioned per each site's post orders. Performs work under direct...WebsiteHourly payFull timeLocal areaShift workNight shift$185k - $278k
...personnel gowning regimes, environmental monitoring, and the unique biological risks inherent... ...; provide cell therapy-specific input on site selection criteria, facility requirements... ...considerations ~ Provide input to and/or lead engineering studies to inform capital...SeniorWebsiteTemporary work$71.9k - $189k
IQVIA in Beverly Hills is looking for a Site Manager to oversee clinical studies. The role includes monitoring site compliance with study protocols and applicable regulations, conducting training, and ensuring effective communication with study sites. Candidates should...Website$70 - $75 per hour
...Sr. Field Clinical Research Associate Remote with Travel required in the North... ...THE ROLE Our client, a leading life sciences company, is seeking... ...role, you will be responsible for monitoring clinical studies at assigned sites to ensure compliance with regulatory...SeniorWebsiteHourly payContract workPart timeLocal areaRemote work- ...Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical research organization... ...medical device monitoring experience- however,... ...and identify issues at sites and implement effective...SeniorWebsiteRemote jobFlexible hours
- ...Senior CRA / CRA II - United States - Home... ...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’... ...on clinical trial monitoring tasks requiring technical... ...clinical trial sites to ensure... ...Clinical Research Associate, with a strong understanding...SeniorWebsiteRemote jobWork from homeFlexible hours
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...Position Overview Join a leading entertainment brand at the forefront... ...for presentation of research and analytics to client, with... ...Arbitron, ComScore), Paid Media Monitoring (e.g. Kantar, AdViews), Social... ...g. DART, Atlas, Mediamind) & Site Served, Website Analytics (e....SeniorWebsiteWork at officeLocal area- ...Responsibilities & Expectations The Senior Team Leader is an experienced... ...Protection Agent tasked with leading a team of at least 5-15... ...the trusted, senior most on-site leader. Scheduling, personnel... ...security of protectees Monitoring security systems and...SeniorWebsiteLocal areaShift workNight shift
$91.34k - $114.17k
Clinical Research Associate - Oncology - West RegionICON is a global healthcare intelligence and clinical... ...of contact between investigational sites and the sponsorConduct all types of... ...including selection, initiation, routine monitoring, and close-outEnsure site compliance...WebsiteFull timeLocal area$142.2k - $213.4k
...Manager (CAM) / Integrated Product Team (IPT) Lead based out of Woodland Hills, CA. As a... ...and navigation system. This role is on-site in Woodland Hills, CA. Responsibilities... ...solution development, implementation, and monitoring. Proven, effective planning, organizational...SeniorWebsiteContract workRelocation packageShift work$96.2k - $151.4k
...assigned protocols and sites in a country.Under... ...throughout all phases of a clinical research study, taking overall... ...as SME for monitoring processes and Systems... ...Monitoring Plan and associated documents.Gains an in... ...required.Supports and/or leads audit/inspection activities...WebsiteFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job... ...in the evaluation of potential clinical sites according to established criteria of... ...necessary materials. Conduct ongoing study monitoring, including frequent periodic site...WebsiteFull timeWork experience placement
- ...country where the job is located. Perform monitoring and site management work to ensure that sites... ...contracted scope of work and Good Clinical Practice.Work with sites to adapt, drive... ...skill in applying, applicable clinical research regulatory requirements. i.e., Good...WebsiteLocal area
- ...Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... ...will contribute to clinical trial monitoring activities, taking responsibility... ...responsibilities include: Conducting site qualification, initiation,...WebsiteFlexible hours
$80k - $130k
What This Is You own IVD diagnostic clinical studies end-to-end — site activation through data lock — across multiple active trials at once. You are not a monitor who writes reports. You are the person who makes studies move. The Culture RDI runs sample collection studies...SeniorWebsite
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