Clinical Research Monitor — Site & Data Oversight
$71.9k - $169.3kItlearn360
Itlearn360 is hiring a Clinical Research Associate in Parsippany-Troy Hills, NJ. The role involves monitoring and managing study sites, ensuring adherence to study protocols and regulations. Candidates should have a Bachelor’s degree in a scientific discipline and at least one year of on-site monitoring experience. The job offers a base pay range of $71,900 to $169,300 annually, depending on qualifications and location. #J-18808-Ljbffr Itlearn360
- ...Director Medical Monitor Location: Parsippany,... ...onsite Provide medical oversight for assigned clinical studies from study... ...and study sites regarding protocol-related... ...review of subject safety data, eligibility determinations... ...of clinical research, ICH-GCP, FDA, EMA, and...DataWebsiteFor contractorsLocal area
$87.2k - $182k
IQVIA is looking for a Site Manager in Parsippany-Troy Hills, NJ. The role requires performing monitoring visits and managing site data to ensure compliance with study protocols and regulations. Ideal candidates will hold a Bachelor’s degree in a scientific field and possess...DataWebsiteWork at office$108.5k - $201.5k
Novartis Group Companies is looking for a Senior Clinical Research Associate (CRA) to perform site monitoring activities related to clinical trials. This remote position... ...with protocols while providing high-quality data. The ideal candidate will have at least 3 years of...DataWebsiteRemote job$47.4k - $169.3k
IQVIA Argentina in Parsippany, New Jersey is seeking a Clinical Research Associate. The role involves performing monitoring and site management work to ensure compliance with study protocols and regulations. Candidates should have a Bachelor's degree in a scientific discipline...Website$47.4k - $169.3k
IQVIA is seeking a site monitor for clinical studies in Parsippany-Troy Hills, NJ. The role involves performing monitoring visits, managing site practices, and ensuring adherence to regulatory guidelines. Qualifications include a Bachelor's degree in a scientific discipline...Website- ...Argentina is seeking a dedicated individual for a full-time position in Parsippany, United States, focused on site monitoring and management within clinical research. You will conduct site visits, ensure adherence to study protocols, and evaluate site practices in...WebsiteFull time
- A leading clinical research organization seeks a Clinical Research Site Manager in Parsippany-Troy Hills, NJ. This role involves conducting site monitoring, developing recruitment plans, and providing protocol training. Candidates must have a BS degree and at least 2.5...WebsiteWork at office
$71.9k - $189k
Dormont Manufacturing Co is seeking a Site Monitor in Parsippany-Troy Hills, NJ. The role involves... ...compliance, and managing study data integrity. The ideal candidate will have... ...monitoring experience. Strong knowledge of clinical research guidelines is a must. This position...DataWebsite$25 - $39 per hour
IQVIA LLC is looking for a Spanish Bilingual Site Research Assistant to support clinical trial activities in Parsippany-Troy Hills, NJ. In this role, you will perform EDC data entry, assist in recruiting participants, and ensure compliance with protocols while maintaining...DataWebsiteHourly pay$182k - $346k
...Clinical Research Director AbbVie's mission is to discover and deliver... ...high-quality clinical data supporting overall... ...of investigators, study site personnel, and AbbVie study... ...overall responsibility for oversight of clinical studies, monitoring overall study integrity,...DataWebsiteWork at officeImmediate startRemote workMonday to Friday- ...We are seeking an experienced Clinical Research Specialist to support clinical studies and product... ...initiatives and study execution. Conduct data review, validation, statistical analysis... ...and support of investigational study sites and external stakeholders. Participate in...DataWebsiteRemote work
- ...specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.... ...content within departmental SharePoint site. • Maintain monthly and High Priority... ...absence. KEY CRITERIA: Finance Background. Data Systems Management. Experience with...DataWebsiteContract work
$64k - $189k
...Clinical Research Coordinator 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. Position requires...DataWebsiteFull timePart timeLocal areaImmediate startWorldwide$87.2k - $145.3k
...minimum of 1.5 years of on-site oncology monitoring experience: Essential Functions... ...requirements, i.e., Good Clinical Practice (GCP) and... ...completion and submission, and data query generation and resolution... ...provider of clinical research services, commercial insights...DataWebsiteFull timePart timeLocal areaImmediate startWorldwide- ...performing study specific clinical and regulatory... ...recruit subjects to collect data from patient charts, medical... ...or inconsistencies and monitors patients' progress to... ...and the application of research techniques, assists in... .... Our facilities and sites of care include:...DataWebsiteHourly payFull timeTemporary workPart timeFor contractorsFor subcontractorFlexible hours
$127.28k - $190.92k
...Description Job Title: Manager, Clinical Adjudication Operations... ...can support clinical research studies in all phases.... ...review to assure data completeness, consistency... ...Documentation Provide oversight of the creation and... ...filing of Charters, Plans, Site Manuals, Quick...DataWebsite$40 - $60 per hour
Overview The Contract Clinical Trial Associate (CTA), Clinical... ...of potential clinical sites; maintain investigator lists... ...), queries and clinical data flow Utilize JDE system to monitor funds on existing... ...knowledge of applicable clinical research regulatory requirements...DataWebsiteHourly payContract workWork experience placementLocal area$71.9k - $169.3k
Clinical Research Associate — Sponsor Dedicated — IQVIA, Parsippany Troy Hills, NJ. 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...DataWebsiteLocal area- ...community volunteer and employment sites, group homes or apartment... ...while also conducting direct clinical work. Responsibilities The... .... Engages in ongoing data review and analysis to ensure... ...IDT). Conducts and presents research to internal and external audiences...DataWebsiteFull timeTemporary work
$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you'll play a crucial role... ...requirements. Essential Functions Site Monitoring: Conduct selection, initiation,... ...report form (CRF) completion, and data query resolution. Support the start-up...DataWebsiteFull timePart timeLocal areaImmediate startWorldwide$75k - $95k
...practices for image capture, analysis, and data interpretation Provide image analysis... ...clear, actionable insights that support clinical, research, and business decision‑making Act as a... ...Willingness to travel to conferences and customer sites Desired Photography or imaging domain...DataWebsiteFull timeWork at office$136.08k - $204.12k
Clinical Study Manager, Clinical Operations Job Summary The... ...Responsibilities Study Oversight: Lead the clinical study... ...materials are in place. Data Cleaning: Oversee site and monitor data cleaning metrics including... ...clinical or basic research in a Pharmaceutical company...DataWebsiteContract workWork at office- ...search behavior Define and validate structured data requirements including schema markups and... ...internal linking structures Support off-site backlink strategies by ensuring technical... ...team and web development partners Monitor performance (ranking, position, keywords)...DataWebsiteLocal area
$105k - $145k
...currently seeking a Companion Animal Clinical Development Clinician to join... ...and study conduct to research and development phase projects... ...management Investigator and site selection Protocol development and writing Study monitoring Data analysis and interpretation...DataWebsiteFull timeTemporary workPrivate practiceLocal area$47.4k - $169.3k
Clinical Research Associate, Full Service Parsippany, United States of America | Full time |... ...based | R1497311 Job Overview Perform monitoring and site management work to ensure that sites... ...the study(ies) and reporting study data as required by the study protocol, applicable...DataWebsiteFull timeLocal areaImmediate start$62.3k - $237.7k
...Site Enrollment and Engagement Lead - Licensed Medical Professionals... ...information and education on clinical trial inclusion and exclusion... ...s degree (minimum) Clinical research experience Active license... ...outreach, chart reviews, and data abstraction ~ Ability to work...DataWebsiteFull timePart timeImmediate startWorldwideNight shift- ...Group Eligibility Liaison to leverage scientific expertise in clinical research. In this role, you will coordinate and manage communication between clinical sites and the review group, ensuring timely data delivery and participant readiness for eligibility review. Your...DataWebsite
- ...manage field survey operations with minimal oversight Perform boundary surveys, topographic... ...robotic total stations, GPS/RTK systems, and data collectors Interpret plans, perform field calculations, and solve problems on-site Produce accurate field notes, sketches,...DataWebsiteWork at officeRemote workNight shift
- ...DESCRIPTION The Oncology Data Coordinator is... ...reporting, and quality oversight of clinical and registry data for... ...Blood & Marrow Transplant Research (CIBMTR), FACT/JACIE accreditation... ...documentation. Monitor data discrepancies,... ...Leave Backup and On‑Site Childcare Well‑Being...DataWebsiteFull timeTemporary workPart timeFor contractorsFor subcontractorFlexible hours
$206.5k - $393k
...Clinical Development Program Lead Leads the direction... ...of clinical trials or research activities of one or more... ...high-quality clinical data supporting overall... ...of investigators, study site personnel, and AbbVie study... ...clinical study teams, monitoring overall study integrity...DataWebsiteWork at officeImmediate startRemote workMonday to Friday
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