- Parexel (Little Rock, AR)
- The Senior Clinical Research Associate ( Sr . CRA ) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management...the set-up, running and close-out of sites in a clinical trial . Monitoring Responsibilities and… more
- ThermoFisher Scientific (Suwanee, GA)
- …within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical...Fisher Scientific in the Republic of Georgia, is hiring Senior CRA on full-time permanent position. This… more
- BeOne Medicines (San Mateo, CA)
- …of relevant Clinical Operations experience Minimum of 3-4 years of ( CRA ) monitoring experience in the pharmaceutical or CRO Industry Excellent communication ... the job: Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs...data collection is met per contractual guidelines Works with Clinical Trial Oversight Managers (CTOMs) and … more
- Edwards Lifesciences (Kansas City, KS)
- …need (Required): Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring , with a strong focus on quality assurance, ... in cardiology Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) Prior clinical research experience… more
- Kaiser Permanente (Oakland, CA)
- …standard contracts or agreements (eg, subawards, subcontracts, data use agreements, clinical trial agreements); reviewing, editing, and providing consultation to ... and compliance documentation to meet government and funding agency requirements; monitoring and validating data in enterprise-wide research administration… more
- Parexel (Atlanta, GA)
- The Senior Clinical Research Associate ( Sr . CRA ) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management...the set-up, running and close-out of sites in a clinical trial . ** Monitoring Responsibilities and… more
- ICON Clinical Research (TX)
- …shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate ( CRA ) to join our diverse and dynamic ... Senior Clinical Research Associate ICON...team. As a Senior CRA at ICON Plc, you will...the study lifecycle. **What You Will Be Doing:** + Monitoring clinical trial sites to… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …discipline. * 6+ years' experience as a Clinical Research Associate . * Extensive knowledge of trial oversight activities, GCP/ICH and federal ... Sr CRA will be responsible for monitoring clinical studies at the site level...needs of the organization._ **Job Locations** _US-IL-Chicago_ **Title** _Senior Clinical Research Associate ( CRA… more
- Abbott (Alameda, CA)
- …**The Opportunity** The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical ... senior staff in development of study-specific forms and trial -specific monitoring plans. + Assist senior...preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate… more
- Parexel (Juneau, AK)
- **Job Purpose:** The Senior Clinical Research Associate I ( Sr . CRA ) is responsible for the site management, site monitoring and close-out of ... Clinical Practices (GCP), and sponsor standards. The Sr . CRA is accountable for site management...and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities… more
- BeOne Medicines (San Mateo, CA)
- …across clinical trial operations. Minimum 2 years of experience in clinical trial monitoring or direct study management + Minimum 2 years ... required. + Experience in clinical operations as clinical research associate , clinical...(eg, Clinical Operations, Clinical Compliance, Clinical Monitoring , Clinical Trial… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites ... we'd love to hear from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- ICON Clinical Research (Blue Bell, PA)
- …of clinical development. ICON plc is seeking an experienced Senior Clinical Research Associate ( Senior CRA ) or Clinical Research ... 1 year of independent monitoring experience for CRA II consideration and 3 years for Senior...Senior CRA . + Strong knowledge of clinical trial processes, regulatory requirements, and ICH-GCP… more
- ICON Clinical Research (PA)
- … II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate . + In-depth knowledge of clinical ... Senior CRA / CRA II ICON plc is a...future of clinical development. We are currently seeking a Senior Clinical Research Associate or … more
- ThermoFisher Scientific (West Hills, CA)
- …abilities to perform the job (comparable to 10 Months - 2 years as traveling clinical research associate ). Valid driver's license where applicable. In some ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical... portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver… more
- ThermoFisher Scientific (Suwanee, GA)
- …within our PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical...Fisher Scientific in the Republic of Georgia, is hiring Senior CRA on full-time permanent position. This… more
- BeOne Medicines (Emeryville, CA)
- …**Essential Functions of the job:** * Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the ... collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and ... Operations experience * Minimum of 3-4 years of ( CRA ) monitoring experience in the pharmaceutical or… more
- ThermoFisher Scientific (Chicago, IL)
- …weather conditions **Job Description** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site ... as required. Ensures study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of reports generated… more
- ARTIDIS (Houston, TX)
- …are unique, the clinical studies are designed and supervised directly by ARTIDIS. The Senior Clinical Research Associate (SCRA) is an integral part ... clinical studies. SCRAs work hand in hand with Clinical Quality Development, Clinical Research ...in ARTIDIS's study sites globally, providing specific oversight on clinical study monitoring activities, clinical … more
- Olympus Corporation of the Americas (Center Valley, PA)
- …study data, including facilitating the resolution of data queries under the guidance of the Clinical Research Associate ( CRA ), Data Management and/or the ... about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr . Clinical Trial Coordinator (...Minimum of two (2) or more years experience in clinical research , with medical device and/or pharmaceutical… more
