- University of Colorado (Aurora, CO)
- Clinical Research Monitor I - 34812...and financial goals. + May provide regulatory support for clinical trials , including QA/QC reviews, submissions to ... Clinical Research Support Team (CReST)** **Job Title: Clinical Research Monitor I** **Position #: 827305...Clinical Practices Manual, FDA Regulations in relation to clinical trials , NIH guidelines, ICH guidelines and… more
- ThermoFisher Scientific (Cambridge, MA)
- …on the job. Minimum Qualifications * Minimum of 2 years of experience with clinical trials /medical research required.as a Clinical Research Associate (CRA) ... * Bachelor's degree in related field. * Experience with quality assurance or clinical trial auditing/monitoring, and/or good clinical practice. * Thorough… more
- UTMB Health (Galveston, TX)
- …studies approved by UTMB Institutional Review Board (IRB). Ensures the safety of clinical trial participants and maintains the accuracy and integrity of ... Clinical Study Monitor (IRB) - Provost...trial data. **Preferred Experience:** Two years of previous clinical trial monitoring experience preferred. **Job Duties:**… more
- Pennsylvania State University (Hershey, PA)
- …at the Penn State College of Medicine, Hershey, PA, is hiring a full-time Clinical Trial Research Monitor . The Beat Childhood Cancer Research Consortium ... Beat Childhood Cancer (beatcc.org) (https://research.beatcc.org/) Job Duties & Responsibilities: The Clinical Trial Research Monitor is primarily responsible… more
- University of Southern California (San Diego, CA)
- …advancing the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials . Incumbent will provide oversight to the progress of ... clinical trials at study sites, and ensure...clinical trials at study sites, and ensure that they are...study protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance… more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials . Monitor staffing levels, and identify adequate ... strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials . Develop consent forms for approval by Human… more
- Morehouse School Of Medicine (Atlanta, GA)
- …for staff handling research administration activities associated with the conducting of clinical trials . Monitor staffing levels and identify adequate ... strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials . Develop consent forms for approval by Human… more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials . Monitor staffing levels, and identify adequate ... strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials . Develop consent forms for approval by Human… more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials . Monitor staffing levels and identify adequate ... strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials . Develop consent forms for approval by Human… more
- ThermoFisher Scientific (Columbus, OH)
- …a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of ... research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver... clinical research services provide end-to-end support for clinical trials from study start up to… more
- Bristol Myers Squibb (Princeton, NJ)
- …assigned project to execute activities associated with the conduct + May serve as Clinical Trial Lead for one or more trials + May lead or support trial ... Will be responsible for design and execution of assigned clinical trial activities and work closely with...present these at SIVs and Investigator meetings + Review clinical narratives + Monitor clinical … more
- Emory Healthcare/Emory University (Atlanta, GA)
- …throughout the course of the research projects. + Clinical Monitoring: Monitor participants' progress throughout the trials , and promptly report any adverse ... + Coordinate and provide logistics support for patient appointments related to the trial . + Inform and coordinate available resources at Grady and within the… more
- Touro University (Hawthorne, NY)
- Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... other multi-institutional protocols. + Screen and enroll patients onto clinical trials in collaboration with clinical...with the Good Clinical Practice guidelines in clinical research. + Monitor study patients for… more
- Mayo Clinic (Jacksonville, FL)
- …state, sponsor, and institutional guidelines. The CDA I provides data management support for clinical trials . The CDA I is responsible for data collection in a ... sponsors or CRO personnel. The CDA I is responsible for scheduling clinical research monitor visits, maintaining the monitor visit calendar, and serving as… more
- Walgreens (Deerfield, IL)
- …to provide medical oversight and leadership serving as Principal Investigator and Medical Monitor for clinical trials on behalf of Pharmaceutical (Sponsor) ... **Job Description:** **Job Summary** Walgreens RWE Clinical Trials is seeking an experienced...Business Leadership** + Provides medical and scientific leadership for clinical trial design, protocol development, and execution… more
- TE Connectivity (Los Angeles, CA)
- …As needed, provide administrative support to other CRAs. **Responsibilities:** + Implement and monitor clinical trials , with minimal oversight, to ensure ... studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported...other contractual obligations + Review and verify accuracy of clinical trial data collected, either onsite or… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate, you will monitor clinical trial programs and manage regional clinical trial sites to support biological ... Travels up to 80% within an assigned territory, monitors clinical trials according to monitoring plans to...Manager. + Internal support is provided to the Field Monitor from the assigned Clinical Trial… more
- Bristol Myers Squibb (Madison, NJ)
- …and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials + Successfully leads, plans, and executes ... implementation all study startup/conduct/close-out activities as applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical … more
- WuXi AppTec (Austin, TX)
- …time and within budget. The Senior CRA will work to manage, oversee and may monitor /co- monitor clinical trial sites. **Essential Job Functions:** + ... and is assigned as a study lead to manage clinical trial studies. The Senior CRA will...with a Project Manager to support activities on complex/larger trials and will work collaboratively with internal and external… more
- Kelly Services (South San Francisco, CA)
- …**KEY RESPONSIBILITIES** Clinical Trial Management: + Oversee and monitor clinical trial activities at investigative sites, ensuring compliance ... + Google Cloud Platform (GCP) + Good Clinical Practice (GCP) + Clinical Trials + SharePoint + Trial Management + Industry standards + Clinical… more