- IQVIA (Durham, NC)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (San Diego, CA)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Overland Park, KS)
- **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved ... Skills and Knowledge Requirements** + ≥2 years of experience as a Clinical Research Associate , with specific in vitro diagnostics study experience +… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Caris Life Sciences (Boston, MA)
- …Communicate effectively with the research team, investigator(s), Clinical Research Associate (s), study sponsor and ancillary staff. **Required ... case report forms and other information related to data collection for clinical research . Must respond to queries in a timely fashion. Schedule on-site visits… more
- University of Southern California (Los Angeles, CA)
- …or Study Coordinator of issues or violations. + Acts as primary site contact with sponsor 's Clinical Research Associate (CRA) for externally sponsored ... Clinical Research Data Specialist IIApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical ... studies as a clinical trial assistant or clinical research associate is required....all study related correspondence with the investigative sites and sponsor including, but not limited to associated correspondence, CEC… more
- ThermoFisher Scientific (Las Vegas, NV)
- …the successful completion and filing of case report forms and source documents for clinical research studies. Works with sponsor representatives at all ... safety and positive impact on patient's lives. As a Research Team Clinical Data Associate ,...accurate and timely completion of study CRFs to meet sponsor requirements and deadlines. Informs Research Team… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate , you...research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent ... regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research 's applicable SOPs and working practices....is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely with… more
- ICON Clinical Research (Los Angeles, CA)
- …friendliest people in the sector, and you'll be helping shape an industry. As a Clinical Research Associate at ICON, you'll work within a large-scale, ... CRA II or Senior CRA (Single- Sponsor ) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an… more
- Rush University Medical Center (Chicago, IL)
- …**Shift 1** **Work Schedule:** 8 Hr (8:00:00 AM - 4:30:00 PM) **Summary:** The Associate Clinical Research Coordinator is a highly organized individual who ... disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
- Hartford HealthCare (West Hartford, CT)
- …turn to us. *Job Summary:* As a specialized research professional the Clinical Research Associate (CRA) collaborates with the Principal Investigator (PI) ... these duties, the CRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate * *… more
- ManpowerGroup (Stanford, CA)
- Our client is looking for Clinical Research Coordinator Associate located at Stanford, CA **Job title: Clinical Research Coordinator Associate ** ... Allergy** and **Critical Care Medicine is seeking a temporary/casual Clinical Research Coordinator Associate ** (CRCA)...* The CRCA interacts with a variety of study sponsor and regulatory agencies that include the NIH auditors,… more
- IQVIA (Carlsbad, CA)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- WuXi AppTec (Natick, MA)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... documentation of activities and findings as required by WuXi Clinical and sponsor . + Performs data quality...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I… more
- Cedars-Sinai (Los Angeles, CA)
- …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate I, you will work directly with a ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 4809 **Working Title** : Clinical Research Associate I -… more
- Cedars-Sinai (Los Angeles, CA)
- …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate II, you will work directly with a ... and ability to become proficient using related organizational and sponsor software programs. **Physical Demands:** **About Us** Cedars-Sinai is...the most. **Req ID** : 5409 **Working Title** : Clinical Research Associate II -… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Dec 08, 2023 Requisition # 101673 ... Stanford University's Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA)...**Duties Include*:** + Serve as the primary contact with research participants, sponsor , and regulatory agencies. +… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …**Description** JOB DESCRIPTION: ** This position is located in the Office of Research -Woodruff Industry Sponsored Clinical Trials department. ** + Provides ... **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate… more