- IQVIA (Overland Park, KS)
- …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 (Lincoln, NE)
- IQVIA is seeking Senior Clinical Research Associate IIs and Senior Clinical Research Associate IIIs based in the Mid-West, US and Northwest, US. ... degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate with...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
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago ... Clinical Practice (GCP) S/he will coordinate standard clinical research studies conducted by PI(s) which...and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Mar 01, 2024 Requisition # 102433 ... through global-reaching clinical research , we encourage you to apply! The Clinical Research Coordinator Associate (CRCA) will work with SCCR in… more
- Hartford HealthCare (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
- Hartford HealthCare (Hartford, CT)
- …And this is*your moment*. **Job:** **Administrative* **Organization:** **Hartford Hospital* **Title:** * Clinical Research Associate - Department Of ... stimulating work environment that inspires excellence. *Job Summary:* Job summary: Assists the Clinical Research Division of the Bone & Joint Institute by… more
- Cedars-Sinai (Los Angeles, CA)
- …dedication pulses through Cedars-Sinai. **Dr. Omar Al-Louzi, MD** **is seeking a highly motivated Clinical Research Associate II to join his dynamic team!** ... injury in neuro-immunological disorders and Multiple Sclerosis (MS). The Clinical Research Associate II will...trials. + Assists with preparing manuscripts, letters, and other research documents as needed. + Responds to sponsor… 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
- J&J Family of Companies (Columbus, OH)
- Clinical Research Associate II - 2406181956W **Description** Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Clinical Research ... impact health for humanity. Learn more at https://www.jnj.com/. Reporting to the Manager, Clinical Research Associates, the person in this role is responsible… more
- Merck (Columbus, OH)
- …as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops ... and expands the territory for clinical research , finding and developing new sites.... study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring… 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
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate (50% FTE/Fixed Term) **School of Medicine, Redwood City, California, United States** **New** Research Post Date 2 ... of Orthopaedic Surgery has an immediate opening for a Clinical Research Coordinator Associate (CRCA)...uphold Stanford University's compliance with federal, state, local, and sponsor regulation. + Drive to establish themselves as a… more
- Merck (OH)
- …and resolves site performance, quality, or compliance problems and escalates per defined Clinical Research Associate (CRA) Escalation Pathway as appropriate ... Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. + Develops… more
- IQVIA (Boise, ID)
- IQVIA is seeking a Clinical Research Associate 2's or Sr. Clinical Research Associate 2's with onsite monitoring experience. Must be based in the ... in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and… more
- Danaher Corporation (Chaska, MN)
- …vision is to relentlessly reimagine healthcare, one diagnosis at a time. The Sr. Clinical Research Associate (CRA) for Beckman Coulter Diagnostics is ... guides, study tools/worksheets) and ensure Trial Master File (TMF), Sponsor Site Files (SSF), and Investigator Site Files (ISF)...+ CLSI guidelines and Good Laboratory Practice (GLP) + Clinical research certification (ie, SOCRA, CCRA, CCRC)… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor /CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
- University of Southern California (San Diego, CA)
- Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate ... San Diego, California The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute… more
- System One (Philadelphia, PA)
- Senior Clinical Research Associate - Regional Location: Home Based, Philadelphia, PA Area Type: Full time Start Date: ASAP Are you an experienced Clinical ... all of the above! You are working for a sponsor , in a therapeutically aligned model supporting Endocrinology studies,...CRA (monitoring experience) + Industry experience: 5+ years of clinical research industry experience + Diabetes experience… more
- Actalent (St. Louis, MO)
- …- At least 3 years as a full-time Lead regional monitor working for a sponsor or Contract Research Organization (CRO) - Experience managing aspects of CRO ... Location: Mountain time The candidate will be primarily responsible for assisting the Clinical Operations team in the execution of clinical trial deliverables in… more