- 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 ... 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)
- …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 (Durham, NC)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will ... **Why Join Us?** Be part of a team that's driving innovation in clinical research . Your contributions will help shape the future of healthcare. Apply now and… more
- IQVIA (Overland Park, KS)
- …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
- 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
- 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
- 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
- Avania (OR)
- …Avania are hiring for the key dual role of Field Clinical Specialist (FCS) and Clinical Research Associate (CRA). This is a rare and highly sort after ... products, and the improvement/modifications of existing system(s). As a Clinical Research Associate (CRA) you...+ Act as main point of contact for the sponsor + Train study sites on performing Clinical… more
- ICON Clinical Research (Portland, OR)
- …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
- Hartford HealthCare (Bridgeport, CT)
- …to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator ... these duties, the SrCRA 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 This is… more
- Cedars-Sinai (Los Angeles, CA)
- …dedication pulses through Cedars-Sinai. **Dr. Lisa Bateman, MD is seeking a highly motivated Clinical Research Associate II to join her dynamic team!** Dr. ... provide top-tier care for those dealing with epilepsy. 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
- Cedars-Sinai (Beverly Hills, CA)
- …prediction of treatment outcomes. To learn more, please visit: Hitchins Lab | Cedars-Sinai. The Clinical Research Associate I works under the direction of a ... for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 5221 **Working Title** : Clinical Research Associate I -… more
- Weill Cornell Medical College (New York, NY)
- Title: Associate Director, Clinical Research Contracts Location: Midtown Org Unit: Contracts Work Days: Weekly Hours: 35.00 Exemption Status: Exempt Salary ... Office (JCTO), with a dotted line report to the Associate Director of Clinical Research ,...adherence to institutional guidelines and policies, as well as, sponsor requirements. Negotiates directly with external collaborators, as necessary.… 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
- Allucent (Cary, NC)
- …life-changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Research Associate (sCRA I) to join our A-team (remote, with ... and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate (1 Year Fixed Term) **School of Medicine, Stanford, California, United States** Research Post Date Sep 20, 2024 ... . The INSPIRE clinic is seeking to hire a Clinical Research Coordinator Associate (CRCA)...responsible for ensuring compliance with federal, state, local, and sponsor regulations and work independently under the direction of… more
- Providence (Portland, OR)
- **Description** The Clinical Research Coordinator I will function under the supervision of the Clinical Trials Manager. Coordinates and maintains diverse ... activities in the conduct of clinical research trials related to heart and...Bachelor's Degree with courses related to healthcare, science or research or equivalent educ/experience + Associate 's Degree… more