- SUNY Upstate Medical University (Syracuse, NY)
- …ship lab samples. Schedule and conduct follow up research appointments for clinical trial participants. Data collection and entry into paper and electronic ... Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO regulatory correspondence. Communication… more
- Childrens Hospital of The King's Daughters (Norfolk, VA)
- + GENERAL SUMMARY + The Clinical Research Associate is responsible for working directly with principal investigators to facilitate all aspects of research ... . Instrumental in study design, coordination, implementation, documentation and data management of research protocols to include budget preparation, monitoring… more
- ManpowerGroup (Lake Forest, IL)
- **Title:** Clinical Research Associate (CRA) **Location:** Lake forest, IL **Duration:** 12 Months **Remote role (occasional travel)** **Pay Range :** $25/hr ... $29/hr (On W2) We are looking for a " ** Clinical Research Associate (CRA)"** to...and regulatory requirements + Perform source document verification and data query resolution + Support start-up tasks such as… more
- IQVIA (Carlsbad, CA)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- SUNY Upstate Medical University (Syracuse, NY)
- …experience or equivalent combination of education and experience, experience with clinical research protocols, knowledge of medical terminology, computer skills, ... written/oral communication and organizational skills required. Preferred Qualifications: Previous clinical research experience with cardiology patients and SOCRA… 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
- SUNY Upstate Medical University (Syracuse, NY)
- …screen patients for clinical research trials; collect and submit clinical trial patient data . Perform various administrative duties, which may include ... proper collection and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications:… more
- IQVIA (Overland Park, KS)
- …customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.You should have: + A Bachelor's degree in ... our team** . \#C1920 \#CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- Cedars-Sinai (Los Angeles, CA)
- …which will empower tomorrow's medicine? **Dr. Piotr Slomka, Ph.D. is looking for a Research Associate Data Scientist to join a diverse team!** The ... **Job Description** **Grow your career at Cedars-Sinai!** Data is vital to advance clinical ...positron emission tomography (PET)/computed tomography (CT) angiography imaging. The Research Associate Data Scientist participates… more
- BeOne Medicines (Emeryville, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... Word, Excel, PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes… more
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