- RDI (Van Nuys, CA)
- RDI is seeking a detail-oriented and motivated Clinical Research Associate (CRA) to join our dynamic team. As a leading organization in clinical ... and our research teams, ensuring that all clinical trials are conducted according to regulatory ...preferred. At least 2 years of experience as a Clinical Research Associate or similar… more
- Axogen (Tampa, FL)
- …research activities, objectively target advancements in standards of care. Job Summary of the Clinical Research Associate II The Clinical Research ... support the CRM on project-level tasks. Requirements of the Clinical Research Associate II Bachelor's...back-up resource for other clinical studies in Clinical Ensures compliance with protocol and all regulatory… more
- IQVIA, Inc. (Parsippany, NJ)
- …in lieu of degree. *In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice ... visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP)...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Medix (Palo Alto, CA)
- …a position at one of our clients. Job Summary This is a fixed-term Clinical Research Associate /Data Manager position in the Pediatrics Hematology Oncology ... a primary contact. Documentation and Recording (20%): Maintain essential regulatory documents (CVs, medical licenses, CITI training) in the...in a medical field. Certification from the Society of Clinical Research Associates or Association of … more
- Allen Spolden (Alameda, CA)
- Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position ... regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits,… more
- IQVIA, Inc. (Durham, NC)
- …in lieu of degree. Req *Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. *i.e., Good Clinical Practice ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- Abbott (Alameda, CA)
- …Qualifications: BS degree in life sciences or equivalent with minimum 7 years of clinical research experience Must have 4 to 5+ years of relevant experience ... and to be flexible when priorities change. Working knowledge of GCP, Clinical and Regulatory Affairs. Proficient with Microsoft Suite. Travel Requirements… more
- New York Medical College (Hawthorne, NY)
- …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment,... clinical team. Ensure compliance with the Good Clinical Practice guidelines in clinical research… more
- IQVIA, Inc. (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 ... join our team . #C1920 #CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- Kura Oncology (Boston, MA)
- …comprised of regulatory affairs, clinical development, clinical operations, biostatistics, pharmacology, translational research , manufacturing, etc. to ... incorporation of multiple points of view. Solid understanding of drug development, clinical research , data analysis, Common Technical Document (CTD), ICH… more
