- IQVIA (Tampa, FL)
- …candidates located East, Central or West Coast. **Job Overview** We are seeking a dedicated Clinical Research Associate ( CRA ) to join our team and ... IQVIA Early Clinical Development is hiring for CRA ...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
- General Dynamics Information Technology (Fort Detrick, MD)
- …**US Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a Clinical Research Monitor to support the Office of Regulated ... **HOW YOU WILL MAKE AN IMPACT:** **Develop a Clinical Monitoring Plan and monitor single site and multicenter clinical studies both inside and outside… more
- ConvaTec (Lexington, MA)
- …+ Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all operational aspects from start-up ... activities. + Support the selection, oversight, and management of Clinical Research Organizations (CROs) and other vendors...build solid professional relationships with key opinion leaders and clinical site staff to support clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Proficient ... applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical Development Lead) + Protocol and ICF...CRO scope of work, etc. + Review development of site and CRA training materials and presentation… more
- Otsuka America Pharmaceutical Inc. (GA)
- …Bachelor's degree in Life Sciences, Nursing, or related field. + 4+ years' experience in clinical research , site management, or field clinical support. + ... communication, data interpretation, and relationship-building skills. **Preferred Qualifications:** + Clinical Research Coordinator (CRC) certification or equivalent… more
- Loyola University Chicago (Chicago, IL)
- …to interact with internal and external constituents. Certificates/Credentials/Licenses + CCRA (Certified Clinical Research Associate ) or equivalent (SoCRA or ... Clinical Research Coordinator II (IITs) Thank...Research Participants, Sponsors, and Regulatory agencies. + Coordinate multi- site studies from startup through close-out. Facilitate and manage… more
- Bristol Myers Squibb (Seattle, WA)
- …+ Conduct literature review + Submit clinical documents to TMF + Develop site and CRA training materials and present these at SIVs and Investigator meetings ... + Review clinical narratives + Monitor clinical ...out the highest potential of each of our colleagues. **On- site Protocol** BMS has an occupancy structure that determines… more
- Edwards Lifesciences (Kansas City, KS)
- …in cardiology + Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical research experience ... within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with...a minimum of 5 years of work experience in clinical research monitoring, with a strong focus… more
- United Therapeutics (Research Triangle Park, NC)
- …Licensure and/or Compact State Licensure + Previous experience with all phases of clinical research + Demonstrated leadership experience as evidenced by the ... diligently, reducing their occurrence through proactive collaboration + Collaborate with Clinical Operations to monitor key performance indicators, enhancing… more
- Gilead Sciences, Inc. (Foster City, CA)
- …monitoring + Minimum of 2 years of experience as a Data Scientist, Clinical Research Associate , or Study Coordinator **Skills/Competencies** + Expertise ... + Bachelor's degree with 10 or more years of clinical research experience in the biotech or... experience in the biotech or pharmaceutical industry (eg, clinical development, site management, site … more