Regulatory Affairs Cro Jobs
Brio Group - , NC, United States
Job Title : Regulatory Affairs Officer Company : Biopharma Organization Location : Hybrid, RTP Area Brio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent
from: linkedin.com - 10 days ago
Abbott Laboratories - Santa Clara, California
agency meetings. Works collaboratively with R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk
Register your RESUMEfrom: resume-library.com - 5 days ago
Rivus Pharmaceuticals - Charlottesville, VA, United States
and internal contractors , external CROs, and other vendors, as necessary.. Establish relevant processes and procedures to support the Regulatory Affairs function Provide mentorship and guidance to direct
from: linkedin.com - 11 days ago
PepGen - Boston, MA, United States
safety. Responsibilities Lead the cross functional study team for the EDODM1 Phase 1 study, including clinical monitors, data management, biostatistics, medical writing, safety, regulatory affairs
from: linkedin.com - 12 days ago
Mindlance - Auburn, Washington
Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical
Register your RESUMEfrom: resume-library.com - 8 days ago
i-Pharm Consulting - Boston, MA, United States
with cross-functional teams, including Clinical Development, Regulatory Affairs, Quality Assurance, and other departments, to ensure seamless integration and coordination of clinical activities. Establish
from: linkedin.com - 13 days ago
BioPhase - , CA, United States
Monitor, Regulatory Affairs, CRO, vendors and Investigators/site staff). Education/Experience Requirements: Bachelor’s in Life Sciences or equivalent. Graduate degree preferred. Therapeutic experience
from: linkedin.com - 18 days ago
Medpace, Inc. - Cincinnati, Ohio
Management, and Biostatistics. Qualifications : • PhD in Life Sciences or PharmD • 3+ years of regulatory affairs experience in a CRO or Pharmaceutical industry Medpace Overview : Medpace is a full-service
Register your RESUMEfrom: resume-library.com - 12 days ago
Beacon Hill - Boston, MA, United States
Recent Pharma/ CRO experience required Regulatory Operations Contractor Regulatory Affairs Location(Boston) Contract Term: Contract through EOY with possible extension Should have strong Word, PDF
from: linkedin.com - 15 days ago
Manpower San Diego - San Diego, CA, United States
Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical
from: linkedin.com - 17 days ago
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