Regulatory Affairs Cro Jobs

89bio - , CA, United States

, Clinical Development, CMC, Medical Affairs, Regulatory Affairs, CROs, CDMOs, Clinical Trial Sites, and laboratories. This role may have future leadership responsibilities building out a team and require

from: linkedin.com - 2 days ago

SciPro - , NJ, United States

the company's regulatory strategy having leadership over all regulatory activities Oversee product registration and submission Ensure compliance with FDA Work closely with CROs and manage relationships Provide

from: linkedin.com - Yesterday

Katalyst Healthcares & Life Sciences - South San Francisco, California

Programming, Clinical Operations, Clinical Research, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors. Establish

from: resume-library.com - 2 days ago

i-Pharm Consulting - , MA, United States

permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs

from: linkedin.com - Yesterday

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 - 4 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

from: resume-library.com - 2 days ago

Rivus Pharmaceuticals - Charlottesville, VA, United States (+1 location)

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 - 5 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 - 6 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

from: resume-library.com - 6 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 - 7 days ago