Regulatory Affairs Cro Jobs

Stratacuity: Proven Scientific Placement - Boston, MA, United States

or medical discipline and possess at least 5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or related industry. Additional Skills, licenses, or certifications

from: linkedin.com - 4 days ago

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 - 8 days ago

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 - 8 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 - 7 days ago

GForce Life Sciences - Waltham, MA, United States

and investigator sites, interface with internal departments clinical operations, medical information, regulatory affairs, product development, quality assurance, biostatistics, data management, and legal

from: linkedin.com - 5 days ago

Abbott Laboratories - Santa Clara, California

accurate, succinct summaries of clinical results at industry gatherings, investigational meetings and regulatory agency meetings. Works collaboratively with R&D, Clinical R&D, Regulatory Affairs, Library

from: resume-library.com - 5 days ago

GForce Life Sciences - Princeton, NJ, United States

, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance Required Skills

from: linkedin.com - 6 days ago

GForce Life Sciences - Trenton, NJ, United States

, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance Required Skills

from: linkedin.com - 6 days ago

Abbott Laboratories - Maple Grove, Minnesota

and project timelines and ensure timelines are met. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical

from: resume-library.com - 5 days ago

Beacon Hill - , MA, United States

as the primary sponsor contact for clinical issues relating to assigned clinical trials. Providing clinical and medical support to the CRO, as well as regulatory, safety and other functions, for assigned clinical

from: linkedin.com - 5 days ago