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
Register your RESUMEfrom: 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
Register your RESUMEfrom: 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
Register your RESUMEfrom: resume-library.com - 5 days ago
Beacon Hill Staffing Group - , 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
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