Clinical Regulatory Affairs Jobs

Coda Search│Staffing - New Haven, CT, United States

Specialists 2 and Regulatory Affairs Specialists 1 responsible for the management of study portfolios and the execution of regulatory activities for all types of clinical research studies across the lifecycle

from: linkedin.com - 10 days ago

Meet - , NJ, United States

and executing the clinical research strategy across preclinical development, clinical research, manufacturing, and regulatory affairs. Generates, executes, and preserves the project CDP and other clinical

from: linkedin.com - 8 days ago

Monteris Medical - Minnetonka, MN, United States

Event reporting for studies and ensures all applicable information is received by Regulatory Affairs and the clinical study sites. 6. Completes research tracking databases and spreadsheets to provide

from: linkedin.com - 8 days ago

Meet - Philadelphia, PA, United States

, writing clinical trial protocol, etc. Works collaboratively on a cross functional team working closely with Regulatory Affairs, Medical Affairs and Clinical Operations to ensure the study is conducted

from: linkedin.com - 8 days ago

Advanced Recruiting Partners - Raleigh, NC, United States

operations, medical affairs, regulatory affairs, and biostatistics Maintain current knowledge of industry regulations and guidelines relevant to clinical development Requirements: Master's degree or PhD

from: linkedin.com - 12 days ago

Meet - San Diego, CA, United States

operational excellence and ensure compliance with regulatory guidelines. Collaborate with cross-functional teams, including Clinical Development, Regulatory Affairs, Quality Assurance, and Data Management

from: linkedin.com - 3 days ago

Astrix - South Brunswick, NJ, United States

and documentation from Research and Development (R&D), Quality, Technical Operations, Labeling and other appropriate departments and internal stakeholders Represents Regulatory Affairs and provides regulatory advice

from: linkedin.com - 2 days ago

SoluStaff - Conshohocken, PA, United States

management accordingly. Actively collaborates with Global Regulatory Affairs team and cross functional colleagues in commercial operations, clinical development, quality, legal, compliance, etc. Monitor

from: linkedin.com (+3 sources) - 3 days ago

Hays - Bethesda, MD, United States

experimental protocols. • Strong working knowledge of Microsoft office; experience with SharePoint a plus. • Professional or educational background in a scientific field, clinical trials, regulatory affairs

from: linkedin.com - 4 days ago

EPM Scientific - , DE, United States

. Collaborate with cross-functional teams, including clinical development, regulatory affairs, and biostatistics, to gather necessary information and align on document content and timelines. Manage multiple

from: linkedin.com - 4 days ago