Clinical Regulatory Affairs Jobs

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Clinical Scientist  

TalentCraft - Alameda, CA, United States

. - Conduct literature reviews and contribute to competitive assessments within each therapeutic area. - Collaborate on projects with other Clinical functions and across project teams (Regulatory, Medical

from: linkedin.com - 2 days ago

Manager, Clinical Supply Chain  

Kiniksa Pharmaceuticals - Lexington, MA, United States

protocols and design appropriate supply chain strategy Work collaboratively with Clinical Operations, Quality Assurance and Regulatory Affairs Interpretation of a protocol or study overview to calculate total

from: linkedin.com - 5 days ago

Clinical Trial Associate  

Beacon Hill - Waltham, MA, United States

in clinical drug development with knowledge of First in Human trials Experience with regulatory affairs, including IND/CTA submissions Experience working on dermatology

from: linkedin.com - 5 days ago

Medical Officer (Vaccine Research) - NIH  

Kelly - Rockville, MD, United States

the safety of the drug in question (5) Evaluate annual IND annual reports for medical safety and report findings to Regulatory Affairs Branch (RAB). (6) Provide medical expertise in protocol follow-up stages

from: linkedin.com - 5 days ago

Director Medical Writing  

Life Science People - Cambridge, MA, United States

, investigator brochures, clinical study reports, and regulatory submission documents (INDs, NDAs, MAAs). Collaborate with cross-functional teams, including clinical development, regulatory affairs, biostatistics

from: linkedin.com - 3 days ago

Director of Regulatory Affairs  

Simply Biotech - Aliso Viejo, CA, United States

responsible for the duties listed below. Immediate opening for a Director of Regulatory Affairs with a biopharmaceutical company in Aliso Viejo, CA who possesses: Understanding of clinical evaluations

from: linkedin.com - 2 days ago

Senior Quality Assurance Specialist  

BioPhase - , CA, United States

, Regulatory Affairs, Medical Affairs, and Pharmacovigilance. Support joint efforts in training on company procedures, GCP regulations, and documentation systems to assure compliance with company policies

from: linkedin.com - 2 days ago

Senior Director Quality Assurance  

Planet Pharma - Brisbane, CA, United States

quality performance, trends, and areas for improvement. Collaborate with cross-functional teams, including clinical operations, regulatory affairs, pharmacovigilance, and other relevant departments

from: linkedin.com - 2 days ago

Clinical Technical Writer  

Apex Systems - Burlingame, CA, United States

member of the regulatory affairs team working primarily with the company's wearable devices and digital health solutions. *SOFTWARE AS A MEDICAL DEVICE* Draft regulatory submission documents under guidance

from: linkedin.com - 2 days ago

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Senior Director GCP Quality Assurance  

Meet - South San Francisco, CA, United States

to clinical quality assurance. Establish and monitor quality metrics and key performance indicators. Collaborate with cross-functional teams, including clinical operations, regulatory affairs

from: linkedin.com - 3 days ago


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