Regulatory Affairs Cro Jobs
MBX Biosciences, Inc. - Carmel, IN, United States
. Interface with MBX Regulatory Affairs on documents for FDA and other regulatory bodies. Monitor toxicology, TK, and pharmacology studies at CROs and Universities (GLP and nonGLP). Work with Medical/Clinical
from: linkedin.com - 4 days ago
CAMRIS - Bethesda, MD, United States
with vaccines and other biologics. American Board of Toxicology (DABT) required. Regulatory Affairs Certificate preferred. Experience specifically supporting drug discovery research and development
from: linkedin.com - 8 days ago
EyePoint Pharmaceuticals, Inc. - Watertown, Massachusetts
affairs to author nonclinical sections of global regulatory submissions. ID, select and manage nonclinical CROs, including forecasting and management of study financials. Serve as nonclinical lead
Register your RESUMEfrom: resume-library.com - 6 days ago
BioPhase - , CA, United States
Monitor, Regulatory Affairs, CRO, vendors and Investigators/site staff). Education/Experience Requirements: Bachelor’s in Life Sciences or equivalent. Graduate degree preferred. Therapeutic experience
from: linkedin.com - 25 days ago
Beacon Hill Staffing Group - Boston, MA, United States
Recent Pharma/ CRO experience required Regulatory Operations Contractor Regulatory Affairs Location(Boston) Contract Term: Contract through EOY with possible extension Should have strong Word, PDF
from: linkedin.com - 22 days ago
AbbVie - South San Francisco, California
development · Coordinate CDx operational activities with multiple functional areas (Biomarker Research, Regulatory, Pathology, Clinical Science, Biosample Management, Clinical Operations, and Medical Affairs
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 - 29 days ago
GSK - Waltham, MA (+1 location)
, and methodologies to enable effective collaboration with CRO/CDMO business partners to ensure efficiency and high quality of results. Partner with Quality Assurance and Regulatory Affairs-CMC to ensure completion
from: Pharmadiversityjobboard.com - 12 days ago
Randstad - northbrook, illinois (remote)
or academic with at least 3 years' experience directly in Regulatory Affairs or in CMC regulatory or role with CMC regulatory submission responsibilities in CMC related laboratories. Experience with global $80 - $92.69 per hour
from: randstadusa.com - 23 days ago
Daiichi Sankyo, Inc. - Atlanta, GA
; Participates in creation of developmental and regulatory strategy in collaboration with Regulatory Affairs; Drafts clinical development plans, protocol profiles and sections of key submission documents; Point
from: careerbuilder.com - 8 days ago
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