Regulatory Affairs Cro Jobs

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Senior Clinical Trials Manager  

XYone Therapeutics Inc - Canton, MA, United States

with study sites and investigators, vendors, selection of vendors including CROs, monitoring trial progress, ensuring regulatory compliance, and managing study budgets and timelines. You will also collaborate

from: linkedin.com - Yesterday

Senior Director Regulatory Affairs  

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 - 5 days ago

Senior Scientist II, In Vivo Ocular Pharmacology  

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

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from: resume-library.com - 7 days ago

Toxicologist  

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 - 5 days ago

Sr. Scientific Program Manager  

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 - 9 days ago

Manager, Companion Diagnostic Operations  

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

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from: resume-library.com - 9 days ago

Regulatory Operations Contractor  

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 - 23 days ago

Senior Clinical Trial Manager  

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 - 26 days ago

Sr. Manager, Large Molecule Analytical Development  

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 - 13 days ago

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senior manager, cmc regulatory affairs  

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 - 24 days ago


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