Regulatory Affairs Cro Jobs

Medpace, Inc. - Cincinnati, Ohio

Sciences, or other advanced degree. Minimum of 5 years of experience or equivalent of regulatory drug development. Expert knowledge of regulatory affairs within one or more therapeutic areas; Professional

from: resume-library.com - 12 days ago

Manpower San Diego - San Diego, CA, United States

Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical

from: linkedin.com - 17 days ago

SPECTRAFORCE - San Diego, CA, United States

, Regulatory Affairs, Pharmacovigilance & Legal departments, regulatory agencies, CROs, clinical investigators, etc. Ability to interpret and apply practical knowledge of regulations and guidelines

from: linkedin.com - 21 days ago

AnaptysBio Inc - San Diego , California 92121 , United States

, and regulatory affairs Proven ability to plan, conduct and manage clinical operations from early through late phase trials, with global trial experience is preferred. Demonstrated ability to manage CROs, central

from: jobtarget.com - 14 days ago

Beacon Hill Staffing Group - Park Ridge, IL, United States

, review protocols/reports, and ongoing data analysis. Coordinate with Regulatory Affairs/Quality Assurance/Supply Chain to ensure project deliverables adhere to company standards. Work with teams

from: linkedin.com - 21 days ago

CommonSpirit Health - Phoenix, Arizona

Organization (CRO) activities as well as the conduct of clinical trials at a site level. A unique skill-set with high attention to detail and subject matter expertise in Clinical Research Regulatory Affairs

from: resume-library.com - 23 days ago

Spark Therapeutics - Philadelphia, PA, US

to completion. Internal and External Contacts Internal Spark Contacts: Clinical Development Clinical Operation Regulatory Affairs Biometrics Corporate Quality Assurance Medical Affairs Cross-functional teams

from: Spark Therapeutics - 20 days ago

AstraZeneca - Mississauga, Canada

development, clinical operations, data management, statistics, and regulatory affairs. CIS will liaise with both the internal clinical teams and external CROs where applicable. CIS will work closely

from: jobrxiv.org - 18 days ago

Theradaptive - Remote, United States

and/or combination product clinical trials, quality assurance, and regulatory affairs within the biotech or pharmaceutical industry. * Strong leadership experience overseeing clinical operations teams, while managing

from: jobrxiv.org - 28 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 - 5 days ago