Chief Risk Officer Jobs in Cambridge

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Search Results - Chief Risk Officer Jobs in Cambridge

Oncology Early Stage Clinical Scientist (Director, Non-MD)

Pfizer-Cambridge-today

as requested. MINIMUM QUALIFICATIONS / KEY SKILLS • Relevant PhD or PharmD and a minimum of 5 years of experience in a similar role in industry/CRO, OR • MS and a minimum of 7 years of experience in a similar role in industry/CRO, OR • BA/BS...

Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)

Pfizer-Cambridge-yesterday

development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. MINIMUM QUALIFICATIONS • PhD/Pharm D in a relevant Science discipline and minimum of 2 years Clinical Research experience in industry/CRO...

Oncology Late-Stage Clinical Scientist (Director, Non MD)

Pfizer-Cambridge-today

development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. MINIMUM QUALIFICATIONS • PhD/Pharm D in a relevant Science discipline and minimum of 5 years Clinical Research experience in industry/CRO...

Vice President Quality Assurance

Cambridge-pharmiweb.jobs-2 days ago

discipline; MBA preferred. • 15+ years of progressive QA leadership experience in pharmaceutical, biotechnology, or CRO environments. • Deep knowledge of GCP, ICH guidelines, and international regulatory inspection practices. • Proven success building...

Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)

Pfizer-Cambridge-today

US Business Development Director

VCLS-Cambridge-workable.com-today

by curiosity, purpose, and the desire to make an impact—for clients and ultimately for patients. • 8+ years of BD experience in Biotech, Medtech, CRO, or regulatory/scientific consulting. • Proven ability to close high-value, complex, science-driven...

Oncology Late Stage Clinical Scientist (Senior Manager, Non MD)

Pfizer-Cambridge-today

Senior Medical Coder

Cambridge-pharmiweb.jobs-3 days ago

healthcare background; advanced degree preferred. • 5-8+ years of medical coding experience in clinical research, ideally within CRO, pharmaceutical, or biotech environments. • Strong working knowledge of MedDRA and WHODrug dictionaries, including version...

Project Coordinator

ClinLab Solutions Group-Cambridge-yesterday

by developing dashboards, metrics, Gantt charts, and other project tracking tools. • Gather feedback from internal scientists, external vendors/CROs, and functional leads to ensure alignment on expectations and timelines. • Identify potential bottlenecks...

Associate Director, Group Lead, Data Management Reporting and Analytics

Pfizer-Cambridge-dejobs.org-6 days ago

or related field with 5 to 7 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency OR Masters or doctoral degree w Five or more years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency...

Senior Manager, Inspection Management

Moderna-Cambridge-today

authority inspections. • Experience with work in the Regulatory Intelligence area. • Experience developing responses to regulatory authority inspection findings. • Experience working with CROs, vendors, and relationship management. • Leadership skills...

Statistical Project Leader

Sanofi-Cambridge-mindmatch.ai-1 week ago

development, including experience with Biotech, pharma, Clinical Research Organizations (CROs), health authorities and academic clinical research centers • Broad knowledge and good understanding of advanced statistical concepts and techniques; being able...

Director, Toxicology

Editas Medicine-Cambridge-workable.com-1 month ago

sections of US and international regulatory applications • Manage CRO relationships and collaborate with the internal team to drive CRO selection, study monitoring and reporting to ensure scientific rigor, meeting timelines, budgets, and regulatory...

Development Scientific Director, Ophthalmology

Cambridge-pharmiweb.jobs-yesterday

And/Or Experience Required: • Ph.D. preferred, Masters degree considered for candidates with extensive experience. • A minimum of 3 years of phase I-III clinical trial/drug development experience within the ophthalmology/retina pharmaceutical industry or CRO...

Senior Manager, Portfolio Sourcing

Pfizer-Cambridge-dejobs.org-3 days ago

of Requests for Proposals and bid analyses. + Requests competitive bids/proposals from CRO Preferred Providers & other technical service providers + Pressure-tests and analyzes budget proposals and provides recommendations and analysis to internal...