Chief Risk Officer Jobs in Boston
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Search Results - Chief Risk Officer Jobs in Boston
Paratus Sciences CorporationBostontrinethire.com
accountability.
You will be the operational backbone of our most critical near-term milestones across two pipeline programs. You will define how we work with CROs, how we govern our vendors, how we manage risk, and how we build the team that carries us through...
YO AI LabsBostoncareers-page.com
claims.
• Prepare structured, guideline-based written feedback.
Required Qualifications
• 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.
• Experience with clinical submissions, regulatory documentation...
CedentBostonappcast.io
and implementation of Standard Operating Procedures (SOPs) and workflows, ensuring regulatory compliance and adherence to industry best practices.
Oversee CRO activities, ensuring high‑quality deliverables, adherence to timelines, and efficient use of resources...
YO AI LabsBostoncareers-page.com
and analytical skills
Qualifications
• 5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research).
• MSc or PhD in Biostatistics, Statistics, or a related field.
• Experience with regulatory submissions and statistical...
AstraZenecaBostonappcast.io
safety and risk management experience in the pharmaceutical, biotech, CRO industry, academia or Health Authorities.
• Proven track record of successful clinical safety delivery with demonstrated examples of strategic influence to clinical studies/programs...
Frontier MedicinesBostonworkable.com
you will serve as a key operational contact for our CROs and trial sites, helping drive feasibility assessments, site selection, start-up, maintenance, and close-out.
This is a great opportunity for someone who wants hands-on ownership of trial...
Disability SolutionsBoston
making.
• Proven track record of working with investigators, site staff, external experts, CROs, and vendors.
Preferred Qualifications:
If you have the following characteristics, it would be a plus
• Advanced degree (e.g. MS, PhD, PharmD) in life...
YO AI LabsBostoncareers-page.com
Assessment
• Source Data Verification
• Clinical Protocol Interpretation
• TFL Analysis
• eCTD Knowledge
• Strong Written Communication & Collaboration
Qualifications
• 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting...
Bostonmedpace.com
quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work. Through our expedited PACE® Training Program, you will receive...
YO AI LabsBostoncareers-page.com
Source Data Verification
• Clinical Protocol Interpretation
• TFL Analysis
• eCTD Knowledge
• Strong Written Communication & Collaboration
Qualifications
• 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting...
ZifoBostonworkable.com
as well as collaborating with a global support team on larger projects.
As a consultant on our team, you will work with pharmaceutical, biotech, CRO, and regulated laboratory environments to design, configure, and deploy informatics solutions that improve...
YO AI LabsBostoncareers-page.com
Expectedness Determination
• Data Reconciliation
• Regulatory Documentation
• Structured Written Communication
• Attention to Detail
Preferred Qualifications
• 5+ years of pharmacovigilance or drug safety experience within a sponsor, CRO, or consulting...
Bostonicims.com
Safety, Regulatory, external CROs, and technology vendors to ensure high-quality, inspection-ready clinical data.
This is a hands-on role well suited for someone who thrives in a small biotech environment, can manage external partners effectively...
Frontier MedicinesBostonworkable.com
of these roles will serve as the operational leader for a program, translating clinical and business strategy into high-quality, on-time study delivery across regions and partners.
Working in close partnership with cross-functional leaders and CROs, you...
Bostonicims.com
in Biostatistics, Statistics, Epidemiology, or a related quantitative field
• A minimum of 3 years of substantive relevant experience required
• An ideal candidate will have 3-10 years of experience in clinical trials, pharmaceutical, biotech, or CRO environments...
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