Chief Risk Officer Jobs in Illinois
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Search Results - Chief Risk Officer Jobs in Illinois
Third Rock Ventures-Mundelein-
relationship (SAR) efforts and guide molecule optimization
• Manage and oversee work conducted at external CRO partners, including peptide synthesis, analytics, and related studies
• Review and interpret experimental data to inform molecule design and program...
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Empowered Staffing-Hoffman Estates-
part in producing high-impact creative across web, video, advertising, and brand design for both internal initiatives and client campaigns.
Responsibilities
• Design web graphics, hero images, CRO wireframes, and UI elements for landing pages...
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GQR-Mundelein-
readiness across the portfolio - the sponsor voice for every CRO, and the person leadership trusts when an inspector asks for the file. This is a build, not a cleanup. You set the TMF Reference Model mapping, the KPIs, and the inspection playbook the company...
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Champaign-carlehealth.org-
with the Defense Counsel Guidelines. This is done under the supervision of the SVP/Chief Risk Officer.
Collaboratively works with the SVP/Chief Risk Officer, the Associate Counsel: Litigation and Insurance, Executive Director of Risk Management and Clinical Risk...
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GQR-Mundelein-
and opportunities for improvement.
• Oversee CRO and vendor TMF activities, ensuring delegated responsibilities are executed in compliance with contractual and regulatory requirements.
• Serve as the TMF subject matter expert during audits, health authority...
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Chicago-icims.com-
record of prospecting (grants, publications), developing, and closing technical product and large capital equipment sales (100K+) to BioPharma and CROs, - Excellent verbal, written, interpersonal, computer, and technical communication, organizational...
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2 similar jobs: Springfield, Rockford
Redeployment-Mundelein-
Manage CROs, vendors, and external research partners, including timelines, deliverables, quality oversight, and issue resolution
• Establish and improve SOPs, laboratory documentation, sample tracking, and operational processes
• Partner with scientific...
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Chicago-pharmiweb.jobs-
in the pharmaceutical or CRO industry
• Experience monitoring Oncology clinical trials required, preferably heme/onc
• Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
• A clear communicator, problem-solver...
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Meet Life Sciences-Mundelein-
PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required
• 8+ years of medical writing experience within biotech, pharma, or CRO environments
• Demonstrated experience supporting complex clinical development programs...
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4 similar jobs: Sunnyvale, Sonoma, San Jose, Santa Rosa
Genesis Orthopedics & Sports Medicine-Oak Brook-workable.com-
Utilize IRT systems for patient randomization and drug accountability
• Maintain regulatory binders and essential study documents
• Assist with IRB submissions, regulatory maintenance, and study updates
• Communicate with sponsors, CROs, monitors...
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Deerfield (IL)-tiptopjob.com-
Serves as the primary operational lead for assigned studies, with accountability for timelines, budgets, resource planning, and delivery of key milestones. Leads cross:functional Study Teams, including CRO/vendor staff, ensuring alignment of clinical...
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ProTouch Staffing-Chicago-
supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies...
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ProTouch Staffing-Chicago-
supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies...
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ProTouch Staffing-Chicago-
supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies...
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ProTouch Staffing-Chicago-
Physician supporting Phase I-IV clinical trials in Chicago, IL. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies...
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