Chief Risk Officer Jobs in Cambridge
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Search Results - Chief Risk Officer Jobs in Cambridge
LanceSoft Inc-Cambridge
Summary:
Pay Rate : $ 75.00 to$ 80.00 Per Hour
Summary / purpose of the position
Take responsibility for coordinating the clinical monitoring activities, overseeing the CRO clinical /site management activities and co-monitoring the assigned...
resume-library.com -
Stratacuity: Proven Scientific Placement-Cambridge
Location: Cambridge MA (Hybrid)
Therapeutic Area: Rare Disease
Job Overview: The Site Budgets and Contracts Contractor oversees clinical site contracting, coordinates with CROs, internal teams, and sites, ensuring agreements meet budget...
mindmatch.ai -
Bicycle Therapeutics-Cambridge
at the CRO and other clinical vendors; monitor status and provide real-time updates to program team; facilitate communication between bicycle and the Clinical CRO
Ensure all study activities are completed in accordance with country specific ICH GCP, health...
resume-library.com -
Manning Personnel Group, Inc.-Cambridge
but are not limited to:
• Analyze the accuracy of financial results, determine variance drivers and write performance commentary
• Manage monthly CRO and outside services accruals; Preclinical and Clinical spend
• Produce and distribute quarterly investor reporting...
mindmatch.ai -
The Fountain Group LLC-Cambridge
of action studies.
Responsible for data processing, interpretation, and presenting to cross functional team members.
Design and execute experiments to evaluate MoA, target dependency, off target liabilities, phenotypic responses.
Manage CRO’s to run cell...
resume-library.com -
GC Therapeutics-Cambridge
organizations (CROs) for animal studies. Manage relationships with collaborators and CROs.
• Establish IACUC protocols and ensure compliance with regulations.
Molecular Biology:
• Utilize techniques such as PCR, molecular cloning, and plasmid isolation...
mindmatch.ai -
The Fountain Group LLC-Cambridge
the monitoring and performing of notification and/or submissions for Individual Case Safety Reporting for Clinical Trial submission cross functionally (e.g. CRO, Partner, Clinical, and/or Regulatory) with DSPV Systems Team
Support DSPV Compliance with monitoring...
resume-library.com -
Cambridge
RWE analytics for pharma industry, CRO.
• Experience in burden of disease / HCRU / cost of illness, and/or pharmaco-epidemiological studies - please include publication in the resume....
pharmiweb.jobs -
Integrated Resources, Inc-Cambridge
responses.
Manage CRO s to run cell-based assays and other molecular biology techniques.
Experimental and intellectual contribution to cross-functional project teams.
Maintain up to date with relevant literature.
What minimum qualifications do we require...
resume-library.com -
Alnylam Pharmaceuticals-Cambridge
and selection of CROs and other 3rd parties
Qualifications
• Master’s Degree, PhD, PharmD, or M.D. with a strong clinical research background, or clinical trial/drug development experiences at various phases of development (Phase 1-3)
• Industry experience (6...
Randstad-Cambridge
The candidate will be expected to thrive in a fast-paced, dynamic, and nimble environment of an emerging company that depends on strong links and collaboration with external stakeholders (CRO partners, research organizations, alliance partners, etc.).
• Sound...
randstadusa.com -
Page Executive-Cambridge
desired.
• Drug discovery knowledge, biopharma CRO, and relevant business experience required.
• At least 5 years' experience selling to pharma and biotech preferred. Experience in in vivo pharmacology preferred.
• Masterful selling skills that result...
pageexecutive.com -
Cambridge
to cross-functional teams.
• Design and execute experiments to assess mechanisms of action, target dependencies, and phenotypic responses.
• Manage collaborations with CROs for cell-based assays and molecular biology techniques.
• Contribute...
pharmiweb.jobs -
Editas Medicine-Cambridge
detailed record electronically in accordance with Editas’ policy, analyze data and present at internal and external meetings.
• Manage interactions with vendors, CROs, KOLs, and academic collaborators.
Requirements
The Ideal Transcript:
To thrive...
workable.com -
Cambridge
or coordinate the development of study documents such as protocols and informed consent forms.
• Coordinate with internal teams, CROs, investigators, and regulatory agents for study planning and execution.
• Manage clinical records and documents in internal...
pharmiweb.jobs -
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