Manage the conduct of study activities in compliance with the protocol, amendments, and facility SOPs * May also assist in the further development of SOPs, training materials, and policies.
Quick apply
Manage the conduct of study activities in compliance with the protocol, amendments, and facility SOPs * May also assist in the further development of SOPs, training materials, and policies.
Quick apply
Manage the conduct of study activities in compliance with the protocol, amendments, and facility SOPs * May also assist in the further development of SOPs, training materials, and policies.
Serás responsable de diseñar experiencias, guiar journeys y coordinar a equipos de Data Analytics, CRO, CRM y SEO para convertir insights en decisiones medibles; también desarrollar talento y ...
New
Serás responsable de diseñar experiencias, guiar journeys y coordinar a equipos de Data Analytics, CRO, CRM y SEO para convertir insights en decisiones medibles; también desarrollar talento y ...
New
California, MO · On-site
$100 - $140/hr
Build and enforce pipeline management, forecasting, and Deal Desk governance * Establish pricing strategy and margin control mechanisms * Lead BD, KAM, Solution Architect, Sales Ops and Marketing ...
California, MO · On-site
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Manager, Commercial Operations Position Summary Catalent is seeking a Manager, Commercial ... Experience within a CDMO, CRO, biologics, cell & gene therapy, vaccine, or broader ...
Manager, Commercial Operations Position Summary Catalent is seeking a Manager, Commercial ... Experience within a CDMO, CRO, biologics, cell & gene therapy, vaccine, or broader ...
Manager, Commercial Operations Position Summary Catalent is seeking a Manager, Commercial ... Experience within a CDMO, CRO, biologics, cell & gene therapy, vaccine, or broader ...
Manager, Commercial Operations Position Summary Catalent is seeking a Manager, Commercial ... Experience within a CDMO, CRO, biologics, cell & gene therapy, vaccine, or broader ...
Manager, Commercial Operations Catalent is seeking a Manager, Commercial Operations to support our ... Experience within a CDMO, CRO, biologics, cell & gene therapy, vaccine, or broader ...
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Kansas City, MO · On-site
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Colaborarás estrechamente con equipos de Data Analytics, Digital Insights, CRO, CRM, SEO y PM para convertir hallazgos de research en decisiones accionables y medibles. * Gestión y desarrollo de ...
New
Kansas City, MO · On-site
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Colaborarás estrechamente con equipos de Data Analytics, Digital Insights, CRO, CRM, SEO y PM para convertir hallazgos de research en decisiones accionables y medibles. * Gestión y desarrollo de ...
New
In addition, the Senior RSM holds other assignments, such as Lead Regional Site Manager, Global Monitoring Operations Subject Matter Expert (SME), Contract Research Organization (CRO) Oversight ...
In addition, the Senior RSM holds other assignments, such as Lead Regional Site Manager, Global Monitoring Operations Subject Matter Expert (SME), Contract Research Organization (CRO) Oversight ...
California, MO · On-site
$205 - $215/hr
Lead CRO selection and management, oversee investigator recruitment and selection, study start‑up, enrollment, data collection, and drug projections. * Develop project timelines to meet ...
California, MO · On-site
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Lead CRO selection and management, oversee investigator recruitment and selection, study start‑up, enrollment, data collection, and drug projections. * Develop project timelines to meet ...
Kansas City, MO · On-site
$107K/yr
Colaborarás estrechamente con equipos de Data Analytics, Digital Insights, CRO, CRM, SEO y PM para convertir hallazgos de research en decisiones accionables y medibles. * Gestión y desarrollo de ...
New
Kansas City, MO · On-site
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Colaborarás estrechamente con equipos de Data Analytics, Digital Insights, CRO, CRM, SEO y PM para convertir hallazgos de research en decisiones accionables y medibles. * Gestión y desarrollo de ...
New
Experience with supervisory and financial management responsibilities in a regulatory affairs department of a CRO, pharmaceutical/biotech, or consulting firm. * Experience working in ...
Experience with supervisory and financial management responsibilities in a regulatory affairs department of a CRO, pharmaceutical/biotech, or consulting firm. * Experience working in ...
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Lead CRO selection and management, oversee investigator recruitment and selection, study start-up, enrollment, data collection, and drug projections. * Develop project timelines to meet departmental ...
California, MO · On-site
$205K - $215K/yr
Lead CRO selection and management, oversee investigator recruitment and selection, study start-up, enrollment, data collection, and drug projections. * Develop project timelines to meet departmental ...
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$180 - $220/hr
Experience with supervisory and financial management responsibilities in a regulatory affairs department of a CRO, pharmaceutical/biotech, or consulting firm. * Experience working in ...
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Experience with supervisory and financial management responsibilities in a regulatory affairs department of a CRO, pharmaceutical/biotech, or consulting firm. * Experience working in ...
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Monitor GA4 website analytics and drive conversion rate optimization (CRO) across websites, landing pages, and paid campaigns. * Manage and optimize Google Business Profiles listings across the ...
Saint Louis, MO · On-site
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Monitor GA4 website analytics and drive conversion rate optimization (CRO) across websites, landing pages, and paid campaigns. * Manage and optimize Google Business Profiles listings across the ...
Saint Louis, MO · On-site
Monitor GA4 website analytics and drive conversion rate optimization (CRO) across websites, landing pages, and paid campaigns. * Manage and optimize Google Business Profiles listings across the ...
Quick apply
Saint Louis, MO · On-site
Monitor GA4 website analytics and drive conversion rate optimization (CRO) across websites, landing pages, and paid campaigns. * Manage and optimize Google Business Profiles listings across the ...
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Louis, MO and founded in 1992, is a specialty manufacturer of early discovery research products (grade antibodies, proteins, sheath fluid, buffers) and a premier CRO/CDMO for grade custom antibodies ...
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$25.3K - $33.5K
2% of jobs
$33.5K - $41.8K
6% of jobs
$41.8K - $50.1K
4% of jobs
$50.1K - $58.3K
6% of jobs
$60.2K is the 25th percentile. Wages below this are outliers.
$58.3K - $66.6K
26% of jobs
The median wage is $70.4K / yr.
$66.6K - $74.9K
12% of jobs
$74.9K - $83.2K
15% of jobs
$86.1K is the 75th percentile. Wages above this are outliers.
$83.2K - $91.4K
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$91.4K - $99.7K
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3% of jobs
$25.3K
$75.1K
$116.3K
Full-time
Re-posted 14 hours ago
Senior Study Director/ Toxicologist
We are a growing mid-size organization with multiple sites looking for an accomplished Senior Study Director for our Toxicology division to assist with the growth we are experiencing and have plans to continue.
Say Goodbye to the bureaucracy and the administrative aspects of large cumbersome organizations and say Hello to the Science!
As a Senior Study Director, you will be responsible for participating in the design of non-clinical / preclinical studies as well as providing the scientific oversight of the study.
These studies will involve standard laboratory animal species (mice, rats, NHP, swine) across typical test article types (Vaccines, Biopharmaceuticals, Small Molecules).
This role will encompass multiple site studies and coordination thereof.
Maintaining and completing multiple projects simultaneously
Developing Protocols
Communicating with staff, management, and clients/sponsors
Analysis, interpretation, and reporting of data from non-clinical studies.
Manage the conduct of study activities in compliance with the protocol, amendments, and facility SOPs
May also assist in the further development of SOPs, training materials, and policies.
Proactive recognition, documentation, and resolution of any issues affecting the conduct of non-clinical studies.
Maintain knowledge of FDA and other regulatory guidelines
Work with the appropriate individuals to design and approve the study protocols
Perform other duties directed by the Director of Toxicology to meet client needs.
Experience, Education, and Specialized Knowledge and Skills:
Education
At least 5 years of experience directing non-clinical in vivo studies at a CRO or Pharmaceutical Company with a BS
-or-
At least 2 years of relevant industry/ toxicology experience with an MS or Ph.D./DVM
DABT or board eligible preferred
Demonstrated expertise in a scientific discipline
Essential Skills include: leadership, good organizational skills, knowledge of an experience with GLP (Good Laboratory Practices), AAALAC and USDA guidelines, experience using computer applications.
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Recruiting and staffing services
11 - 50 Employees
Fort Mill, SC, US
2018