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We are seeking a detail-oriented and highly collaborative Scientist to act as a Study Director for in vivo toxicity and PK/TK studies. The successful candidate will direct these studies to ensure project timelines are met, and effectively communicate with project managers, clients, and internal teams.
Responsibilities :
Study direction of in vivo non-GLP and GLP general toxicology and PK/TK studies.
Initiate, monitor and oversee studies
Interpret experimental data
Author study protocols and reports.
Acts as a primary point of study contact
Maintain schedule of projects and timelines to meet client program milestones
Maintain the proper level of regulatory compliance for each study and addressing QA audit findings
Maintain and facilitate communication with sponsors and management
Help with training and/or mentoring of junior scientific staff.
Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties.
Work with support teams including sample management, vivarium, QC, RW, PM & QA, BD as well as PIs and management.
Other duties as assigned.
Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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We are seeking a detail-oriented and highly collaborative Scientist to act as a Study Director for in vivo toxicity and PK/TK studies. The successful candidate will direct these studies to ensure project timelines are met, and effectively communicate with project managers, clients, and internal teams.
Responsibilities :
Study direction of in vivo non-GLP and GLP general toxicology and PK/TK studies.
Initiate, monitor and oversee studies
Interpret experimental data
Author study protocols and reports.
Acts as a primary point of study contact
Maintain schedule of projects and timelines to meet client program milestones
Maintain the proper level of regulatory compliance for each study and addressing QA audit findings
Maintain and facilitate communication with sponsors and management
Help with training and/or mentoring of junior scientific staff.
Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties.
Work with support teams including sample management, vivarium, QC, RW, PM & QA, BD as well as PIs and management.
Other duties as assigned.
US-based CRO/CDMO providing drug discovery, testing, clinical, and manufacturing services to pharmaceutical and biotechnology companies.
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Mid · 2+ years experience
Onsite
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