Senior Scientist II, Toxicology and Toxicology Program Management
Posted on Sep 21, 2024 by Deciphera Pharmaceuticals
Waltham, MA
Research
Immediate Start
Annual Salary
Full-Time
Job Description
What You’ll Do:
Ensures scientific and operational excellence across the toxicology and safety pharmacology activities.
Collaborates closely with Nonclinical R&D Team, consultants, and external CRO partners to ensure studies are fit for purpose, completed on time, on budget and meet quality standards.
Contribute to writing and editing nonclinical safety study research reports to support regulatory filing including pre-IND, IND, IND annual updates, IB, as well as relevant sections to support US and International regulatory filings.
Track and manage timelines for Nonclinical R&D studies across various stakeholders identifying interdependencies, milestones, and risks.
Align internal business needs and expectations with external CRO partners.
Manage, setup, and maintain purchase orders in company purchasing systems.
Ensure compliance with global non-clinical safety studies regulatory guidelines.
Ensure completion of non-clinical safety studies to support program timelines and goals.
What You’ll Do:
Ensures scientific and operational excellence across the toxicology and safety pharmacology activities.
Collaborates closely with Nonclinical R&D Team, consultants, and external CRO partners to ensure studies are fit for purpose, completed on time, on budget and meet quality standards.
Contribute to writing and editing nonclinical safety study research reports to support regulatory filing including pre-IND, IND, IND annual updates, IB, as well as relevant sections to support US and International regulatory filings.
Track and manage timelines for Nonclinical R&D studies across various stakeholders identifying interdependencies, milestones, and risks.
Align internal business needs and expectations with external CRO partners.
Manage, setup, and maintain purchase orders in company purchasing systems.
Ensure compliance with global non-clinical safety studies regulatory guidelines.
Ensure completion of non-clinical safety studies to support program timelines and goals.
Reference: 202107732
https://jobs.careeraddict.com/post/95493111
Senior Scientist II, Toxicology and Toxicology Program Management
Posted on Sep 21, 2024 by Deciphera Pharmaceuticals
Waltham, MA
Research
Immediate Start
Annual Salary
Full-Time
Job Description
What You’ll Do:
Ensures scientific and operational excellence across the toxicology and safety pharmacology activities.
Collaborates closely with Nonclinical R&D Team, consultants, and external CRO partners to ensure studies are fit for purpose, completed on time, on budget and meet quality standards.
Contribute to writing and editing nonclinical safety study research reports to support regulatory filing including pre-IND, IND, IND annual updates, IB, as well as relevant sections to support US and International regulatory filings.
Track and manage timelines for Nonclinical R&D studies across various stakeholders identifying interdependencies, milestones, and risks.
Align internal business needs and expectations with external CRO partners.
Manage, setup, and maintain purchase orders in company purchasing systems.
Ensure compliance with global non-clinical safety studies regulatory guidelines.
Ensure completion of non-clinical safety studies to support program timelines and goals.
What You’ll Do:
Ensures scientific and operational excellence across the toxicology and safety pharmacology activities.
Collaborates closely with Nonclinical R&D Team, consultants, and external CRO partners to ensure studies are fit for purpose, completed on time, on budget and meet quality standards.
Contribute to writing and editing nonclinical safety study research reports to support regulatory filing including pre-IND, IND, IND annual updates, IB, as well as relevant sections to support US and International regulatory filings.
Track and manage timelines for Nonclinical R&D studies across various stakeholders identifying interdependencies, milestones, and risks.
Align internal business needs and expectations with external CRO partners.
Manage, setup, and maintain purchase orders in company purchasing systems.
Ensure compliance with global non-clinical safety studies regulatory guidelines.
Ensure completion of non-clinical safety studies to support program timelines and goals.
Reference: 202107732
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