Study Director, In Vivo Oncology, Preclinical
Apply NowCompany: Crown Bioscience
Location: San Diego, CA 92154
Description:
JOB SUMMARY:
The Study Director/Scientist I is responsible for managing all phases of animal studies ensuring company strategies are implemented and company goals are achieved.
PRIMARY RESPONSIBILITIES:
Provide expertise in areas of design, implementation and analysis of in vivo, in vitro, or toxicology studies
Responsible for reviewing pre-clinical data
Provide hands-on technical execution of studies if required
Provide study design and effective protocol development
Develop, approve, and distribute study-related documents and other study tools
Oversee study planning, initiation, and study-closure processes
Create metrics, complete data analysis, study reports and presentations
Act as key point of contact and facilitate communication across Crown Bioscience departments, providing relevant information
Act as key point of contact for Crown Bioscience customers by providing regular updates
Review adverse events for safety and effectiveness information
Track and report progress of studies
Provide quality checks of study plans and reports, assisting QA with the development and implementation of corrective actions for addressing noncompliance issues
Maintain familiarity with current literature and trends
Prepare and present protocol and general study information to Clients and internal meetings
Conduct work activities in compliance with all relevant regulations including ethics, environmental health and safety, financial, human resources, SOPs, and general business policies, requirements and objectives
MINIMUM REQUIREMENTS:
Requires a PhD in Biomedical Science or a related discipline
Requires significant experience in oncology-related animal studies, preferably small molecules, biologics and immuno-oncology
Demonstrated experience leading teams and driving results
Strong understanding of oncology target biology and contemporary cell biology approaches to drug discovery
Willing and able to work under the pressure of deadlines and find solutions to meet timelines
Ability to work across teams by being a flexible team player with strong communication and interpersonal skills
Willing and able to work within a Quality System with oversight by QA and other regulatory bodies
Exceptional organizational and time-management skills
Ability to multi-task with a high degree of professionalism and diplomacy
PREFERRED REQUIREMENTS:
1-2 years of Post Doc translational biology/oncology experience in a research and/or industrial environment is preferred
Experience in a CRO setting and ability to multi-task, manage customer projects, and customer interactions is preferred
The salary range of the position in CA is $86,389.00 to $100,00.00 and is based off experience.
Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status.
The Study Director/Scientist I is responsible for managing all phases of animal studies ensuring company strategies are implemented and company goals are achieved.
PRIMARY RESPONSIBILITIES:
Provide expertise in areas of design, implementation and analysis of in vivo, in vitro, or toxicology studies
Responsible for reviewing pre-clinical data
Provide hands-on technical execution of studies if required
Provide study design and effective protocol development
Develop, approve, and distribute study-related documents and other study tools
Oversee study planning, initiation, and study-closure processes
Create metrics, complete data analysis, study reports and presentations
Act as key point of contact and facilitate communication across Crown Bioscience departments, providing relevant information
Act as key point of contact for Crown Bioscience customers by providing regular updates
Review adverse events for safety and effectiveness information
Track and report progress of studies
Provide quality checks of study plans and reports, assisting QA with the development and implementation of corrective actions for addressing noncompliance issues
Maintain familiarity with current literature and trends
Prepare and present protocol and general study information to Clients and internal meetings
Conduct work activities in compliance with all relevant regulations including ethics, environmental health and safety, financial, human resources, SOPs, and general business policies, requirements and objectives
MINIMUM REQUIREMENTS:
Requires a PhD in Biomedical Science or a related discipline
Requires significant experience in oncology-related animal studies, preferably small molecules, biologics and immuno-oncology
Demonstrated experience leading teams and driving results
Strong understanding of oncology target biology and contemporary cell biology approaches to drug discovery
Willing and able to work under the pressure of deadlines and find solutions to meet timelines
Ability to work across teams by being a flexible team player with strong communication and interpersonal skills
Willing and able to work within a Quality System with oversight by QA and other regulatory bodies
Exceptional organizational and time-management skills
Ability to multi-task with a high degree of professionalism and diplomacy
PREFERRED REQUIREMENTS:
1-2 years of Post Doc translational biology/oncology experience in a research and/or industrial environment is preferred
Experience in a CRO setting and ability to multi-task, manage customer projects, and customer interactions is preferred
The salary range of the position in CA is $86,389.00 to $100,00.00 and is based off experience.
Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status.