What are the responsibilities and job description for the Study Director, In Vivo Oncology, Preclinical position at Crown Bioscience?

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 $100,000.00 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.

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Salary : $86,389 - $100,000

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Research Associate I - In Vivo

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JOB SUMMARY : The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within t...

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