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Scientist II, Pre-Clinical
4 months ago
Make an impact through innovation that is shaping the future of healthcare. At Biora, we are focused on creating better ways of developing and delivering life-improving therapeutics. We continually seek people with the motivation and skills to advance our mission.
Biora is a biotech company reimagining therapeutic delivery. By creating innovative smart pills designed for targeted drug delivery to the GI tract and systemic, needle-free delivery of biotherapeutics, we are developing therapies to improve patients' lives.
The Pre-Clinical Scientist II plays a key role in execution of pre-clinical experiments of Biora's drug delivery device products. The Pre-Clinical Scientist II participates in the design, execution, and interpretation of pre-clinical medium-large animal experiments and authors experimental study reports. The role is on-site and is located in San Diego, California.
RESPONSIBILITIES
* As a member of the research and development team, contributes scientific expertise to preclinical and translational studies, including participation in experimental design, execution, data analysis, interpretation, and reporting.
* Contributes to and reviews study designs and protocols, study reports, publications, and scientific literature reviews.
* Involvement in preclinical projects in development from scientific assessment of a pre-clinical project to final deliverable.
* Assists with field site questions during conduct of pre-clinical study as needed.
* Exercises independent judgment in the performance of technical responsibilities.
* Reviews results for completeness, accuracy, and consistency within defined test parameters.
* Recognizes when unresolved issues need to be escalated and takes immediate necessary follow-up action.
* Meets competency standards of the department.
* Ensures continuing education requirements are met.
This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as deemed necessary.
REQUIREMENTS
* Ph.D. degree in relevant biological science required with 2+ years within biopharma or drug delivery device Industry or CRO
* 2+ years of post-doctoral research experience within the industry preferred for Ph.D. candidates.
* 5+ years in Translational research and Pharmacology or other related areas within biopharma or drug delivery device Industry or CRO for Master or Bachelor candidates.
* Previous experience as a hands-on medium-large animal research scientist.
* Previous experience in Therapeutics Research or Development preferred.
* Proficiency in scientific writing.
* Ability to manage CRO or other BioA laboratory independently to achieve objectives.
* Ability to apply critical thinking skills to review and identify key strengths and weaknesses of study protocol(s).
* Must be able to handle a wide work variety and work in a fast-paced environment.
* Must be a team player who can work with experts from a broad range of disciplines including, but not limited to mechanical and software engineering, biochemistry and bioanalytical sciences, pharmacology, clinical science, quality, and project management.
* Must be detail-oriented, results oriented, organized, self-starter, and have an ability to prioritize workload.
* Scientific expertise or interest and ability to learn in the domain of assigned study/project is a plus.
* High level of autonomy and motivation.
* Quality focused and well organized.
* Strong communication skills (verbal and written).
* Ability to handle multiple tasks and to prioritize.
* Ability to synthesize information, good presentation skills.
* Excellent problem-solving capabilities.
* Capability to challenge decisions and status quo.
* Ability to work autonomously and to provide status reports efficiently and effectively.
* Ability to anticipate and timely escalate issues and to define appropriate action plans.
* Ability to draft and author scientific research publications and preclinical research reports.
* Willing and able to travel to local experimental study sites for study execution and supervision as needed (up to 25% of the time, with occasional interstate travel).
* Ability to work on-site.
* Must be legally authorized to be employed in the United States.
SALARY
* $110-135k base salary target based on education and experience.
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