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Sorrento Therapeutics Inc. is a fast growing, clinical stage, antibody-centric, biopharmaceutical company.
Life Science Research Professional 1 Job Family: Research Note: Not all unique aspects of the job are covered by this job description JOB PURPOSE:...
The Director, Global Talent Acquisition is responsible for the full cycle of talent acquisition
The Senior Manager, Medical Writing will be responsible for writing and coordinating the writing of peer-reviewed scientific publications
The Senior Manager of Data Management is accountable for the overall success of Data Management for his/her program
This position is accountable for defining the vision, mission and strategy for the function, which resides in the Clinical Operations organization
The Associate Director, Site Budgets & Contracts Management (SBCM) will lead the clinical SBCM function in the Clinical Operations Department
The Associate Director, Medical Writing will be responsible for writing and overseeing the writing of various clinical and regulatory documents
The Senior Clinical Science Dietitian (Sr. CSD) will work within the Clinical Science group
The Senior Manager, Regulatory Affairs will be responsible for managing regulatory activities
Position establishes, manages and performs multi-level inventory strategies to support customer and manufacturing sites
Ultragenyx is seeking a highly motivated individual for the role of Associate II, Regulatory Operations in the Regulatory Affairs Department
Have you always been motivated by your passion for cellular therapy and a desire to foster lasting relationships with science partners?
The US Medical Organization, Medical Director, Oncology, US Medical Leader (USML) for Acute Leukemia is the single point of accountability and matrix
Key Responsibilities Includes : Responsible for the direct management of Ambassadors; Responsible for ensuring the strategic focus, alignment,...
This QA/RA personnel will manage, coordinate and evaluate the company quality system and regulatory affairs.
In this research position you will participate in the discovery of compounds for the treatment of human diseases.
Summary As a key member of the CQA Audit and Inspection team, this position is responsible for leadership, planning, conduct, and reporting of GCP au
The candidate will have responsibility for directing the scientific aspects of preclinical oncology drug development programs and translational medic
The Regional Medical Liaison (RML) is a member of a field-based team of scientists who function as an extension of the Medical Affairs organization.