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Contribute to the design and execution of BD plans in close coordination with RSD leadership for identification, penetration and growth of RSD business and accounts located on the Midwest Region. This position can be located anywhere in the Midwest region.
The primary responsibilities of the Quality Specialist include ensuring GLP studies, GMP testing, and GMP manufacturing activities are executed in accordance with the appropriate regulatory bodies and internal procedures. In addition, the Quality Specialist is responsible for performing internal audits, ensuring timely completion of investigation documents, and providing training to peers on systemic requirements.
WuXi AppTec is seeking recent graduates that are passionate about data platform technology and the next generation digital data platform for our digital innovation future leadership training program.
These are unique opportunities for recent graduates to work across various areas of digital technology to help assess what interests them most and to get broad experience early in their career. Program trainees receive training while being mentored by senior technical experts and project managers. You will have the opportunity to shape your career as you develop your technical, consultative and project management skills.
The ideal candidate will have a combination of technical and soft skills, including the ability for data analytics and to think critically. Qualified candidates must be detail-oriented with excellent communication and writing skills.
Further, s/he must be organized with the ability to manage multiple deadlines simultaneously in a fast-paced environment.
- This is a full-time employment position offering comprehensive benefits, a competitive salary, paid training, and performance-based bonuses.
Job Summary: The Clinical Project Associate I provides administrative support to clinical research projects by assisting project teams in the completion of assigned project activities. This is an in-office position with that does not require travel.
Job Summary: The Associate Project Manager I assists the Project Manager and other senior management in clinical and/or data activities in a limited scope on the N. American portion of clinical research projects in order to assure applicable regulations, standard operating procedures and sponsor requirements are met. This position can be a combination of work from home and in office with limited travel.
Job Summary: The Associate Director, Clinical Operations provides leadership as a member of the senior management team overseeing the day to day activities of the project management team and clinical operations team; assists with the evaluation and implementation of systems and process to support efficient performance; and manages and coordinates clinical and/or data project services for sponsors to assure project/program milestones are met and applicable regulations are followed. This can be a work from home position and requires approximately 20% travel.
The Project Manager will manage and coordinate clinical and/or data project services for sponsors to assure project/program milestones are met according to contract and applicable regulations are followed. Preference for in-office over work from home with occasional travel depending on project.
Job Summary: The Senior Clinical Data Manager performs clinical database setup, maintenance, and data quality control functions through database lock in accordance with Good Clinical Practices (GCP), International Conference on Harmonisation (ICH), and ResearchPoint Global and Sponsor SOPs. This position can either be In-Office or WFH with less than 10% travel.
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An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
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