Seeking a detail-oriented Regulatory Assistant to assist our regulatory coordinators with administrative duties in pharmaceutical sponsor studies. This role primarily involves managing regulatory documents to ensure they are approved and correct for pharmaceutical research studies in medical oncology. You will collaborate with Principal Investigators (PIs), clinical coordinators, and the Institutional Review Board (IRB), but will not engage directly with patients or work in clinical settings.
This is a hybrid position requiring some days on-site in St. Louis, Missouri and some days remote.
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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