Regulatory Assistant

24 Apr 2024
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Description: Will assist other regulatory coordinators with their duties. This position will focus primarily on pharmaceutical sponsor studies. This is a group of individuals who handle all of administrative work for the active and continuing studies regulatory work. They will work with PIs, clinical coordinators and the IRB to make sure regulatory documents are approved and correct for all of the pharmaceutical research studies in medical oncology. The regulatory coordinators and assistants do not work with patients or in the clinics at all.

Regulatory Assistant Essential Functions

Credentials, Certifications & Signature Records

File current records for MedOnc staff

Add or update study team in myIRB

New Study Reg Packet Requests

Additional Skills & Qualifications:

Must have an associates or bachelors degree and be interested in clinical research, no prior research experience is necessary.

About Actalent 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.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Full-time
  • ID: #51547698
  • State: Missouri St louis 63011 St louis USA
  • City: St louis
  • Salary: USD TBD TBD
  • Showed: 2024-04-24
  • Deadline: 2024-06-23
  • Category: Et cetera
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