Regulatory Affairs Administrative Assistant

extra holidays
Work set-up: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

High School Diploma or equivalent required, Bachelor's Degree preferred., At least 1 year of Clinical Research experience is preferred., Minimum of 2 years of administrative experience in a fast-paced, regulated industry., Strong research, analytical, communication, and organizational skills, with proficiency in MS Office..

Key responsibilities:

  • Manage and oversee clinical trials regulatory activities and coordinate with Regulatory Affairs team.
  • Support review and filing of regulatory documents and IRB submissions.
  • Attend and contribute to team meetings, preparing agendas and minutes.
  • Assist in maintaining IRB study access and handle other assigned duties.

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DaVita Kidney Care Large https://careers.davita.com
10001 Employees
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Job description

Posting Date

07292025

825 S 8th StSte 400, Minneapolis, Minnesota, 554041208, United States of America

At DaVita Clinical Research, we find that our best leaders are those who create an inspiring vision, have a desire to shape the future of medicine, and empower their team to achieve success. They enjoy tackling difficult problems and believe that the best way to solve them is through a collaborative environment that involves team efforts. They take ownership of results and instill accountability in those they lead. They are driven, compassionate, strong communicators, relationship builders, and find real fulfillment in challenging and impactful work.

We are seeking a Regulatory Affairs Administrative Assistant to assist with the operational excellence initiatives for the DaVita Clinical Research team. This teammate will be responsible for all required regulatory documents necessary to support research studies for Clinical Trials to ensure all studies meet federal and GCP guidelines for research.

DCR prides itself on a culture of growth, transparency and feedback and would want our leaders to do that same. We want a teammate who is compassionate, purposeful and motivated by meaningful work.

ESSENTIAL DUTIES & RESPONSIBILITIES:

40% Manage and oversee clinical trials regulatory activities throughout the course of all studies. Provide oversight of DCR clinical trials Regulatory Affairs Coordinators for assigned projects and manage resources to ensure project needs are met.
Act as a main point of contact for information and escalation for issues related to site startup

15% Support the review of regulatory document filing once site startup packets are completed.

15% Attend team meetings, collaborate with the regulatory leadership to create regulatory meeting agendas and manage the meeting minutes.

20% Support the Regulatory Affairs Coordinators in reviewing IRB submissions for studies in startup

5% Update and maintain IRB study access for Alliance teammates 5% Other duties as assigned.

MINIMUM QUALIFICATIONS

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Analytical Skills
  • Computer Literacy
  • Organizational Skills
  • Teamwork
  • Communication
  • Problem Solving

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