Clinical Study Administrator — Long-Term Role with Full Benefits

Kelly Services

Irvine (CA)

On-site

USD 60,000 - 85,000

Full time

14 days+

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Benefits offered by this job

Medical
Dental
Vision
401K
Paid time off
Holiday pay
Sick/personal time

Job summary

Kelly Science and Clinical FSP is seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc.

This role is full-time and is offering full benefit options. Kelly Science and Clinical is seeking a candidate to support the clinical study staff within Clinical Operations, perform routine and technical duties,

Qualifications

  • Bachelor’s Degree required.
  • Prior clinical research experience preferred.
  • Minimum 1 year of admin support experience.
  • Clinical/medical background beneficial.
  • Proficient with Microsoft Office suite.

Responsibilities

  • Support clinical study staff and project managers.
  • Track study data and assist with essential documents.
  • Prepare study mailings and meeting materials.
  • Assist payments/tracking for patient reimbursements.
  • Enter data in systems and run reports.
  • Coordinate IRB/IEC renewal activities.
  • Organize investigator and expert panel meetings.
  • Ensure communication with managers and team members.
  • Participate in process improvement activities.

Skills

Clinical research experience
Administrative support experience
Clinical/medical background

Education

Bachelor’s Degree

Tools

MS Office

Job description

Kelly Science and Clinical FSP is seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc.

This role is full-time and is offering full benefit options. Kelly Science and Clinical is seeking a candidate to support the clinical study staff within Clinical Operations, perform routine and technical duties,

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