Clinical Operations Administrative Support at PSI CRO
Mississauga, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

01 Nov, 25

Salary

0.0

Posted On

01 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Training

Industry

Hospital/Health Care

Description

Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description
In this role, you will provide project administrative support, manage documents, study-specific trackers, liaise with study vendors and members of the clinical project team.

QUALIFICATIONS

  • College or university degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
  • Proficiency in German and English
    Additional Information
    Take the next step in your career and join a company that genuinely focuses on its people.

ABOUT US

PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 2,700 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives.

Responsibilities
  • Exchanges project-specific information and documents with other PSI departments, sites and vendors
  • Maintains information in study-specific and corporate tracking systems
  • Supports regulatory and ethics committee submissions and notifications
  • Assists with organization of internal team meetings
  • Assists with preparation of draft agendas for, and minutes of, internal team meetings
  • Assists with preparation, conduct and follow-up of Investigator Meetings
  • Assists with clinical supplies order, receipt, inventory storage, distribution, return/recall and reconciliation at either PSI warehouse or as defined by the project team
  • Assists with preparation for and follow-up on TMF and systems audits and inspections
  • Maintains, performs regular periodic checks of, and files study related documents in the TMF on a site and country level
  • Assists with translations of study-specific documents
  • Assists with safety information flow with investigative sites
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