Clinical Trial Manager at ICON
Remote, Scotland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

03 Sep, 25

Salary

0.0

Posted On

04 Jun, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

WE ARE HIRING A CLINICAL TRIAL MANAGER TO START ASAP!

The role can be fully homebased in the UK and this is anon-travelling position.
This is a great opportunity to steer your career towards clinical trial management. It would suit a Junior CTM,or experienced Senior Clinical Project Specialist with solid multiple country exposure, looking for their first CTM position. Global clinical trial experience is essential to succeed!
You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world’s leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

Responsibilities
  • Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials
  • Vendor management and support vendor relationships
  • Work with the clinical trial management staff to support the execution and monitoring of clinical studies and trial deliverables
  • Contribute to and support with the preparation, writing and review of study related documents including but not limited to, clinical protocols, study guides, monitoring plans, e(CRF)s, subject information sheets and consent forms, clinical study report, regulatory submissions and publications
  • Coordinate the activities associated with site start-up and overall trial management
  • Coordinate study level investigational product arrangements, accountability and reconciliation
  • Contribute to, or coordinate preparation and conduct of site initiations, monitors’ workshops (as applicable) and investigator meetings (as applicable)
  • Assists in preparing and managing Study Budgets and timelines
  • Coordinate study level investigational product arrangements and study start-up and management activities
  • Performprotocol-related site management activities
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