Global Study Manager

1 day left

Location
Cambridge
Salary
£400 per day LTD
Posted
24 Mar 2021
Closes
23 Apr 2021
Ref
50202
Contact
Julie Marshall
Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)
CK Group are recruiting for a Global Study Manager to join a company in the Pharmaceutical industry at their site based in Saffron Walden on a contract basis for 12 months. The role is working from home initially and then on site 3-4 days per week.

Company:
Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK.

Location:
This Global Study Manager role will be based at our clients site in Saffron Walden.

Salary:
£400 per day LTD.

Global Study Manager Role:
  • Perform study management tasks as per agreed delegation/oversight.
  • In partnership with internal experts and external service providers, provide oversight to ensure study delivery of both internally-run and outsourced studies.
  • Lead/contribute to the preparation of delegated study documents (e.g. Informed Consent Form, applicable study plans, etc.), and external service provider-related documents (e.g. specifications, study specific procedures, etc.).
  • Maintain and facilitate interactions with both internal & external functions to ensure efficient study delivery to time, costs and quality objectives.
  • Manage the set-up and maintenance of third-party vendors.
  • Support with budget management. Initiate contract/budget requests for third-party vendors, facilitate generation of purchase orders, track spend against approved budget and manage the change order process.
Your Background:
  • University degree (or equivalent) in medical or biological science or discipline with clinical research.
  • Relevant pharmaceutical industry and/or clinical trial experience.
  • Deep understanding of ICH-GCP, relevant regulatory/ethics requirements and clinical/drug development.
  • Proven organisational and time management skills as well as excellent attention to detail.
  • Demonstrated ability to work well both on a cross functional team and independently.
  • Experience in all phases of a clinical study lifecycle.
Apply:
Quote job ref 50202.

It is essential that applicants hold entitlement to work in the UK.

Apply for Global Study Manager

Already uploaded your CV? Sign in to apply instantly

Apply

Upload from your computer

Or import from cloud storage

Your CV must be a .doc, .pdf, .docx, .rtf, and no bigger than 1MB


4000 characters left

Marketing Communication

We'd love to send you information about Jobs and Services from PharmiWeb.jobs by email.

All emails will contain a link in the footer to enable you to unsubscribe at any time.


When you apply for a job we will send your application to the named recruiter, who may contact you. By applying for a job listed on PharmiWeb.jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please email us.

Similar jobs

Similar jobs