Global Study Manager
1 day left
- Company
- CK Clinical
- 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:
Quote job ref 50202.
It is essential that applicants hold entitlement to work in the UK.
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.
- 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.
Quote job ref 50202.
It is essential that applicants hold entitlement to work in the UK.