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Site Activation Specialist

Central London   •  Negotiable  •  Contract/Temporary, Full time


Site Activation Specialist
6 month initial contract
Remote: UK, Spain or Belgium
Offering 40-50 per hour DOE
(Inside IR35 for the UK)

Cpl Life Sciences are actively seeking a number of Site Activation Specialists to join a global CRO for an initial 6 month contract. This position will be focusing on the site identification and initiation, liaising directly with the regulatory team to ensure site activation is completed effectively and efficiently. Our client has a growing portfolio and is therefore recruiting across Europe within the UK, Spain and Belgium.

Key responsibilities will include:
- Site identification and initiation activities
- Central and local Ethic Committee submissions
- Authority submissions
- Investigator and site contract management
- Ensure all site activation documentation is completed to schedule
- Ensure GCPs are followed to the highest standard
- Comply with SOPs, ICH GCP and national regulations as applicable
- Contribute to budget and time management

Previous experience:
- Pharma/CRO experience
- Site activation/feasibility responsibilities
- Ethic Submissions
- Full understanding on the regulations required
- Awareness of ICH GCP Guidelines and the FDA/ EU Clinical Trials Directives/National regulations
- Proficient in both spoken and written English
- Self motivated
- Positive attitude and strong communication skills
- Proficient in Microsoft Office

Our client are looking for someone to start as soon as possible, so if you are immediately available or on a short notice then this would be ideal for you.

If this position is of interest then please apply or send your CV directly to sarah.phillips@cpl.com.

  • Agency: Cpl Life Sciences
  • Contact: Sarah Phillips
  • Reference: JO-2102-461977
  • Posted: 3rd February 2021
  • Expires: 3rd March 2021

Cpl Life Sciences

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