Reference Number: JO-2208-498757
Clinical Site Manager
Rate: £35,700 – 71,400
Job Type: Permanent
Location: Germany, Frankfurt

Clinical Site Manager

6 month FTC

75,000- 80,000

Wiesbaden, Germany

ASAP start date

CPL Life Sciences are partnering with a global CRO who are seeking additional support on a 6-month project based in Wiesbaden, Germany. This position will be directly managing a large vaccine study having oversight of the study at site level. If you have strong knowledge of trial regulations and are available to commit to a 6 months project then this will be a fantastic role for you to make a true impact within a critical vaccine trial.

Your key responsibilities will include:

Ensure the trial is carried out in line with study protocols

Follow SOPs/WPs. Regulations and ICH-GCP

Document coordination and submission when required

Oversee patient recruitment and ensure all targets are met

Assist site performance

Site initiation and close-out when required

Ensure data entry is correct and within set timelines

Ensure correct storage of drugs and relevant trial materials

Issue resolution

Understanding of GCP processes

Provide support to more junior team members

If you have experience as a Clinical Trial Manager or Site Manager then please apply here, or send your CV to sarah.phillips@cpl.com.

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here