Overview

Reference Number: JO-2104-466161
Study Management Associate
Rate: Negotiable
Job Type: Contract
Location: Cambridge

Study Management Associate
11 month contract
Remote based
Day rate: £350-400 DOE

One of our leading biotech clients are in need of an experienced trial manager to join their welcoming team on an initial 12-month contract. The position will be working on a global Oncology study and involve vendor and data management. 
This position will be suitable for someone with Clinical Trial Management experience across the UK or ideally the EU/Globally. Oncology experience is essential for this role.

Key responsibilities: 
•    Support the Study Lead with various aspects of trial management and execution
•    Participate in the management of clinical study sites across the UK and a selection of other countries  
•    Review and negotiate budgets and key contracts
•    Ensure the study is completed within budget and to strict timelines
•    Ensure compliance with SOP’s, ICH/GCP guidelines and all relevant regulatory bodies 
•    Develop and review relevant documentation such as informed consent forms and study manuals
•    Assist with data collection, review as well as database lock
•    CRO/vendor management
•    Support internal audits and inspections

Key experience: 
•    Oncology experience is essential.
•    Participated in Clinical Trial Management across the UK and ideally exposure to EU or global studies.
•    Vendor management of CRO’s or worked within a CRO environment.
•    Experience within a phase II or III trial 
•    Able to plan and execute clinical trials in line with budget, timelines, and regulations.
•    Able to work independently while working remotely.
•    Strong team player and communicator 

If this role is of interest to you then please apply or send your CV to sarah.phillips@cpl.com for further information.

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