Global Study Manager

We are currently looking for a Global Study Manager to join a leading Pharmaceutical company for an initial 12 month contract. As the Global Study Manager you will be responsible for supporting delivery of early phase global clinical studies within Oncology R&D from study set-up through maintenance, close-out and study archiving.

This is a fully remote based role, you must have full right to work in the UK without sponsorship.

Your duties as the Global Study Manager will be varied however the key duties and responsibilities are as follows:

1. As the Global Study Manager, you will perform study management tasks as per agreed delegation by the Global study Associate Director/Director

2. As the Global Study Manager, you will contribute to the preparation of study documents (e.g. Informed Consent Form, applicable study plans, etc.), and external service provider-related documents (e.g. specifications, study specific procedures, etc.).

3. As the Global Study Manager, you will maintain and facilitate interactions with functions to ensure efficient study delivery to time, costs and quality objectives.

4. As the Global Study Manager, you will lead the set-up and maintenance of third-party vendors.

To be successful in your application to this exciting opportunity as the Global Study Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in a related discipline.

2. Proven industry experience in ICH-GCP requirements, relevant regulatory/ethics requirements and clinical/drug development.

3. A working knowledge and practical experience within all phases of a clinical study lifecycle.


Key Words: Global Study Manager / Global Study Management / Clinical Trials / ICH / GCP / Good Clinical Practice / CRO / Pharmaceutical / Biotechnology