Clinical Sample Coordinator AstraZeneca Gothenburg

Job description
We’re currently looking for a Clinical Sample Coordinator to join a dynamic Early Clinical Development team for a consultant assignment. 


At AstraZeneca, innovation is more than just research. As one of the world's leading pharmaceutical companies, we’re focused on providing medicines that make a real difference in patient care. Join us, and you’ll be part of a brand-new vision for a critical industry, making a difference around the globe in the process. 


The role is based within the Biosamples group in Precision Medicine and requires an understanding of laboratory testing in order to effectively manage our external laboratory suppliers. In this role, you will assist in project managing the delivery of laboratory related activities in both early and late phase global development projects. We will look to you to work closely with our internal senior team members, our global external laboratory partners / alliances and the clinical project teams to ensure operational delivery of the clinical laboratory testing of biological specimens, the efficient deployment of tests (including biomarkers, central safety and clinical bioanalysis), as well as data generation and delivery throughout the project lifecycle. This is a fantastic opportunity to play a key role in the development of an exciting portfolio of medicines that will change the lives of patients’ worldwide, working from a world-class, cutting-edge research centre.

Responsibilities
Your position will be varied and include the responsibility for ensuring all externalised laboratory activities meet internal and external quality and regulatory standards, whilst using your operational expertise to advise clinical teams on operational lab strategy, development and deployment. You will regularly be involved in providing advice to clinical teams on laboratory related documentation, operational design and new ways of working such as Case Form Reports (CRF's), Informed Consent Forms (ICF's), sample collection and distribution, as well as managing external providers to oversee the delivery of relevant lab services and data.

Qualifications
To be considered for this position it is expected that you have experience of clinical development, as well as an understanding of GCP and GCLP. In addition to this, the following experiences are desirable;
Experience of working with external partners or Alliances
Experience of working multi-nationally
Hands-on experience in a clinical laboratory setting or clinical research site
Project management experience

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-03-18, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information: Birgitta Nyström birgitta.nystrom@randstad.se or Eleonor Ehrman +46733434109. 

About the company
Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus!