Join our International Team

We are always keen to meet ambitious, creative individuals who want to make a difference. If you are interested in applying for one of the positions below or would like to work for WEP Clinical in another capacity, then please contact us at:

Expanded Access Manager – London, UK

The ideal candidate should be an experienced Project Manager and will be accountable for the setup, implementation, and delivery of Expanded Access Programs for Pharmaceutical and Biotech Companies.

Role Objectives

The EAP Manager will be the primary point of contact for clients, managing all aspects of the delivery of the project as well as providing advice and guidance. This is a pivotal role and requires a strong customer focus and attention to detail as well as the ability to develop and execute project plans, track against KPIs, identify risk and contingency planning.

Expanded Access Manager – Morrisville, NC, USA

The ideal candidate should be an experienced Project Manager and will be accountable for the setup, implementation, and delivery of Expanded Access Programs for Pharmaceutical and Biotech Companies.

Role Objectives

The EAP Manager will be the primary point of contact for clients, managing all aspects of the delivery of the project as well as providing advice and guidance. This is a pivotal role and requires a strong customer focus and attention to detail as well as the ability to develop and execute project plans, track against KPIs, identify risk and contingency planning.

Clinical Research Associate I/II (CRA I/II) – MORRISVILLE, NC, USA

The Clinical Research Associate I/II (CRA I/II) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and WEP Clinical Standard Operating Procedures.

Role Objectives

This position requires proven monitoring skills. The CRA I/II conducts site visits to assess site adherence to protocol and regulatory requirements as well as manages required documentation. The CRA I/II will also be responsible for ensuring the data remains audit ready and able to pass an audit by WEP Clinical, the Sponsor or a regulatory agency.

Join our International Team

We are always keen to meet ambitious, creative individuals who want to make a difference. If you are interested in applying for one of the positions below or would like to work for WEP Clinical in another capacity, then please contact us by clicking the link below:

Expanded Access Manager – London, UK

The ideal candidate should be an experienced Project Manager and will be accountable for the setup, implementation, and delivery of Expanded Access Programs for Pharmaceutical and Biotech Companies.

Role Objectives

The EAP Manager will be the primary point of contact for clients, managing all aspects of the delivery of the project as well as providing advice and guidance. This is a pivotal role and requires a strong customer focus and attention to detail as well as the ability to develop and execute project plans, track against KPIs, identify risk and contingency planning.

Expanded Access Manager – Morrisville, NC, USA

The ideal candidate should be an experienced Project Manager and will be accountable for the setup, implementation, and delivery of Expanded Access Programs for Pharmaceutical and Biotech Companies.

Role Objectives

The EAP Manager will be the primary point of contact for clients, managing all aspects of the delivery of the project as well as providing advice and guidance. This is a pivotal role and requires a strong customer focus and attention to detail as well as the ability to develop and execute project plans, track against KPIs, identify risk and contingency planning.

In-house Clinical Research Associate I/II (CRA I/II) – Morrisville, nc, usa

The In-house Clinical Research Associate I/II (CRA I/II) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and WEP Clinical Standard Operating Procedures.

Role Objectives

This position requires proven monitoring skills. The CRA I/II conducts site visits to assess site adherence to protocol and regulatory requirements as well as manages required documentation. The CRA I/II will also be responsible for ensuring the data remains audit ready and able to pass an audit by WEP Clinical, the Sponsor or a regulatory agency.

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