Early Phase Oncology CRA - UK

This role would suit a CRA who has a strong background in oncology studies, ideally including P I and II work. This role will be more than a standard monitoring role; you will be asked to be involved in a far wider range of responsibilities and be able to influence the study process as it goes on. As a result, applicants with an academic grounding within oncology would be at a distinct advantage.

 

Responsibilities:

Designing, implementing and monitoring clinical studies;

Supervising and conducting external clinical studies, and liaising with technical staff and investigators at universities, hospitals and other medical facilities;

Preparing and reviewing clinical documentation which ensures that clinical studies meet customer needs;

Scheduling studies and communicating results in a timely manner to meet business needs;

Creating and delivering training to external investigators and study site coordinators;

Representing ADC at external meetings and conferences;

Providing supervision, coaching and mentoring to other members of the team;

Providing clinical input to new product development projects.

 

Requirements:

Degree educated the science/health care field or nursing degree or equivalent

Experience in monitoring clinical trials within a commercial setting

Experience within the oncology therapy area

Must have valid, current driver’s license

 

This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be.

 

To make an application please feel free to apply via this website, I am also available on LinkedIn to message regarding the role and will accept all invitations that refer to this advert - look for Dominic Mitchell at RBW Consulting.

 

Please note that owing to the high volume of applications we receive for our roles, if you have not received a response within 48 working hours, do please consider your application unsuccessful.

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