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Reference: JT-896218
Job Summary:
We are urgently in need of a Clinical Research Associate - CRA.

Key Responsibilities

Ensures the integrity of clinical data and adherence to applicable regulatory, protocol and Company guidelines.
Ensures the rights, safety and wellbeing of clinical trial subjects is maintained.
In accordance with COMPANY SOPs, performs site management activities including:
site evaluation visits
site initiation visits
monitoring visits
closeout visits
Collaborates with the Core Project Team to drive subject recruitment
Establishes and maintains regular contact with Investigators, vendors and trial sites to ensure compliance with applicable regulations and the protocol.

Essential Skills

BSc (or equivalent) in a life science or healthcare discipline, pharmacy degree or nursing qualification experience of monitoring clinical trials in the pharmaceutical/CRO or biotechnology industry.
Experience of monitoring clinical trials in the pharmaceutical/CRO or biotechnology industry is required where no BSc or equivalent qualification is held.
Ability to drive and be available for extensive travel including overnight stays, as required.
Possess strong verbal and written communication, interpersonal and organisational skills.
Have a high degree of accuracy and attention to detail.
Able to use initiative and problem solve.
Flexible and adaptive approach to work.
Able to work in a team and as an individual.
Ability to identify issues and resolve appropriately with guidance.


To apply for this position please send an up to date version of your CV