Clinical Research Associate

An exciting clinical opportunity has arisen for a Clinical Research Associate (CRA) to work from Taiwan. You will be working fully embedded within one of our pharmaceutical clients, you'll be at the heart of our client's innovation.

Job Responsibilities

Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan. Developing effective relationships with investigator site staff to ensure that key clinical metrics are met. Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. May provide direct supervision, training and/or mentorship to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned.

Skills and Requirements

Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment is essential. A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. You will be educated to degree level in a life science discipline or be a licensed healthcare professional. Experience working on Oncology trials or complex studies would be an advantage for this role. Study start up experience (Feasibility, Contract Negotiation, submissions) preferred.

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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