Quality & Training Advisor

PRA international

Place of work
Hungary, Poland, Sweden
Contract type
full-time

Information about the position

Job description, responsibilities and duties

As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

At PRA, borders do not create boundaries. PRA's success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages - yet operate in unison as one worldwide PRA community.

This is an exciting new role which offers the opportunity for an experienced clinical research professional to utilise their training and development skills in the training of others.

Working fully outsourced to and based at the offices of our global pharmaceutical client, the Quality and Training Advisor will take responsibility for on boarding and training of all new clinical employees (CRA's, CTA's and CTM's) across Europe. Working as part of a Global Training group and in conjunction with Training colleagues in America's and Asia Pacific you will coordinate and run the initial three month induction programme which includes training in process, systems and SOP's in order to ensure standardised on boarding across the region. In addition, you will also be involved in the monitoring and analysis of regional quality metrics.

Requirements for the employee

Candidates with education suit the position

Secondary with school-leaving examination

Language skills

English - Intermediate (B1)

Personality requirements and skills

The successful candidate for this role will be able to demonstrate prior experience as a Clinical Research Associate or Clinical Team Manager within either a pharmaceutical company or a CRO environment in addition to experience within Quality, Training and Complance. Prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. Fluency in English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively.

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Brief description of the company

PRA is a top five CRO that has worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

At PRA, borders do not create boundaries. PRA's success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages - yet operate in unison as one worldwide PRA community.
ID: 2138614  Dátum zverejnenia: 15.6.2015