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PPD

CRA, Client-dedicated, Poland

PPD is a leading global contract research organization providingcomprehensive, integrated drug development, laboratory and lifecycle managementservices. Our customers include pharmaceutical, biotechnology, medical device,academic and government organizations. With offices in 46 countries andapproximately 23,000 professionals worldwide, PPD applies innovativetechnologies, therapeutic expertise and a firm commitment to quality to help customersbend the cost and time curve of drug development and optimize value indelivering life-changing therapies to improve health.

PPD has an exciting opportunity for aCRA to join us and work exclusively for one of our strategic pharmaceuticalpartners in Poland. As part of the PPD services to this partner, you will bededicated to client-specific projects and sites, collaborating with the client'steams under some of their systems and processes.

Clinical Research Associate (Client onsite), Poland

This is a great opportunity for CRAsat any level currently working within the life science sector forpharmaceutical companies, biotech companies or CROs who would enjoy theopportunity to work for one client. You should thrive in project teams and befocused on delivering exemplary levels of customer service. You will haveexcellent communication and interpersonal skills and are looking to work in acollegiate environment where you want to take true ownership for your work. Youwill perform and coordinate all aspects of the clinical monitoring process. Youshall also be qualified to conduct monitoring activities independently.

*LI-MP1

Job Qualification:

Education and Experience:

• University degree in a science related field.

• At least 1 year independent monitoring experience in clinical development phase II-IV.

• Understanding of ICH-GCP, EU and FDA requirements

• Fluency in English and in Polish

• Valid Driver's License where applicable

• Proven clinical monitoring skills

• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology

• Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures

• Good oral and written communication skills, with the ability to communicate effectively with medical personnel

• Good organizational and time management skills

• Ability to work in a team or independently as required

• Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software

Our offer: In return we will offer you a positive and supportive working environment within one of the most engaged teams in the industry; who are truly recognised as the cornerstone of our success. We will provide you with meaningful work and the opportunity to acquire valuable personal and professional skills.

Please submit your CV in English.

Registration on our website will also give you the opportunity to be considered for other positions if this one is not the most appropriate for your qualifications and experience.

Only short-listed candidates will be contacted.

PPD is an equal opportunities employer.

Diversity Statement

PPD is proud to be an affirmative action employer that values diversity as a strength and fosters an environment of mutual respect. PPD is committed to providing equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual orientation, disability, veteran status or status within any other protected group.

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