(Senior) CRA, Poland
Education and Experience:
• Degree in pharmacy, life science or related field;
• Ideally 2 or more years of monitoring experience in interventional
studies with a CRO, pharmaceutical or biotech company.
Additional Requirements:
• Demonstrated clinical trial monitoring skills;
• In-depth understanding of ICH/GCP guidelines;
• Excellent standard of verbal and written communication skills in
English language;
• Highly organized with strong attention to detail and deadlines;
• Advanced skills across all of the MS Office packages;
• Willingness to travel.
As an equal opportunity employer, PPD believes that employees are the key to
its success, and is committed to your professional growth. We offer an
attractive salary, comprehensive benefits package as well as bespoke personal
development and training programs.
Only shortlisted candidates will be contacted. For more information, please,
feel free to visit our corporate web site at: www.ppdi.com.