
Clinical Research Associate – Poland, Warsaw, Lodz, Trojmiasto, Koszalin, Szczecin, Poznan, Bydgoszcz
Posted Oct 22

Posted Oct 22
This is a fully remote position, open to applicants in Poland.
• Serve as a Clinical Research Associate dedicated to a sponsor.
• Execute all site management and oversight tasks for assigned oncology studies.
• Support clinical studies from a home office located in Poland or the relevant region.
• Collaborate with industry leaders and subject matter experts.
• Provide mentorship to junior Clinical Research Associates.
• Utilize advanced technology.
• Engage in travel, network with new individuals, and play a role in the drug development process.
• Oversee sites and protocols within the designated studies.
• Significant experience in site management, coupled with a solid understanding of clinical trial methodology and terminology.
• At least 1 year of experience in independent site monitoring across all types of visits.
• A background in science is essential.
• Must be willing to work on oncology trials.
• Strong time management, organizational, and interpersonal skills are required.
• Proficient problem-solving abilities, with the capacity to handle multiple tasks and prioritize effectively.
• A good grasp and practical knowledge of clinical research.
• Familiarity with clinical trial phases.
• Current knowledge of GCP/ICH standards.
• Understanding of local clinical research regulations and guidelines.
• Competitive salary.
• Attractive benefits package.
• Vehicle or vehicle allowance.
• Comprehensive medical care plan: Health, Dental & Vision.
• Life Assurance.
• Exceptional work environment.
• Culture that promotes teamwork and collaboration.
• Colleagues who inspire and tackle challenges collectively.
• Access to innovative technology.
• Outstanding training opportunities.
• Annual performance-based bonus plan for eligible positions.
• Annual salary review for eligible positions.
• Total rewards incentives for qualifying roles.
• Long-term career development opportunities.
• Possibilities to grow within the role, take on additional responsibilities, or enhance skills in related Parexel FSP departments.
• Opportunities for travel.
• Flexibility to work from home.
ICON plc
ICON plc
ICON plc
Worldwide Clinical Trials
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