Clinical Study Administrator - Hybrid - Warsaw - Poland - FSP

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP offers you the security of a long-term position and many opportunities for career progression. We are currently recruiting talented and passionate people to join our FSP teams in Poland. Parexel FSP offers you the security of a long-term position and many opportunities for career progression. We are currently recruiting talented and passionate people to join our FSP teams in Poland. The Clinical Study Administrator position 3 days weekly office based in Warsaw gives you the opportunity to join a team with a wide range of experience and expertise. Position Purpose: The Clinical Study Administrator (CSA) will assist in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Primary Duties: Trial and site administration and support. Document Management (eTMF, ISF). Regulatory & Site Start-Up responsibilities. Budgeting, Agreements and Payments. Skills and Education: High school/Secondary school qualifications (or equivalent adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers. Further studies in administration and/or in the life science field are desirable . +2 years previous administrative experience in clinical trials industry, CRO or big pharma required. Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH-GCP guidelines. Proven organizational and administrative skills. Computer proficiency. Proficient in written and spoken English language required. Fluency in local language(s) required. Ability to develop advanced computer skills to increase efficiency in daily tasks. Good verbal and written communication. Good interpersonal skills and ability to work in an international team environment. Willingness and ability to train others on study administration procedures. Excellent organization and time management skills. Excellent attention to detail. Ability to multi-task in a high-volume environment with shifting priorities. Team oriented and flexible; ability to respond quickly to shifting demands and opportunities. Integrity and high ethical standards. We will offer you Premium salary. Attractive benefits. Medical care plan: Health, Dental & Vision. Life Assurance. Excellent work environment. Culture of teamwork and collaboration. People who motivate and face challenges together. Innovative technology. Excellent training. Base Pay Range for Poland: PLN 96,000 - 105,000 Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location. In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and total rewards incentives. Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. Join a global community where you can transform your career into a life-changing achievement. Apply directly or contact us via email at