Senior Clinical Research Associate

Senior Clinical Research Associate I

Remote with on-site visits

Location: Poland

Are you ready to gain valuable experience in innovative clinical research across various therapeutic areas? We are seeking talented candidates for a role that offers a unique opportunity to collaborate with sponsor (one of the best known pharmaceutical company) in FSP model.

Key Responsibilities:

• Protocol Review & Site Visits: Thoroughly review approved protocols and ensure that qualification, initiation, monitoring, and closeout visits for research sites are executed with complete compliance.
• Study Integrity & Compliance: Maintain the highest integrity of the study, ensuring strict adherence to guidelines, protocols, and regulations.
• Monitoring & Reporting: Compile detailed monitoring reports and follow-up letters, highlighting significant findings, deviations, deficiencies, and recommending actions to ensure compliance.
• Team Collaboration: Play an active role in the project team by providing insightful feedback and innovative suggestions for the successful completion of the project.
• Mentorship: Coach and mentor less experienced CRAs, contributing to their development and training.

What We're Looking For:

• University degree in life sciences, pharmacy, or biotechnology;
• At least 3 years of independent monitoring experience (including pre-study, initiation, routine monitoring, and close-out visits) according to protocol monitoring guidelines, SOPs, and GCP/ICH Guidelines;
• Good IT skills (use of MS Office, and various clinical IT applications on computer, tablet, and mobile devices) and the ability to adapt to new IT applications on various devices;
• Ability to understand and analyze data/metrics and act appropriately;
• Fluent command of English;
• Excellent communication skills, including the ability to understand and present technical information effectively;
• Ability to complete tasks accurately and in a timely manner

Join us and advance your career in a dynamic and inspiring research environment! Your expertise and dedication can help shape the future of patient’s treatment.

To show that you are appreciated in our team, while working at KCR Placement you will be provided with:

• 1 additional day off for your birthday;
• Private medical healthcare;
• Loyalty Bonus Program (anniversary awards or additional paid time off);
• Additional days off during the end of the year;
• Employee referral system;
• Onboarding process and induction training to develop deep sector knowledge and complex skills;
• Latest technology and the most advanced equipment and working tools;
• An open culture based on slim processes, in an agile structure with a flat hierarchy and direct access to the Management to share ideas and implement change and continuous improvement;
• Mentoring and training programs related to clinical trials, therapeutic areas, hard and soft skills.

Learn more about KCR Placement:

KCR Placement operates as a full-service recruitment services provider, placing high-quality talents in the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe.

Our Employees are KCR Placement's most crucial asset. We commit to placing our candidates at the center of all we do and setting them up for long-term career development and success. Our Employees receive attractive benefits in compliance with all national regulations. We are proud of providing excellent working conditions and a dynamic work atmosphere.

KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.

If you require reasonable accommodations to participate in the application process, please let us know by email: eeo@kcrcro.com. We are committed to ensuring equal opportunity for all applicants and will work to provide reasonable accommodations to support your needs.

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