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TMF Specialist

rhoworldRemote — Poland
Remote Full-time

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Experience Level

Experience

Qualifications

Proven experience in clinical research or a related field. Thorough understanding of TMF processes and regulatory requirements. Excellent communication and interpersonal skills. Strong organizational abilities and attention to detail. Proficient in document management systems and Microsoft Office Suite.

About the job

rhoworld seeks a TMF Specialist to support clinical research projects from a remote location in Poland. The position centers on managing and maintaining Trial Master Files (TMFs) to satisfy regulatory standards.

What you will do

  • Maintain and organize TMF documentation at every stage of the clinical trial process
  • Verify that TMFs remain accurate, complete, and compliant with industry regulations
  • Collaborate with cross-functional teams to address documentation needs for clinical trials

What we value

  • Keen attention to detail
  • Strong organizational abilities
  • Dedication to high standards in clinical research

About rhoworld

rhoworld is a leading organization in the clinical research sector, dedicated to innovation and quality. We pride ourselves on fostering a collaborative and inclusive work environment that empowers our employees to thrive. Our commitment to professional development and growth ensures that our team is equipped with the tools and knowledge to succeed.

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