Clinical Trial Assistant (CTA)

Kaunas , Lithuania
full-time

AI overview

Assist with all administrative tasks in clinical trials while ensuring compliance and maintaining key documentation and quality standards.

Join our global team as a Clinical Trial Assistant (CTA) in Lithuania, in Kaunas Office.

Clinical Trial Assistant is responsible for all administrative tasks and assists the project team in the start-up, execution and close-out of the trial.

Responsibilities:

  • Support of Clinical Operation and Start-up activities
  • Maintain study files and perform regular quality check
  • Support with investigators payment, project financial reports preparation
  • Maintain various systems and platforms used in clinical trials
  • Operational support for Clinical Operations department
  • Assist Clinical Research Associate and Project Manager on clinical trial related activities
  • Organize clinical trial documentation and files oversight

Requirements

  • University degree, preferable Life Science related field
  • Effective written and verbal communication skills including good command of English language
  • Experience in Clinical Trials is an advantage
  • Computer skills including proficiency in use of Microsoft Office, CTMS and other clinical trial related systems and platforms
  • Attention to detail and ability to manage competing priorities
  • Effective time management and organizational skills

Benefits

  • Professional growth and career opportunities
  • International team and environment
  • Bonus based on annual performance
  • Personal accident and business trip insurance
  • Additional health insurance payment
  • Influenza vaccines
  • Rewarding referral policy
  • Team building, global meetings, B active events

Salary range 1200-1500 eur/gross/month

Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.

View all jobs
Salary
€1.200 – €1.500 per month
Report this job
Apply for this job