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Clinical Trial Assistant (CTA) at Biomapas
Kaunas, Kaunas County, Lithuania -
Full Time

Start Date

Immediate

Expiry Date

19 Apr, 26

Salary

1500.0

Posted On

19 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Trials, Attention To Detail, Time Management, Organizational Skills, Communication Skills, Microsoft Office, CTMS, Quality Check, Financial Reporting, Documentation Management

Industry

Research Services

Description
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 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 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
Responsibilities
The Clinical Trial Assistant supports the project team in the start-up, execution, and close-out of clinical trials. Responsibilities include maintaining study files, assisting with financial reports, and organizing trial documentation.