Clinical Study Administrator — Growth & Training in Warsaw

Parexel; Poland; On-site; PLN 96,000 - 105,000; Full time

Benefits offered by this job

Premium salary

Attractive benefits

Health, Dental & Vision plan

Life Assurance

Excellent training

Job summary

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 will coordinate study activities from start-up to close-out within the Local Study Team to ensure quality, cost control and timeliness. The role includes trial and site administration, document management, regulatory start-up tasks and budgeting.

Qualifications

• High school/Secondary school qualifications; adapted to local market needs.
• Further studies in administration and/or life sciences desirable.
• 2+ years administrative experience in clinical trials, CRO or pharma.
• Knowledge of Clinical Study Process and ICH-GCP guidelines.

Responsibilities

• Trial and site administration and support.
• Document Management (eTMF, ISF).
• Regulatory & Site Start-Up responsibilities.
• Budgeting, Agreements and Payments.

Skills

Administrative experience

English proficiency

Team collaboration

Excellent organization

Written communication

Education

High school diploma

Life sciences administration studies

Tools

Computer proficiency

Job description

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 will coordinate study activities from start-up to close-out within the Local Study Team to ensure quality, cost control and timeliness. The role includes trial and site administration, document management, regulatory start-up tasks and budgeting.