Senior Clinical Research Associate

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TFS HealthScience

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Clinical Research Excellence

CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting

501 - 1000

Description

• Conduct all stages of site monitoring • Monitor on-site and remotely clinical trials • Review CRFs and subject source documentation for validity and accuracy • Identify site problems/deficiencies and report them to management • Initiate corrective actions to resolve issues • Contribute to the completion of applications to Ethics Committees/IRBs

Requirements

• Bachelor’s Degree, preferably in life sciences or nursing, or equivalent • Minimum 1-3 years of relevant clinical experience • Ability to work in a fast-paced environment with changing priorities • Understanding of basic medical terminology and science related to the assigned drugs and therapeutic areas • Familiarity with Good Clinical Practice regulations and ICH guidelines • Ability to work independently as well as in a team-oriented environment • Excellent written and verbal communication skills in English and Polish

Benefits

• Competitive compensation package • Comprehensive benefits • Personal and professional growth opportunities