Performing site selection, initiation, monitoring and close-out visits
Supporting the development of a subject recruitment plan
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Collaborating with experts at study sites and with client representatives

Requirements

University Degree in life science or other scientific discipline or apprenticeship in health care
Minimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
Strong experience in monitoring of clinical trials
Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
Good command of Polish and English language
Flexibility to travel

Benefits

Resources that promote your career growth
Leaders that support flexible work schedules
Programs to help you build your therapeutic knowledge
Dynamic work environments that expose you to new experiences
Home-office, company car, and more

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

site selectionmonitoringsubject recruitment plan developmentregulatory submissions trackingcase report form (CRF) completiondata query resolutionclinical trials monitoring

Soft skills

strong written communicationstrong verbal communicationattention to detailability to work in a fast pace environmentflexibility to travel

Certifications

Good Clinical Practice (GCP)International Conference on Harmonization (ICH)