Clinical Research Associate, Dermatology (Contract, Poland, Home based) - IQVIA Biotech

IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. We're looking for Independent professionals who are willing to work from home with an international EU team. IQVIA Biotech specialises in working with smaller biotech and emerging biotech and Med tech clients and as such we have a vibrant, fast-paced work environment. You’ll be working with a lot of the new innovative and upcoming research groups across a variety of therapy areas. Here at Iqvia Biotech we place a real emphasis on: work life balance and employee progression, with a real focus and developing career paths

The Clinical Research Associate / Senior Clinical Research Associate is responsible for the monitoring of clinical trials and tracking of study progress, thereby contributing to the overall management of clinical trials in accordance with the appropriate quality standards including ICH-GCP guidelines, Standard Operating Procedures (SOPs), applicable regulations, rules and guidance.

KNOWLEDGE, SKILLS AND ABILITIES:
•Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
•Experience in monitoring and/or coordinating clinical trials required.
•Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
•Demonstrated ability to form strong functional relationships.
•Excellent, presentation, organizational and interpersonal skills.
•Ability to interact with all levels of staff to coordinate/execute study activities.
•Ability to handle several priorities within multiple, complex trials.
•Ability to reason independently and recommend specific solutions in clinical settings.
•Ability to work independently, prioritize, and work within a matrix team environment.
•Ability to mentor other CRAs and co-monitor, as required.
•Knowledge of electronic data capture including basic data processing functions.
•Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research

Ability to travel weekly to clinical sites as needed.