Senior Clinical Research Associate (Dermatology)

TL;DR

Senior Clinical Research Associate (Dermatology): Managing clinical trial sites through evaluation, initiation, monitoring visits, and termination activities with an accent on GCP/ICH compliance, source data verification, and safety reporting. Focus on training site staff, resolving data queries, and ensuring high-quality, reliable clinical data for dermatology studies.

Location: Poland, Czech Republic, Bulgaria

Company

Global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies with over 4,000 professionals in 20+ countries.

What you will do

• Conduct site evaluation, initiation, monitoring, and close-out visits, including source data verification and CRF review.
• Train site staff on study procedures and ensure timely resolution of data queries and safety issues (AEs, SAEs, SUSARs).
• Act as main site contact, provide quality control support, and report activities to department head.
• Assist with study preparation, contract negotiations, and regulatory submissions as needed.

Requirements

• University degree in scientific, medical, or paramedical discipline
• Proven experience as CRA with on-site monitoring
• Previous experience in Dermatology studies
• Fluent in English and local language(s)
• Strong knowledge of clinical trial operations, GCP/ICH guidelines, and regulatory requirements
• Willingness to travel
• Proficiency in Microsoft Office

Culture & Benefits

• Supportive culture focused on professional development, continuous training, and quality delivery.
• Emphasis on diversity, inclusivity, and equal opportunities.
• Low turnover due to close management and employee-centric values.
• Mission to accelerate innovative drugs and devices for a healthier world.

Hiring process

• Submit CV for acknowledgement.
• Phone interview if shortlisted.
• No individual replies for unsuccessful applications due to high volume.