Senior Clinical Research Associate

This is a fully remote position, open to applicants in Poland.

📋 Description

• You will be assigned exclusively to a single client.

• You will oversee all site management and supervisory tasks for the designated oncology studies.

• You will collaborate with industry leaders and subject matter experts.

• You will have the chance to mentor junior Clinical Research Associates (CRAs).

• You will utilize cutting-edge technology.

• You will enjoy significant opportunities for travel, remote work, networking, and playing a vital role in the drug development process.

⛳️ Requirements

• Extensive background in site management, coupled with a solid understanding of clinical trial methodology and terminology.

• At least 2 years of experience in independently monitoring various types of site visits.

• A minimum of 2 years’ experience in independent site monitoring specifically in oncology.

• Strong time management, organizational, interpersonal, and problem-solving skills, with the capacity to multitask and prioritize effectively.

• A comprehensive understanding and practical knowledge of clinical research, clinical trial phases, current GCP/ICH regulations, and country-specific clinical research legislation and guidelines.

🏝️ Benefits

• Competitive salary

• Attractive benefits package

• Company car or car allowance

• Medical care plan covering Health, Dental & Vision

• Life Assurance

• Supportive work environment

• Culture emphasizing teamwork and collaboration

• Colleagues who inspire and tackle challenges together

• Access to innovative technology

• Comprehensive training opportunities