Clinical Research Associate II

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

📋 Description

• This position is primarily focused on training and development, providing support and observation of clinical site monitoring services both in-house and in the field while enhancing CRA skills and knowledge.

• The role offers exposure and training in all facets of clinical site monitoring services, while performing monitoring and site management activities for full-service studies to ensure compliance with protocols, SOPs, and regulatory standards.

• Responsibilities include managing sites to promote investigator site and patient recruitment, compliance, and oversight.

• Conduct remote data reviews, assist with data queries and closure activities, support Risk-Based Monitoring (RBM) efforts, evaluate data collection and regulatory document gathering, and carry out remote and on-site activities for investigational sites, including site contacts, qualification, initiation, monitoring, and closeout visits under supervision or independently, in accordance with corporate, sponsor, and regulatory (ICH GCP and others) standards and guidelines.

• The position represents the corporation by fostering collaborative relationships with stakeholders.

⛳️ Requirements

• The ideal candidate will hold a college diploma or degree and have 1-3 years of relevant experience.

• Certifications such as SoCRA, CCRA, and/or ACRP are considered advantageous.

• The successful applicant must demonstrate self-motivation, strong communication skills, and a dedication to achieving positive outcomes.

• A keen attention to detail and an understanding of the significance of building collaborative relationships to achieve results is essential.

• A commitment to ongoing learning and self-improvement is required.

• The ability to continuously promote teamwork is necessary.

🏝️ Benefits

• Home-based work arrangement.

• Regular travel opportunities.