Clinical Research Associate II

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

📋 Description

• Oversee and take responsibility for the advancement of clinical trials at research sites.

• Ensure that clinical trials are executed, documented, and reported in accordance with the protocol, SOPs, and ICH-GCP standards.

• Organize all essential activities necessary for the setup and monitoring of a study, including identifying investigators, aiding in the preparation of regulatory submissions, and conducting pre-study and initiation visits.

⛳️ Requirements

• A graduate or postgraduate degree with a focus in a scientific or healthcare field.

• A minimum of 25 months of experience as a CRA in either a CRO or the pharmaceutical/biotech industry, or a comparable role.

• Experience in site management or a related field within clinical research.

• Strong communication and organizational abilities.

• Demonstrated commitment to a client-focused approach.

• Willingness to travel domestically, including overnight stays, with a possible commitment of approximately 50-60% travel.

• Proficiency in English, and for positions in non-English speaking countries, fluency in the local language.

• Experience with oncology studies is advantageous.

• Familiarity with study startup activities is preferred.

🏝️ Benefits

• Private medical insurance.

• MultiSport Card.

• Life insurance.

• Pension plan.

• Home working allowance.

• Paid vacation.

• Discretionary annual bonus.