Clinical Research Associate II

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

📋 Description

• Oversee and manage the progress of clinical trials at investigative sites, ensuring that these studies are conducted, documented, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all relevant regulations and standards.

• Coordinate all essential activities needed to establish and monitor a study, which includes identifying investigators, assisting in the preparation of regulatory submissions, and conducting pre-study and initiation visits.

⛳️ Requirements

• A graduate or postgraduate degree focused on a scientific or healthcare discipline.

• A minimum of 2.5 years of experience as a Clinical Research Associate (CRA) within a Contract Research Organization (CRO) or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies. Experience in site management or a related area in clinical research is also acceptable.

• Strong communication and organizational skills are vital. Must be a team player.

• Proven track record of a client-focused approach.

• Willingness to travel domestically, including overnight stays, which may require a travel commitment of approximately 50-60% (international travel may be necessary for some senior-level positions).

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

🏝️ Benefits

• Private medical insurance.

• MultiSport Card.

• Life insurance.

• Pension plan.

• Home working allowance.

• Vacation time.

• Discretionary annual bonus.