Senior Clinical Research Associate

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

📋 Description

• Oversee and manage the advancement of clinical studies at investigative sites

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

• Coordinate the necessary activities to establish and oversee studies

• Identify suitable investigators

• Assist in the preparation of regulatory submissions

• Conduct pre-study and initiation visits

• Manage clinical trials of appropriate size

• Provide support to larger clinical study teams

• Train and mentor junior staff members

• Engage directly with clients

• Initiate payment processes

• Participate in proposal-related activities, including development and client presentations

⛳️ Requirements

• Bachelor's degree or equivalent experience

• Possession of a CRA certification

• At least 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device setting

• Experience in monitoring clinical trials across diverse therapeutic areas

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

• International travel may be necessary for certain senior-level roles

• Proficiency in English and the local language is essential

• Additional language skills are considered advantageous

• Graduate or postgraduate degree with a focus on a scientific or healthcare discipline is preferred

• Experience with study start-up activities is preferred

• Knowledge of financial management is preferred for Senior CRAs

🏝️ Benefits

• Employees are empowered to create a meaningful impact

• Establish meaningful client relationships

• Opportunities for career advancement

• Professional development initiatives

• A collaborative work environment

• A focus on quality in the workplace

• An emphasis on accountability within the work culture