Senior Clinical Research Associate

This is a fully remote position, open to applicants in Germany, +4 more countries.

📋 Description

• Oversee and take responsibility for the progression of clinical studies at investigation sites.

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

• Coordinate necessary activities to establish and monitor studies.

• Identify and engage investigators.

• Assist in preparing regulatory submissions.

• Conduct pre-study and initiation visits.

• Manage appropriately scaled clinical trials.

• Provide support to larger clinical study teams.

• Train and mentor junior team members.

• Engage directly with clients.

• Initiate payment processes.

• Participate in proposal 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 in a CRO, pharmaceutical, biotechnology, or medical device setting.

• Experience in monitoring clinical trials across various therapeutic areas.

• Willingness to travel domestically, including overnight stays, with an approximate commitment of 50–60% travel.

• International travel may be necessary for some senior-level roles.

• Proficiency in English and the local language.

• Additional language skills are considered a plus.

• Graduate or postgraduate degree in a scientific or healthcare field is preferred.

• Experience in study start-up activities is preferred.

• Familiarity with financial management is preferred, particularly for Senior CRAs.

🏝️ Benefits

• Fully remote position within Germany.

• Opportunities for professional development.

• Chance to cultivate meaningful client relationships.

• Opportunities for career advancement.

• Employee empowerment to create an impact.