Senior Clinical Research Associate

This is a fully remote position, open to applicants in Kentucky, +3 more states.

📋 Description

• Identify, select, initiate, and finalize investigational sites for phase II-IV clinical trials.

• Independently and proactively establish and oversee studies.

• Complete reports and maintain accurate documentation.

• Submit protocols and consent documents for ethics/IRB approval.

• Prepare regulatory submissions.

• Manage sponsor-generated queries effectively.

• Ensure study cost efficiency is maintained.

• Prepare and review study documentation and feasibility studies for new proposals.

• Potentially assist in the training and mentoring of fellow CRAs.

• Support sponsor-dedicated trials in Dermatology & Rare Diseases.

⛳️ Requirements

• Minimum of 18 months of monitoring experience in phase I-III trials as a CRA.

• A college degree in medicine, science, or a related field.

• Prior monitoring experience in medium-sized studies, including start-up and close-out phases.

• Knowledge of ICH-GCP guidelines and capability to review and assess medical data.

• Exceptional written and verbal communication skills in both German and English.

• Ability to meet tight deadlines.

• Willingness to travel at least 60% of the time, both internationally and domestically, by air and car.

• Valid driving license required.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.