Senior Clinical Research Associate I

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

📋 Description

• Independently oversee and track designated investigational sites throughout the complete study lifecycle.

• Ensure adherence to ICH-GCP, regulatory standards, and internal quality benchmarks.

• Conduct Site Initiation Visits, Monitoring Visits, and Close-Out Visits, both onsite and remotely.

• Establish and nurture trustworthy relationships with investigators and study personnel.

• Assist in patient recruitment, study initiation, and maintaining data quality.

• Identify and address study-related issues while implementing corrective and preventive measures.

• Support audits and inspections along with quality improvement initiatives.

• Mentor and offer subject-matter expertise to Clinical Research Associates.

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a related field (e.g., nursing, pharmacy, or a medical background).

• Minimum of 3 years of experience in clinical monitoring.

• Oncology experience is preferred, along with familiarity with other therapeutic areas such as vaccines, internal medicine, or infectious diseases.

• Extensive knowledge of ICH-GCP and both national and international regulatory requirements.

• Experience with global clinical trials.

• Proficient in both written and spoken German and English.

• Strong communication, organizational, and problem-solving capabilities.

• Willingness to travel approximately 60–80% within Germany and, when necessary, internationally.

• Valid driver’s license and passport are mandatory.

🏝️ Benefits

• Pfizer ensures equal opportunities throughout the entire application process.

• An inclusive employer dedicated to providing equal opportunities for all applicants.

• Reasonable accommodations are available for applicants and future careers.

• Accessibility support for the website, online application process, and interviews.