Clinical Research Associate

Company Overview

Precision Medicine Group specializes in oncology and rare diseases, focusing on precision medicine through innovative clinical trial designs and advanced data analytics. They foster a supportive and engaging work environment with notably high retention rates among Clinical Research Associates (CRAs).

Role Summary

The CRA role involves managing one to two clinical studies, allowing you to become an expert in clinical trial protocols with reasonable travel commitments that support a healthy work-life balance. Working here means having your contributions valued and directly influencing study outcomes within a smaller CRO setting.

Candidate Profile

• Maintains composure and responsiveness during unexpected challenges.
• Thoroughly prepares for site visits, meetings, and team updates, anticipating needs ahead of time.
• Employs creative problem-solving methods to overcome obstacles.
• Demonstrates keen attention to detail in all tasks.
• Identifies risks within studies and suggests effective mitigation strategies.
• Assumes responsibility for the quality and results of their work.
• Skilled at resolving conflicts using established resolution techniques.

Key Responsibilities

• Monitor and oversee clinical trials at investigative sites ensuring adherence to protocols, SOPs, ICH-GCP, and applicable regulations.
• Coordinate all activities necessary for study initiation and monitoring including investigator identification, regulatory submissions support, and conducting study visits.

Minimum Requirements

• A graduate or postgraduate degree in a scientific or healthcare-related field.
• At least one year’s experience as a CRA in a CRO or pharmaceutical/biotech setting, or equivalent clinical research experience such as site management.

Additional Qualifications

• Strong communication and organizational capabilities with a collaborative team spirit.
• Demonstrated client-oriented approach.
• Willingness to travel domestically up to 50-60%, including overnight stays; international travel may be needed for senior roles.
• Proficiency in English and German.
• Experience in oncology, CAR-T therapies, or first-in-human phase III clinical trials.

Preferred Experience

• Expertise in study start-up procedures.
• Familiarity with medical device clinical trials.

Additional Information

Applicants should apply in English. The company is committed to equal opportunity employment and encourages individuals with disabilities to request reasonable accommodations during the application process. They warn against recruitment fraud and provide contact information for reporting suspicious activities. All application data is handled in accordance with privacy policies.