Parexel Clinical Research Physician Recruitment 2026: Apply Online

About the Role

Parexel is seeking a dedicated and experienced Clinical Research Physician to join our Early Phase Clinical Unit (EPCU) in Berlin, Germany. This is a critical role where you will contribute significantly to the advancement of medical research by acting as a co-investigator on Phase I and II studies. Your primary responsibility will be to ensure the safety of trial participants at all times, while also supporting the Principal Investigator in the meticulous preparation, organization, conduct, and reporting of clinical trials. Adherence to protocol, Standard Operating Procedures (SOPs), ICH-GCP, and local regulations is paramount.

This position offers flexibility in terms of working hours, with options for full-time (40 hours) or part-time (30 hours) employment. The role may involve morning, afternoon, and occasional night shifts, as well as availability for weekend shifts, depending on the dynamic needs of the business.

Key Accountabilities

• Clinical Trial Management: Provide comprehensive support to the responsible Principal Investigator and Deputy PI, ensuring all activities align with national and international laws and applicable guidelines. You will be responsible for the conduct of assigned studies, coordinating and supporting medical activities, and upholding medical responsibility. Strict compliance with German Drug Law, local laws, study guidelines, and SOPs is mandatory.
• Departmental Support: Contribute to the Medical Operations Department’s objectives by supporting duties that ensure performance is met or exceeded, aligning with both business goals and your own personal objectives.
• Personal Development: Actively participate in your own Personal Development Process, focusing on continuous learning and professional growth.
• Process and Data Quality: Engage in process and data quality optimization initiatives to enhance the efficiency and reliability of clinical trial operations.
• Emergency Preparedness: Participate in required emergency training within the Medical Operations department to ensure readiness for any eventuality.
• Sponsor Interaction: Participate in medical and scientific discussions with sponsors via teleconference and meetings at the study level. Engage with external specialists and attend Sponsor meetings as required during the course of studies.
• Documentation and Reporting: Contribute to the writing of medical reports, publications, SOPs, and work instructions, ensuring clarity and accuracy.
• Team Environment: Maintain a positive, results-oriented work environment, fostering open, balanced, and objective communication within the team.

Skills and Qualifications

• Education: University degree as a medical doctor, including approbation.
• Clinical Research Knowledge: Profound understanding of clinical research principles, applicable German/European guidelines and laws, and ICH GCP.
• Language Proficiency: Superior English and German language skills (verbal and written) are mandatory.
• Technical Skills: Proficiency in computer skills, including MS Office and MS Outlook.
• Interpersonal Skills: Excellent peer and patient relationship management abilities. High interpersonal, verbal, and written communication skills.
• Problem-Solving: Strong clinical and ethical problem-solving capabilities.
• Client Focus: A client-focused approach to work, understanding and meeting the needs of sponsors and stakeholders.
• Adaptability: A flexible attitude towards work assignments and a commitment to continuous learning.
• Workload Management: Ability to manage multiple tasks effectively and prioritize workload with enthusiasm and attention to detail.
• Certifications: Advanced Life Support (ALS) trained and updated.

Parexel is a leading global clinical research organization (CRO) dedicated to helping the world’s pharmaceutical and biotechnology companies accelerate the development of new medicines and therapies. With a focus on patient-centricity and scientific excellence, Parexel provides a comprehensive suite of services across the drug development lifecycle, from early-phase research to late-stage clinical trials and regulatory affairs. The company is committed to innovation, quality, and collaboration, striving to improve patient outcomes and bring life-changing treatments to market faster.