Medical Director – Study Physician

🔥 17 hours ago

🇦🇹 Austria – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Serve as the medically responsible physician at the trial level throughout preparation, conduct, and reporting of clinical trials • Provide medical expertise and medical oversight from the Trial Design Outline through the Clinical Trial Report • Join the core trial team • Work dedicated to one client • Ensure timely preparation of high medical quality clinical trial protocols while minimizing protocol amendments • Contribute to trial risk-based quality management by defining medically relevant data and ensuring related risks are integrated into the quality and risk management plan • Co-author Clinical Quality Monitoring plans • Perform ongoing reviews of medical data • Collaborate with a key sponsor in the EMEA region

🎯 Requirements

• Physician (MD), ideally with medical thesis • Trained in a clinical setting • Minimum of 4 years of active clinical practice experience • Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine highly desirable • Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions / any other relevant medical function, ideally in Clinical Development, desirable • Understanding of relevant regulations and guidance including ICH-GCP • Ideally previous experience as a medical monitor • Ideally experienced with data visualization systems and IT systems • Clinical development/trials experience is an additional asset • Must be based in Austria for this Austria-Remote role

🏖️ Benefits

• Premium salary • Attractive benefits • Medical care plan: Health, Dental & Vision • Life Assurance • Pension plan • Excellent work environment • Culture of teamwork and collaboration • Innovative technology • Excellent training • Opportunity to join a global community and transform your career