
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.
🔥 0 minutes ago
🌐 Serbia, Croatia, +5 more countries – Remote
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
👻 Ghost score 10%
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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.
• Independently deliver all medical support required for successful project delivery according to contracted agreements with sponsors, fulfilling all assigned tasks and timelines • Actively participate in study planning with feasibility leaders and solution consultants • Participate in team project meetings and investigator meetings • Provide training to study teams on therapeutic area indication and protocol, excluding direct medical advice on patient care or management • Participate in the development and review of study documents including clinical protocols, Medical Monitoring Plans, integrated clinical and statistical summary reports, safety plans, and Informed Consent Forms • Deliver medical monitoring activities according to Medical Monitoring Plans during study conduct • Provide medical leadership to projects in close coordination with the Project Leader, serving as either Global Lead Physician or Regional Lead Physician as assigned • Provide medical input into pharmacovigilance workflows and participate in safety processing, including medical review of serious adverse events • Support business development efforts with medical expertise • Provide medical expertise to clients across multiple channels and interactions • Offer consultancy on protocol development and drug development programs • Conduct medical review of various documents that may be audited by clients and regulatory agencies • Initiate and maintain strong medical and consultative relationships with clients • Provide expert guidance on early engagement and pre-award opportunities • Serve as a medical monitor for contracted projects • Participate in strategic initiatives, mentor junior physicians, and manage a team of medical professionals where appropriate
• Medical qualification from an acknowledged medical school • Minimum 5+ years of clinical medicine and practice experience • Qualified Psychiatrist or Neurologist, with up to date knowledge and expertise • Experience as a medical monitor, ideally from another CRO • Background in clinical aspects of drug development, including medical monitoring and study design/execution • Knowledge of the drug development process including drug safety • Experience in Pharmaceutical Medicine • Experience leading, mentoring, and managing individuals or teams • Excellent English language skills (written and spoken)
• Opportunity to work on diverse, innovative clinical research projects • Professional development and mentoring opportunities • Potential for leadership and team management roles • Competitive compensation and benefits package • Collaborative working environment with leading clinical research professionals
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