
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.
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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.
• Serve as the Global Clinical Lead and medical monitor for one or more studies, including participation on clinical subteams • Contribute directly to protocols, clinical study reports, study documents, regulatory documents, and external publications • Review clinical trial data and medically monitor clinical trials • Interact with senior management regarding data presentations, trial updates, and executional or strategic development issues • Contribute to clinical development strategy and indication prioritization • Oversee and coordinate operational aspects of ongoing projects with clinical operations to meet time, cost, and quality expectations • Ensure Clinical Development SOPs support effective clinical research programs and comply with clinical, medical, and industry standards • Review and contribute to regulatory documents and interactions as needed • Participate in eligibility form reviews, protocol deviation teams, cross-functional safety review teams, study teams, and clinical subteams • Initiate and maintain medical and consultative client relationships and advise on early engagement and pre-award efforts • Participate in initiatives, mentor junior medical directors, and where appropriate manage a team of physicians
• MD required • Residency training in psychiatry required • Extensive drug development experience in psychiatry, particularly Phase 1–3 clinical development • Experience in schizophrenia, bipolar disorder, ADHD, and major depressive disorder indications • 5 or more years of pharmaceutical industry experience in a clinical development role such as Medical Director or Senior Medical Director • Outstanding written and verbal communication skills, including experience presenting to senior management and external audiences • Ability to manage complexity and ambiguity in a highly matrixed work environment • Strong leadership and collaborative interpersonal skills • Ability to work independently, prioritize tasks efficiently, and meet expected time frames • Ability to perform thorough reviews of medical and trial-related documents in a timely manner
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