Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
October 29
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
• Provides medical oversight of clinical trials. • Attends and presents at investigator and sponsor meetings. • Provides medical consultation to clients, investigators and project team members. • Supports business development activities. • Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle. • Ensures tasks delegated to PVG are properly executed. • Adheres to applicable regulations and ICH guidelines regarding clinical trials. • Communicates clearly with associates and clients. • Provides therapeutic training and protocol training on assigned studies. • Contributes to departmental process improvement initiatives. • Monitors all safety variables of clinical studies. • Discusses all medical concerns with principal investigators and clients. • Performs data review as specified in the client contract and data validation manual.
• MD or equivalent required. • Active medical licensure preferred. • Board certified or eligible. • Candidates should have a combination of clinical experience and industry experience. • Therapeutic expertise across one or more medical specialty or sub-specialties. • Strong decision-making, problem solving, organizational skills and analytical skills. • Excellent oral and written communication skills. • Working knowledge of relevant safety databases (e.g. Medra). • Flexibility to travel domestically and internationally. • Ability to work independently, analyze work with attention to detail, process and prioritize sensitive complex information. • Proficiency in basic computer applications. • Fluent in spoken and written English. • Excellent interpersonal, influencing and team building skills. • Understanding guidelines (FDA, ICH, EMA and GCP). • Working knowledge of biostatistics, data management, and clinical operations procedures. • Ability to act as a mentor/trainer to other staff within PVG. • Additional experience is required for Sr Med Director level.
Apply NowOctober 28
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Lead medical management for Centene's diverse member population.
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Oversee quality and utilization management for early childhood support services.
🇺🇸 United States – Remote
💵 $105.2k - $178.9k / year
💰 $101M Private Equity Round on 2004-01
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director