Single Sponsor Medical Director – Medical Advisor

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🇬🇧 UK Skilled Worker Visa Sponsor

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Logo of Syneos Health

Syneos Health

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Provide medical oversight of assigned clinical studies as a medical monitor • Serve as primary medical contact for customers on assigned clinical studies • Provide medical input and oversight for Drug Safety and Pharmacovigilance • Support protocol design, development, and amendments • Develop and deliver project-specific and therapeutic training to project teams and clinical site staff • Provide medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification activities • Review informed consent templates and subject-facing materials • Contribute to site feasibility evaluations • Provide medical input into data collection tools, monitoring plans, and review and analysis plans • Oversee Medical Scientist staff and Medical Director colleagues reviewing clinical data • Present clinical trends, issues, and mitigation strategies to customers and project team members • Provide after-hours medical coverage for clinical studies • Support Requests for Proposals and Bid Defense Meetings when requested • Provide input to clinical development or regulatory teams when requested • Represent the Company at scientific meetings when requested

🎯 Requirements

• Medical Director (Medical Advisor) role commutable to Reading, UK • In-depth knowledge of FDA and worldwide drug development regulations • Knowledge of national and ICH Good Clinical Practice (GCP) guidelines • Equivalent experience, skills, and/or education will also be considered • Ability to provide after-hours medical coverage for clinical studies • Ability to adhere to enterprise, customer, project, and standard operating procedures

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations, when appropriate, to assist employees or applicants to perform essential functions

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