
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.
🔥 17 hours ago
🏄 California, Illinois, +2 more states – Remote
💵 $146k - $332k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Syneos Health's careers page, not through a job board
First seen by Remote Rocketship 17 hours ago
Still open on Syneos Health's site. Checked 3 hours ago.

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.
• Provide medical oversight of assigned clinical studies as Medical Monitor • Provide therapeutic input and consultation to customers for assigned clinical studies • Develop and deliver project-specific and therapeutic training to project team members and clinical site staff • Provide training to customer staff as needed • Provide medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts • Review Informed Consent Templates and subject-facing materials • Provide input into site feasibility evaluations • Support protocol design and development and provide input into protocol amendments • Provide medical input into data collection tools, monitoring plans, and review and analysis plans • Oversee assigned Medical Scientist staff and Medical Director colleagues reviewing clinical data • Present identified trends and issues, with mitigation strategies, to customers and project teams • Provide after-hours medical coverage for clinical studies • Provide input to clinical development or regulatory teams upon request • Collaborate with internal stakeholders and customers during the pre-sales process when needed • Represent the Company at scientific meetings when requested • Adhere to enterprise policies, work instructions, standard operating procedures, project plans, and applicable customer policies and procedures • Maintain knowledge of FDA and worldwide drug-development regulations and national and ICH Good Clinical Practice (GCP) guidelines
• Board certification in Dermatology is indicated by the job title • In-depth knowledge of FDA and worldwide drug-development regulations • Knowledge of national and ICH Good Clinical Practice (GCP) guidelines • Ability to provide after-hours medical coverage for clinical studies • Equivalent experience, skills, and/or education may be considered
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Company car or car allowance • Medical, Dental and Vision health benefits • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) • Sick time
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