
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.
🔥 19 hours ago
🌐 United States, Canada – Remote
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
👻 Ghost score 10%
Where this job comes from
Posted on Syneos Health's careers page, not through a job board
First seen by Remote Rocketship 19 hours ago
Still open on Syneos Health's site. Checked 2 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.
• Provides medical oversight of assigned clinical studies as a medical monitor • Serves as primary medical contact for customers for assigned clinical studies • Provides medical input and oversight supporting Drug Safety and Pharmacovigilance • Supports protocol design and development and provides input into protocol amendments • Develops and delivers project-specific and therapeutic training to project team members and clinical site staff • Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts • Reviews Informed Consent Templates and Subject-Facing Materials and contributes to site feasibility evaluations • Provides medical input into data collection tools, monitoring plans, and review and analysis plans • Oversees Medical Scientist staff and Medical Director colleagues reviewing clinical data • Presents identified trends, issues, and mitigation strategies to customers and project teams • Provides after-hours medical coverage for clinical studies • Adheres to enterprise, customer, project, and regulatory policies and procedures • May support Requests for Proposals and Bid Defense Meetings • May provide input to clinical development or regulatory teams • May represent the Company at scientific meetings
• Must be located in the United States • Board-certified in Ophthalmology is required • Doctorate degree in medicine • Clinical experience in the practice of medicine in the specific therapeutic area • Clinical research experience required • In-depth knowledge of FDA and worldwide drug development regulations • Strong understanding of medical terminology and drug names in multiple nations and environments • Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and voicemail • Effective organizational, interpersonal, communication, language, and group presentation skills • Above-average attention to detail and accuracy • Ability to handle multiple tasks and meet deadlines in a dynamic environment • Customer-focused and disciplined approach to work • Fluency in written and spoken English is essential • Up to 25% travel may be required
• 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
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
🔥 21 hours ago
Clinical drug safety leader supporting Centessa’s orexin medicines for narcolepsy and sleep-wake disorders. Driving signal management, aggregate reports, ICSR oversight, and pharmacovigilance compliance.
🇺🇸 United States – Remote
💵 $117k - $189.2k / year
💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🔥 21 hours ago
Senior Director leading global Medical Information strategy, operations, and transformation at Jazz Pharmaceuticals. Advancing scientific content, customer engagement, analytics, and digital capabilities across therapeutic areas.
🇺🇸 United States – Remote
💵 $224k - $336k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
🕒 Yesterday
Medical Affairs leader shaping lung cancer strategy and evidence generation at Jazz Pharmaceuticals, a global biopharma company. Guiding early oncology pipeline development and cross-functional scientific planning.
🇺🇸 United States – Remote
💵 $268k - $402k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
🕒 Yesterday
Global Medical Director leading breast cancer medical strategy, evidence generation, and scientific engagement for Jazz Pharmaceuticals’ oncology portfolio. Partnering across regional and global biopharma teams.
🇺🇸 United States – Remote
💵 $268k - $402k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
🕒 Yesterday
Global Medical Director guiding GI oncology evidence strategy for Jazz Pharmaceuticals’ cancer medicines. Aligning regional Medical Affairs teams, clinical development, and global commercialization.
🇺🇸 United States – Remote
💵 $268k - $402k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor