
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.
🔥 10 minutes ago
🏈 Alabama, Arizona, +38 more states – Remote
💵 $79.8k - $139.6k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Work with the Medical Director to develop medical plans, including Medical Management, Medical Data Review, and Eligibility Review Plans • Engage outside experts, consultants, and advisors to coordinate necessary medical/scientific input • Perform regular and ad-hoc medical review of data listings and data visualizations • Analyze data to identify risks and data patterns/trends and document medical reviews • Identify and resolve medical data review issues • Author medical data queries, review responses, and approve query closure with the Medical Director • Assist with patient profile reviews, scientific review of study-level data, protocol deviation review, and Medical Review Summary reports • Partner with Medical Directors on medical data review and safety review meetings, including slide preparation • Manage project scope, objectives, deliverable quality, milestones, and timelines • Serve as primary interface between internal teams, customers, and vendors for medical data and eligibility review • Collaborate with study teams to identify data integrity and subject safety risks • Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads • Attend and present at Trusted Process meetings and participate in audits • May manage a limited number of direct reports and participate in or conduct interviews
• Equivalent experience, skills, and/or education will also be considered • Basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology • Adherence to data privacy guidelines, International Committee on Harmonization (ICH), Good Clinical Practices (GCPs), enterprise policies, standard operating procedures, work instructions, and project plans • Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management • Ability to manage project scope, objectives, quality of deliverables, milestones, and timelines • Ability to attend and present at Trusted Process meetings and participate in internal and external audits • Medical data review and eligibility review experience implied by the listed responsibilities • Oncology and GYN therapeutic-area knowledge implied by the role title and responsibilities
• career development and progression • supportive and engaged line management • technical and therapeutic area training • peer recognition and total rewards program • Inclusive culture • 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) and sick time
Apply Now🔥 1 hour ago
Senior Clinical Scientist leading oncology clinical trials for ICON’s sponsor-dedicated research programs. Providing medical monitoring, scientific oversight, and protocol execution across US and Canadian locations.
🔥 8 hours ago
Senior Clinical Data Management leader overseeing non-interventional studies for Kite’s cancer immunotherapy programs. Driving data integrity, regulatory readiness, vendors, timelines, and cross-functional delivery.
🇺🇸 United States – Remote
💵 $143.2k - $185.3k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 8 hours ago
Clinical data management leader overseeing Kite’s non-interventional and investigator-sponsored studies. Supporting cancer immunotherapy development through CDM strategy, compliance, vendors, and cross-functional delivery.
🇺🇸 United States – Remote
💵 $143.2k - $185.3k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 11 hours ago
Associate Director advancing Otsuka’s pharmaceutical drug development through AI, machine learning, biomarkers, and real-world data. Leading GenAI solutions, analytics, and evidence generation across R&D.
🔥 20 hours ago
Clinical Study Manager leading pre-market and post-market medical-device trials for Intuitive’s robotic-assisted surgery technologies. Driving protocols, monitoring, regulatory submissions and evidence generation.
🇺🇸 United States – Remote
💵 $128.9k - $218.3k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor