Clinical Medical Scientist – Medical Monitoring, Infectious Disease

🔥 2 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

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Syneos Health

WebsiteLinkedInAll Job Openings

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

• Develop medical plans with the Medical Director, including Medical Management, Medical Data Review, and Eligibility Review Plans • Coordinate acquisition of medical/scientific input from outside experts, consultants, and advisors • Perform regular and ad-hoc medical review of data listings and visualizations • Analyze data to identify risks and 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 reviews, 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 among internal teams, customers, and vendors for medical data and eligibility review • Collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management 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 internal and external audits • Maintain understanding of protocol designs, disease terminology, and pathology • Follow data privacy guidelines, ICH, GCPs, company policies, SOPs, work instructions, and project plans

🎯 Requirements

• Degree in life sciences (BS, MSc, PharmD, PhD) • Medical monitoring experience in HIV clinical trials required • Excellent time management skills to handle multiple tasks and meet deadlines in a highly regulated and dynamic environment • Self-starter comfortable with fluctuating timelines, work demands, and changes in scope of work • Ability to troubleshoot situations and escalate issues or questions when needed • Understanding of scientific principles for effective, high-quality medical data analysis • Excellent written and oral communication skills • Excellent computer skills, including MS Office programs, spreadsheets, and presentations • Knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines • Strong interpersonal skills and ability to work effectively in a cross-functional team environment • May travel up to 25%

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • 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 • Company car or car allowance may be included