Medical Scientist, ONC – Bladder Late Phase

🔥 12 hours ago

🏈 Alabama, Arizona, +38 more states – Remote

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💵 $67.7k - $139.6k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

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👻 Ghost score 0%

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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

• Work with the Medical Director to develop Medical Management, Medical Data Review, and Eligibility Review Plans • Engage outside experts, consultants, and advisors to obtain medical/scientific input for medical plans • Perform regular and ad-hoc medical review of data listings and data 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 study teams to identify data integrity and subject safety risks • Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads • Participate in internal and external audits • Participate in or conduct interviews

🎯 Requirements

• 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, ICH, GCPs, enterprise policies, standard operating procedures, work instructions, and project plans • Adherence to customer policies and standard operating procedures, as required in project plans • Ability to work with medical data review, eligibility review, data listings, and data visualization • Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management • Ability to participate in or conduct interviews • Ability to participate in internal and external audits

🏖️ Benefits

• 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 401(k) • 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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