Clinical Scientist, Medical Monitoring – Oncology, Multi-Indication

🔥 18 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• 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 obtain medical/scientific input • Perform regular and ad-hoc medical review of data listings and data visualizations • Analyze data to identify risks and patterns/trends and support documentation of medical reviews • 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 the 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 project concerns, at-risk deliverables, and out-of-scope tasks to project leads • Attend Trusted Process meetings and participate in internal and external audits • Adhere to applicable data privacy, ICH, GCP, company, customer, and project requirements

🎯 Requirements

• Knowledge of ongoing protocol designs and disease-related terminology and pathology • Adherence to data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs) • Adherence to enterprise and customer policies, standard operating procedures, work instructions, and project plans • Equivalent experience, skills, and/or education will also be considered • Ability to work with medical data review, eligibility review, data listings, and data visualization • Ability to author medical data queries and review query responses • Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management teams

🏖️ Benefits

• 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 • Reasonable accommodations when appropriate