Clinical/Medical Scientist – Medical Monitoring, Infectious Disease, HIV

🔥 0 minutes ago

🏈 Alabama, Alaska, +38 more states – Remote

infoinfo

💵 $67.7k - $115.1k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

infoinfo

👻 Ghost score 0%

infoinfo
Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

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

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 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 visualizations • Analyze data to identify risks and patterns/trends and document medical reviews • Proactively 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 among internal teams, customers, and vendors for medical data and eligibility review • Collaborate with study teams to identify risks to data integrity and subject safety • 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 • Adhere to data privacy, ICH, GCP, company, customer, and project requirements

🎯 Requirements

• Medical/scientific expertise relevant to infectious disease and HIV • Understanding of ongoing protocol designs and disease-related terminology and pathology • Experience performing medical review of clinical data listings and data visualizations • Ability to analyze data to identify risks and data patterns/trends • Ability to author medical data queries and review query responses • Knowledge of medical plans, patient profile review, scientific study-level data review, and protocol deviation review • Knowledge of medical data review and safety review meetings • Ability to manage project scope, objectives, deliverable quality, milestones, and timelines • Ability to collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management • Adherence to data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, and project plans • Equivalent experience, skills, and/or education may be considered

🏖️ 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 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

Apply Now

Similar Jobs

🕒 5 days ago

Agilent Technologies

10,000+ employees

🍽️ Food & Beverage

🏥 Healthcare

💼 Consulting

Clinical Affairs Scientist advancing clinical evidence for oncology companion diagnostics at Agilent, a global laboratory and clinical technology company. Supporting trials, regulatory submissions, and scientific marketing.

🇺🇸 United States – Remote

💵 $105.3k - $197.4k / year

💰 $500M Post-IPO Debt on 2019-09

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

infoinfo

🕒 August 13

Baylor Genetics

501 - 1000

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Clinical genomics scientist analyzing WGS data and curating variants for Baylor Genetics clinical reports. Supporting genomic test validation, evidence assessment, and laboratory R&D technology development.