Sr Medical Scientist - Immunology; Rheumatology

Syneos Health/ inVentiv Health Commercial LLC

Edmond, OKFull-timePosted Apr 13, 2026

79.8K a year

Behavioral Health Market Context

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Benefits

Health InsurancePaid Time OffDental Coverage

Job Description

 prepare the respective medical plans.
• Performs regular and ad‑hoc medical review of data listings and data visualizations, analyzes the data to identify risks and data patterns or trends, and supports documentation of medical reviews; pro‑actively identifies and resolves medical data review issues as they arise.
• Authors medical data queries and reviews query responses, approving query closure in association with the Medical Director.
• May assist the Medical Director in patient profile reviews, scientific reviews of other study‑level data, protocol deviation reviews, and the creation of the Medical Review Summary report as needed.
• Partners with Medical Directors for medical data review meetings and safety review meetings, including slide preparation as needed.
• Manages project scope of work, objectives, and quality of deliverables to ensure the project‑specific milestones and timelines are met; serves as the primary interface between the internal team, customers, and vendors in the areas of medical data review and eligibility review.
• Collaborates with study team members—including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management—to identify risks related to data integrity and subject safety, escalating ongoing and newly developed study concerns such as at‑risk project deliverables or out‑of‑scope tasks to the project leads in a timely manner.
• Attends and presents at Trusted Process meetings and may participate in internal and external audits.
• Acquires a basic understanding of ongoing protocol designs, disease‑related terminology, and pathology.
• Adheres to all data privacy guidelines, International Conference on Harmonisation (ICH), Good Clinical Practices (GCPs), enterprise policies, standard operating procedures, work instructions, and project plans; and adheres to customer policies and SOPs as required in project plans.
• May manage a limited number of direct reports and may participate or conduct interviews.
Benefits

The benefits for this position may include a company car or car allowance, health benefits to include medical, dental and vision coverage, a company match 401(k), eligibility to participate in an Employee Stock Purchase Plan, eligibility to earn commissions/bonuses based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.

Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range: $79,800.00 - $
Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.

Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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Qualifications

    Benefits

    • The benefits for this position may include a company car or car allowance, health benefits to include medical, dental and vision coverage, a company match 401(k), eligibility to participate in an Employee Stock Purchase Plan, eligibility to earn commissions/bonuses based on company and individual performance, and flexible paid time off (PTO) and sick time
    • Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work
    • Syneos complies with all applicable federal, state, and municipal paid sick time requirements
    • Salary Range: $79,800.00 - $

    Responsibilities

    • Works with the Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan) and engages with outside experts, consultants, and advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans
    • Performs regular and ad‑hoc medical review of data listings and data visualizations, analyzes the data to identify risks and data patterns or trends, and supports documentation of medical reviews; pro‑actively identifies and resolves medical data review issues as they arise
    • Authors medical data queries and reviews query responses, approving query closure in association with the Medical Director
    • May assist the Medical Director in patient profile reviews, scientific reviews of other study‑level data, protocol deviation reviews, and the creation of the Medical Review Summary report as needed
    • Partners with Medical Directors for medical data review meetings and safety review meetings, including slide preparation as needed
    • Manages project scope of work, objectives, and quality of deliverables to ensure the project‑specific milestones and timelines are met; serves as the primary interface between the internal team, customers, and vendors in the areas of medical data review and eligibility review
    • Collaborates with study team members—including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management—to identify risks related to data integrity and subject safety, escalating ongoing and newly developed study concerns such as at‑risk project deliverables or out‑of‑scope tasks to the project leads in a timely manner
    • Attends and presents at Trusted Process meetings and may participate in internal and external audits
    • Acquires a basic understanding of ongoing protocol designs, disease‑related terminology, and pathology
    • Adheres to all data privacy guidelines, International Conference on Harmonisation (ICH), Good Clinical Practices (GCPs), enterprise policies, standard operating procedures, work instructions, and project plans; and adheres to customer policies and SOPs as required in project plans
    • May manage a limited number of direct reports and may participate or conduct interviews


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