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Clinical Scientist - Immunology; Expertise in Ulcerative Colitis, Crohn's disease and Rheumatol

Job in St. Joseph, Saint Joseph, Buchanan County, Missouri, 64506, USA
Listing for: Syneos Health/ inVentiv Health Commercial LLC
Full Time position
Listed on 2026-07-08
Job specializations:
  • Science
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 80000 - 120000 USD Yearly USD 80000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn's disease and Rheumatol[...]
Location: St. Joseph

Clinical Scientist
- Immunology (Expertise in Ulcerative Colitis, Crohn's disease and Rheumatology + Excel) - Clinical Drug Trial Exp
- Must Have Job Responsibilities

  • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). 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 as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews.
  • Authors medical data queries, reviews query responses, and approves query closure in association with Medical Director.
  • May assist Medical Director in patient profile review, scientific review of other study‑level data, protocol deviation review, and creation of Medical Review Summary reports 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 project‑specific milestones and timelines are met; serves as primary interface between 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. Escalates ongoing and newly developed study concerns such as at‑risk project deliverables and out‑of‑scope tasks to the project leads in a timely manner.
  • Attends Trusted Process meetings and may participate in internal and external audits.
  • Acquires basic understanding and knowledge of ongoing protocol designs and disease‑related terminology and pathology.
  • Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs); follows all enterprise policies, standard operating procedures, work instructions, and project plans, and adheres to customer policies and standard operating procedures as required.
Salary Range

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Benefits
  • Company car or car allowance
  • Health benefits (medical, dental, and vision)
  • 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) 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.

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. In accordance with the legislation of each country in which it operates, including the implementation of the EU Equality Directive, this document fully complies with all obligations, and 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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