Clinical Data Reviewer - Oncology Required (US, CAN, UK Only)

First Job Previous Job 2,606 of 10,000 More Like This Salary Not Available Position range in Kansas City, MO-KS Metropolitan Statistical Area $43k

• $57k Per Year Clinical Data Reviewer
• Oncology Required (US, CAN, UK Only) Syneos Health/ inVentiv Health Commercial LLC

Occupation:

Proofreaders and Copy Markers

Location:

Kansas City, MO

• 64118

Job Type:

Full Time (30 Hours or More)

Posted:

05/16/2026 Positions available: 1

Source:

FileImport

• Syneos Health/ inVentiv Health Commercial LLC

Web Site:

commercialcareers.syneoshealth.com

Expires:

08/25/2026 Job #: 25108929MO Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window. Work Onsite Full Time Schedule Full Time Job Description Help for Job Description. Opens a new window. Clinical Data Reviewer

• Oncology Required (US, CAN, UK Only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.

We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver

• for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health
• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture
• where you can authentically be yourself. Central to this is our purpose
• Driven to Deliver
• which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities
• Industry experience with Oncology is required
• Candidates must reside in US, UK, or Canada with no sponsorship needs.

The Clinical Reviewer (CR) is a specialized role that performs clinical review, typically ahead of significant project milestones (interim analysis, study closeout, submission etc.). The studies supported by the CR are often, but not exclusively, comparative safety and efficacy (Phase 3) trials with large, multi-faceted data sets. The review tasks performed by this role include both point-to-point clinical review checks and interpretive analysis such as reviewing data for submission, highlighting errors, raising queries etc. from a clinical perspective. The CR will work as an extension of the clinician/clinical scientist and will be responsible for the clinical review of one or more studies with the ability to move easily from project to project as necessary. This requires that the CR be knowledgeable about the therapeutic area under investigation, expected effects of the investigational drug and concomitant medications, and possess sufficient clinical knowledge to assess if data is scientifically and clinically valid.

ROLE RESPONSIBILITIES

Ensure data readiness for important milestones including, but not limited to, interim analysis, final analysis, snapshots to support submissions, Data Monitoring Committee reviews and publications Review participant level data across a study in adherence with CRF Completion guidelines (CCGs) and the Data Review Plan (DRP) Conduct point-to-point data checks (e.g. verifying the presence of a lab test that satisfies study inclusion criteria) and interpretive analysis (e.g. reviewing to identify inconsistencies in the participant's data). Generate queries on discrepant data and follow to resolution including escalation of issues that cannot be resolved through the query process Create and use data review best practices and associated data review tools to identify trends and any safety signals May identify protocol deviations during routine clinical review and escalation as appropriate Follow relevant SOPs and ...For full information see follow application link.