Clinical Coder II/ Medical Coder Specialist (Sponsor Dedicated/US Based; Remote) Position Available In Jackson, Missouri

Salary Not Available Clinical Coder II/ Medical Coder Specialist (Sponsor Dedicated/US Based; Remote)
Syneos Health/ inVentiv Health Commercial LLC

Location:

Kansas City, MO – 64118
Positions available: 1
Job #: 25000290MO

Source:

FileImport – Syneos Health/ inVentiv Health Commercial LLC

Posted:

6/25/2025

Expires:

12/22/2025

Web Site:

commercialcareers.syneoshealth.com

Job Type:

Regular, Full Time (30 Hours or More) Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window. Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window.
Work Onsite
Full Time Schedule
Full Time Job Type
Regular
Job Description Help for Job Description. Opens a new window. Job Description Help for Job Description. Opens a new window.
Clinical Coder II/ Medical Coder Specialist (Sponsor Dedicated/US Based; Remote)
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. 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 accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

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 our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job ResponsibilitiesDrive Data Quality. Power Global Research. Make a Measurable Impact.
Are you a clinical coding specialist ready to elevate your impact on global clinical trials? Join our sponsor-dedicated team as a Clinical Coder II, where your expertise in medical terminology and coding will directly influence the quality, integrity, and success of innovative drug development. This is more than a coding role-it’s your opportunity to be a vital link between clinical insights and regulatory clarity. If you thrive on precision, collaboration, and seeing your work translate into real-world health solutions, this remote, full-time position was made for you.

What You’ll Do:

As a Clinical Coder II, you’ll ensure accurate, consistent, and compliant coding of clinical trial data across global studies. You’ll collaborate with data managers, medical monitors, and cross-functional teams to deliver clean, regulatory-ready datasets that help move life-saving therapies forward. Apply industry-standard coding (MedDRA, WHODrug) to adverse events, medical history, and medications across multiple studies. Conduct quality checks (QCs) and data consistency reviews using tools like Medidata RAVE Coder, TMS, and Veeva. Generate and resolve coding queries for ambiguous data and unclear terminology. Support study start-up activities, including dictionary configuration, UAT testing, and coding specifications development. Partner with global stakeholders-data management, clinical, and medical-to ensure timely, high-quality coding delivery across trials. Participate in serious adverse event (SAE) reconciliation, data transfers, and regulatory documentation reviews. Help onboard and train new team members and contribute to the development of best practices and SOPs.

What You Bring:

Education & Experience
Bachelor’s degree in health science or life sciences preferred. Equivalent experience considered. Minimum 2+ years of industry experience in clinical research, pharmacovigilance, or data management with at least 1-2 years focused on medical coding. Experience with MedDRA and WHODrug is strongly preferred. Familiarity with clinical databases and tools such as …For full information see follow application link. Help for Employer Information. Opens a new window.