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Syneos Health

Medical Coding Specialist – Clinical Coder II

Syneos Health

. Encode terms reported as adverse events and medical history, as well as prior and concomitant medications, using industry-accepted dictionaries such as MedDRA and WHODrug .

Posted 9/21/2026full-timeRemote • United StatesJuniorMid-Level💰 $56,400 - $95,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in pharmacovigilance and clinical data management, with a strong focus on coding using MedDRA and WHODrug. Proficient in medical terminology and committed to maintaining high-quality standards in data processing and collaboration.

Highest-signal resume keywords
Pharmacovigilance ExperienceMedDRA CodingWHODrug CodingClinical Data ManagementAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data CodingMedical TerminologyClinical Trials KnowledgeCoding ConventionsAdverse Event Reporting
Soft Skills
Excellent Written SkillsExcellent Oral SkillsAbility to Work IndependentlyCollaboration Skills
Tools & Technologies
Medidata RAVE CoderTMSVeeva
Industry Keywords
Clinical ResearchCoding ToolsSOPsData Consistency ReviewsSAE Reconciliation

About the role

Key responsibilities & impact
  • Encode terms reported as adverse events and medical history, as well as prior and concomitant medications, using industry-accepted dictionaries such as MedDRA and WHODrug
  • Perform coding according to departmental coding conventions and company SOPs
  • Generate queries to clarify potentially discrepant data
  • Assist with data coding consistency reviews and SAE reconciliation as needed
  • Collaborate with medical monitors and Clinical and Data Management team members to ensure timely processing according to project timelines
  • Assist in interdepartmental training of new staff as needed

Requirements

What you’ll need
  • Bachelor’s degree or related health science background
  • Commensurate experience considered in lieu of a 4-year degree
  • 2+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management
  • Experience with MedDRA and WHODD preferred
  • Working knowledge of medical terminology, clinical trials, and coding
  • Excellent written and oral skills
  • Ability to work independently and within cross-functional teams
  • Strong attention to detail and commitment to high-quality work
  • Working knowledge of coding tools such as Medidata RAVE Coder, TMS, and Veeva

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • 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) and sick time
  • Company car or car allowance may be included