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Syneos Health

Clinical Coder II

Syneos Health

. Encode terms reported as adverse events and medical history .

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 adverse events and medications using MedDRA and WHODrug. Proficient in collaborating with cross-functional teams to ensure data accuracy and compliance with industry standards.

Highest-signal resume keywords
Pharmacovigilance ExperienceMedDRA CodingClinical Data ManagementMedidata RAVE CoderAttention 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
Adverse Event CodingMedical TerminologyClinical Trials KnowledgeData Coding Consistency ReviewsSAE Reconciliation
Soft Skills
Excellent Written SkillsExcellent Oral SkillsAbility to Work IndependentlyCollaboration Skills
Tools & Technologies
MedDRAWHODrugMedidata RAVE CoderTMSVeeva
Industry Keywords
Clinical ResearchCoding ConventionsSOPsCross-Functional TeamsInterdepartmental Training

About the role

Key responsibilities & impact
  • Encode terms reported as adverse events and medical history
  • Encode prior and concomitant medications using industry-accepted dictionaries such as MedDRA and WHODrug
  • Perform coding in accordance with 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, or commensurate experience in lieu of a four-year degree
  • 2+ years of 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
  • Working knowledge of coding tools such as Medidata RAVE Coder, TMS, and Veeva
  • Excellent written and oral skills
  • Ability to work independently and within cross-functional teams
  • Strong attention to detail and commitment to high-quality work

Benefits

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