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Senior Medical Coding Specialist

PRA Health Sciences

Canada

On-site

CAD 80,000 - 110,000

Full time

16 days ago

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Job summary

A leading clinical research organization is looking for an expert in clinical data coding to join their team. In this role, you will be responsible for coding clinical study data, ensuring quality checks, and collaborating with cross-functional teams. Ideal candidates should hold a Bachelor's degree in health science, have a robust background in medical terminology, and at least five years of experience in the industry, including coding responsibilities.

Benefits

Comprehensive health insurance
Flexible optional benefits
Global Employee Assistance Programme
Career advancement opportunities
Commitment to work-life balance

Qualifications

  • Minimum of 5 years in pharmacovigilance, clinical research, or data management.
  • 4 years of coding experience is required.
  • Experience with MedDRA and WHODD is essential.

Responsibilities

  • Code clinical data for in-house studies and generate queries.
  • Perform quality checks and collaborate with clinical teams.
  • Troubleshoot operational issues with coding tools.

Skills

Medical terminology
Coding experience
Communication skills

Education

Bachelor's degree in health science

Job description

Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary with a range of additional benefits
- Opportunity for career advancement and growth within a diverse and inclusive culture
- Comprehensive health insurance offerings to suit you and your family’s needs
- Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships
- Global Employee Assistance Programme providing 24-hour access to support for you and your family’s well-being
- Commitment to work-life balance and well-being opportunities

What to Expect (Job Responsibilities):
- Code clinical data for all in-house studies and generate coding queries for inadequate data or unclear medical terms
- Review coding documentation related to study start-up documents and coding specifications
- Identify and troubleshoot operational issues with coding tools; liaise with vendors to ensure timely coding activities
- Perform quality checks and data reviews to ensure coding consistency
- Collaborate with medical monitors and clinical teams to ensure timely processing of coding according to project timelines

What is Required (Qualifications):
- Bachelor’s degree in health science or equivalent experience
- Minimum of 5 years of industry experience in pharmacovigilance, clinical research, or clinical data management, including 4 years of coding experience
- Expertise in medical terminology and coding is essential
- Excellent written and oral communication skills with the ability to work independently and in cross-functional teams
- Experience with MedDRA and WHODD is required

How to Stand Out (Preferred Qualifications):
- Experience in Oncology is a plus

#ClinicalResearch #MedicalCoding #HealthcareCareers #DiversityAndInclusion #CareerGrowth

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