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Job Description
- Req#: 120037
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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