Senior Specialist, Clinical Coding (Remote)

Talentify.io; United States; Remote; USD 60,000 - 100,000; Full time

Job summary

An innovative company in the pharmaceutical industry is seeking a coding expert to join their remote team. This role offers the opportunity for career advancement and a comprehensive benefits package, including medical, dental, and vision insurance. As a primary coding resource, you will play a crucial role in clinical trials, ensuring accurate data coding and contributing to the company's goals. If you have a health science background and proficiency in MedDRA and WHODrug, this is your chance to make a positive impact on health while working from anywhere in the U.S.

Benefits

Paid Time Off

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Short-term Incentive Programs

Qualifications

• Bachelor's degree with a health science background required.
• Proficiency in MedDRA and WHODrug is essential.

Responsibilities

• Serve as the primary coding resource for assigned studies.
• Accurately code clinical trial data using MedDRA and WHODrug.

Skills

MedDRA

WHODrug

Medical Terminology

Problem-Solving Skills

Communication Skills

Education

Bachelor’s Degree in Health Science

Tools

Clinical Trial Data Systems

EDC Coding Tools

Job description

Employer Industry: Pharmaceutical and Biotechnology

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)
- Eligible for short-term incentive programs
- Work remotely anywhere within the U.S.
- Be part of a company committed to innovation and making a positive impact on health

What to Expect (Job Responsibilities):
- Serve as the primary coding resource for assigned studies, acting as a subject matter expert for study team members and stakeholders
- Accurately code clinical trial data using MedDRA and WHODrug in accordance with company conventions
- Perform all Clinical Coding Team workflow requirements throughout the life of the trial
- Support the identification of prohibited medications and related exclusionary data
- Contribute to the development and timely achievement of company projects and goals

What is Required (Qualifications):
- Bachelor’s degree with a related health science background (e.g., RN, BSN, RPh)
- Working knowledge of medical and medication terminology
- Proficiency in MedDRA and WHODrug
- Familiarity with clinical trial data systems and/or EDC coding tools
- Effective problem-solving and communication skills

How to Stand Out (Preferred Qualifications):
- Demonstrated ability to work independently as well as in a team environment

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