For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Due to expansion, we have an immediate need for an experienced Senior or Principal Coder to join or global team at ProPharma.

In this role, you will be responsible for providing data management coding support to ProPharma clients.

Key Responsibilities

• Perform accurate coding of medical terms and medications utilizing industry-wide standards as well as company standards.
• Coordinate the assignment of appropriate dictionaries for meeting study requirements.
• Performs dictionary up versions.
• Develop and maintain coding guidelines.
• Interface with colleagues from study teams across therapeutic areas on coding-related matters. Consult with Study Directors and/or Medical Monitors to resolve medical coding issues/queries.
• Participate in SAE coding reconciliation, as necessary.
• Leverage comprehensive Data Management and medical coding expertise to promote best practices across the Clinical Trial lifecycle.
• Trains and mentors coding staff, acts as a subject matter expert. 
• Provides input to ProPharma SOPs as relevant to all coding activities. 
  
  

Necessary Skills And Abilities

• Excellent communication and interpersonal skills.
  
  

Educational Requirements

• Bachelor’s degree is preferred however will accept the equivalent in years of experience.
  
  

Experience Requirements

• Required: Use of MedDRA and WHO Drug dictionaries.
• Required: Developing and maintaining coding processes and conventions.
• Required: Expertise with EDC systems, such as Medidata Rave, Merative’s Zelta system and/or Veeva EDC.
• Preferred: Working with clinical trials or within the pharmaceutical environment.
  
  

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***