Job Description:
• Encode terms reported as adverse events and medical history, as well as prior and concomitant medications, using industry-accepted dictionaries such as MedDRA and WHODrug
• Perform coding according to 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:
• Bachelor’s degree or related health science background
• Commensurate experience considered in lieu of a 4-year degree
• 2+ years 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
• Excellent written and oral skills
• Ability to work independently and within cross-functional teams
• Strong attention to detail and commitment to high-quality work
• Working knowledge of coding tools such as Medidata RAVE Coder, TMS, and Veeva
Benefits:
• Career development and progression
• Supportive and engaged line management
• Technical and therapeutic area training
• Peer recognition and total rewards program
• 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) and sick time
• Company car or car allowance may be included