Clinical Trials Medical Coder — MedDRA/WHO Coding

DaMar Staffing; Cambridge (MA); On-site; USD 60,000 - 85,000; Full time

Job summary

Integrated Resources, Inc is seeking a Medical Coder in Cambridge, MA to conduct centralized coding activities using MedDRA and WHO Drug dictionaries, supporting clinical trials and pharmacovigilance.

You will work with the Study Management Team, CDPM and CP to align coding targets with study timelines, review adverse event coding with SABR physicians, and ensure accuracy across in-house and outsourced trials. Experience in data management or safety coding is preferred.

Qualifications

• Experience with MedDRA and WHO Drug dictionaries for coding
• Strong understanding of clinical trial data workflows and coding conventions
• Ability to review and confirm adverse event coding with study stakeholders

Responsibilities

• Perform medical coding using MedDRA and WHO Drug dictionaries for post-marketing and in-house trials
• Coordinate with SABR staff and vendors to ensure coding is timely and accurate
• Conduct quality control/assurance activities for coding across studies

Skills

Clinical trial experience

Data management experience

Safety experience

Coding safety cases

Education

Nursing/Pharmacy degree

Job description

Integrated Resources, Inc is seeking a Medical Coder in Cambridge, MA to conduct centralized coding activities using MedDRA and WHO Drug dictionaries, supporting clinical trials and pharmacovigilance.

You will work with the Study Management Team, CDPM and CP to align coding targets with study timelines, review adverse event coding with SABR physicians, and ensure accuracy across in-house and outsourced trials. Experience in data management or safety coding is preferred.