Medical Coder

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

Medical Coder

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri‑states most well‑respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Position Details: Client Direct Client

Location Cambridge, MA

Job Title Medical Coder Position

Duration 9+ Months

Must have skill-set [Job Description]

Job Summary

The Medical Coder is responsible for conduct of centralized medical coding activities. As part of the study management team (SMT), the Medical Coder works in partnership with the Clinical Data Project Manager (CDPM) and Clinical Programmer (CP) to ensure coding targets are identified during database development and also partners with SABR MDs to review and approve clinical trial adverse event coding as needed according to study timelines and deliverables.

Principal Accountabilities

• Perform medical coding (WHO Drug Dictionary Enhanced and MedDRA) activities maintaining optimal communication with SABR staff and SABR vendors for all post marketing cases managed by SABR as per applicable coding conventions
• Perform medical coding activities for all in-house clinical trials maintaining optimal communication with internal DM staff and oversight of vendors performing coding for out-sourced (full service and FSP) clinical trials while maintaining optimal communication with vendor staff as per applicable coding conventions.
• Perform quality control and quality assurance activities for all medical coding activities, including in-house and outsourced coding activities. General Knowledge and Skills

General Knowledge and Skills

• Clinical trial experience, preferably data management and/or safety experience, preferably coding safety cases.

Qualifications

• 2-5 years medical coding using the MedDRA and WHO Drug dictionaries as well as the structure and function of systems used to perform coding Possesses a degree in nursing, pharmacy or other related medical field.

Additional Information

Thanks!!!

Warm Regards,

Amrit Singh

Clinical Recruiter Integrated Resources, Inc