Bristol Myers Squibb Hiring for Senior Manager, Medical Coding at Hyderabad, India Full Time

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.

Functional Area Description

GDM&CM is responsible for clinical trial data acquisition, data standards governance, data management, medical coding, data reporting and analytics, and centralized monitoring for trials across the BMS R&D portfolio.

Position Summary / Objective

Senior Manager, Medical Coding will be responsible for oversight of medical coding activities for assigned programs or projects or for assisting with the management of industry standard terminologies (MedDRA, UMC WHODrug), or company specific dictionaries and supporting synonym tables.

This role reports to the Director, Medical Coding or the Associate Director, Medical Coding within GDM&CM.

Position Responsibilities

• Responsible for delivering accurate and consistent medical coding for all assigned protocols within established timelines and in compliance with all processes, guidelines, and conventions.

• Interfaces with colleagues from study teams on coding related matters and serves as the medical coding subject matter expert.

• Oversight of the review and approval of coded terms in clinical trials designated for coding with MedDRA, UMC WHODrug, or company specific dictionary ensuring that coding is clear, appropriate, and complete based upon the investigator’s entry on the CRF and coded in compliance with all processes, guidelines and conventions.

• Perform periodic review of industry best practices and coordinate the review and updating of BMS guidelines to ensure alignment.

• Creating and maintaining company specific Standardized MedDRA Queries or Custom Drug Groupings partnership with medical, clinical, and other key functions.

• Perform ongoing review of the MedDRA, UMC WHODrug or company specific dictionary synonym tables to ensure coding is accurate, consistent and reflects the most appropriate dictionary term available in the current version of the dictionary.

• Establishes and maintains communications between safety, clinical and vendors to ensure MedDRA, UMC WHODrug or company specific dictionary coding is consistency between the safety system, clinical coding system and CRO systems.

• Support maintenance activities for coding tools, including script creation and execution to support User Acceptance Testing (UAT).

• Creating and maintaining company specific Standardized MedDRA Queries or Custom Drug Groupings partnership with medical, clinical, and other key functions.

• Provide ad hoc medical coding expertise in support of regulatory activities (e.g., periodic safety updates, submissions, etc.).

• Ensure effective quality oversight and management of external partners (e.g., Functional Service Providers, CROs, etc.) performing medical coding services on behalf of BMS.

• Knowledge of general clinical research and of the pharmaceutical industry. Thorough understanding of Regulations, GCP, ICH Guidelines as they apply to coding of medical terminology.

Degree Requirements

Bachelor’s Degree in the Life Sciences or R.N.

Experience Requirements

Minimum of 5-7 years coding in clinical research at a pharmaceutical or biotechnology company. Clinical data management experience is a plus. Working knowledge of Oracle Clinical TMS, Medidata Rave Coder.

Key Competency Requirements

• Experience with hierarchical dictionary reporting dictionaries; MedDRA and UMC WHODrug.

• Thorough understanding of the versioning of MedDRA and UMC WHODrug.

• Complete understanding of the construction, versioning, and maintenance of MedDRA

• Understanding of medical concepts, biology, and chemistry in support of medical coding

• Thorough understanding of regulations, GCP, ICH Guidelines as they apply to coding of medical terminology.

Travel Required

Periodic travel may be required.

#HYDDD #LI-Hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Company: Bristol-Myers Squibb

Req Number: R1579017

Updated: 2024-03-15 00:48:48.196 UTC

Location: Hyderabad,India

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.