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. 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 .
The Associate Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.

Position Summary

• Supports execution of assigned clinical trial activities and works closely with Clinical Scientist to execute activities associated with trial conduct
• Supports trial level activities for one or more trials with the necessary supervision

Position Responsibilities

• Seek out and enact best practices with instruction
• Provide regular and timely updates to manager/management as requested
• Support development of Protocol and ICF documents/amendments
• Conduct literature review. Support submission of clinical documents to TMF
• Support development of site and CRA training materials
• Review clinical narratives
• Collaborate cross-functionally to monitor clinical data for specific trends
• Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming

Degree Requirements

• Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field preferred)
• Appropriate for new entrance to pharma

Experience Requirements

• Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations

Key Competency Requirements

• Detail-oriented with commitment to quality
• Critical thinking and problem-solving skills
• Adaptable/flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)
• Proficient skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)

Travel Required (nature and frequency)

• Domestic and International travel may be required

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.

• Seek out and enact best practices with instruction
• Provide regular and timely updates to manager/management as requested
• Support development of Protocol and ICF documents/amendments
• Conduct literature review. Support submission of clinical documents to TMF
• Support development of site and CRA training materials
• Review clinical narratives
• Collaborate cross-functionally to monitor clinical data for specific trends
• Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programmin