Clinical Trial Physician Rheumatology
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Job Location:
London Borough - UK
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials and manages Phase 1 Phase 3 studies with demonstrated decision making capabilities. It has matrix management responsibilities across the internal and external network and the role provides medical and scientific expertise to cross-functional BMS colleagues.
Position responsibilities
Medical Monitoring:
Team Leadership & Collaboration Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT) partnering with Clinical Scientists to provide medical oversight on protocol development including inclusion/exclusion criteria and safety considerations
Medical Monitoring & Safety Lead medical and eligibility data reviews assess safety-related serious adverse events in partnership with Worldwide Patient Safety and oversee site interactions and safety narratives
GCP & Compliance Uphold all GCP obligations for clinical conduct safety management guidelines and maintain up-to-date required training
Clinical Development Expertise & Strategy:
Clinical Strategy & Protocol Design Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols with a strategic focus on drug/asset knowledge disease area science and regulatory targets
Medical Oversight & Accountability Provide medical accountability across a group of studies leading benefit/risk analyses within a matrix team environment alongside Clinical Scientists
Study Execution & Delivery Partner with Clinical Scientists to support all aspects of study delivery including site activation enrollment and adjudication of protocol violations and deviations
Stakeholder Engagement & Thought Leadership Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science biomarker research and clinical program design
Scientific Expertise & Education Maintain deep up-to-date knowledge of the disease area through conference attendance and literature review while staying informed on the competitive landscape and providing ongoing protocol-specific medical education to study teams and investigators
Health Authority Interactions & Publications:
Health Authority & Advisory Engagement Serve as the medical point of expertise in key Health Authority interactions and advisory board meetings
Regulatory Writing & Submissions Author and draft clinical content for CSRs regulatory reports briefing books and submission documents including clinical narratives in partnership with Clinical Scientists
Qualifications and experience
- MD required (or equivalent)
- 5 or more years of Industry experience and/or clinical trials experience is required
- Ability to communicate information clearly and lead presentations in scientific and clinical settings
- Subspecialty training in applicable therapeutic area desired
- Expertise in the scientific method to test hypotheses including statistical design analysis and interpretation
- Expertise in drug development process
- Expertise in the components needed to execute an effective clinical plan and protocols
- Strong leadership skills with proven ability to lead and work effectively in a team environment
Domestic and International travel may be required.
#LI-Hybrid
If you come across a role that intrigues you but doesnt 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 a supportive culture promoting global participation 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 an 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.
Supporting People with Disabilities
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 . Visit to access our complete Equal Employment Opportunity statement.
Bristol Myers Squibb is Disability Confident Employer
A UK Government scheme
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.
Data Protection
We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R: Clinical Trial Physician - RheumatologyRequired Experience:
IC
Key Skills
- EMR Systems
- Post Residency Experience
- Occupational Health Experience
- Pain Management
- SOAP
- Primary Care Experience
- Medical Management
- Suturing
- Workers' Compensation Law
- Pharmacy Residency
- Botox Experience
- Epic
About Company
Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more
