Join Bristol Myers Squibb in Hyderabad as a Clinical Trial Risk Analyst!
Summary: Bristol Myers Squibb (BMS), a leading global pharmaceutical company, is seeking talented and experienced individuals to join our team in Hyderabad, India. We are currently hiring for both Manager and Senior Manager roles within our Clinical Trial Risk Analyst department. These positions are crucial to supporting our Risk-Based Monitoring (RBM) strategy, ensuring the highest standards of data quality, patient safety, and protocol compliance across our global clinical trial operations. If you possess a strong background in clinical research, RBM analytics, GCP, data visualization, and risk governance, we encourage you to apply and contribute to our mission of discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases.
Role 1: Manager – Clinical Trial Risk Analyst
Location: Hyderabad, India
Department: Trial Delivery Support (TRIM)
About the Role:
As a Manager – Clinical Trial Risk Analyst, you will play a vital role in ensuring the quality and integrity of our clinical trials through effective risk assessment and analytics. You will work closely with study teams to develop and implement risk-based monitoring strategies, identify potential issues, and contribute to a robust risk governance framework.
Key Responsibilities:
- Lead and execute clinical risk assessments and analytics for assigned clinical trials.
- Collaborate with study teams to develop Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and comprehensive data review plans.
- Conduct centralized monitoring activities to identify trends, outliers, and potential data quality signals.
- Generate study-level risk reports to provide actionable insights to relevant stakeholders.
- Proactively identify and escalate potential quality or compliance issues, contributing to the overall risk governance process.
- Contribute to the development and improvement of RBM processes and strategies.
Required Qualifications:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Data Science, Analytics, or a related field.
- Minimum of 3 years of experience in clinical operations or the pharmaceutical industry.
- Strong understanding of Risk-Based Monitoring (RBM) principles and methodologies.
- Familiarity with Risk Assessment and Categorization Tool (RACT) and Good Clinical Practice (GCP) guidelines.
- Proficiency in data platforms such as Veeva and data visualization tools.
- Ability to interpret complex data sets and effectively communicate findings and insights.
- Experience with audits, Corrective and Preventive Actions (CAPA), and regulatory expectations is preferred.
- Excellent analytical, problem-solving, and communication skills.
Estimated Salary: ₹18 – 30 LPA (approx.)
Role 2: Senior Manager – Clinical Trial Risk Analyst (Line Manager)
Location: Hyderabad, India
Department: TRIM Leadership
About the Role:
As a Senior Manager – Clinical Trial Risk Analyst, you will lead a team of talented risk analysts, driving the implementation of Risk-Based Monitoring initiatives and ensuring the effective oversight of clinical trial risks. You will be responsible for the professional development of your team and contribute to the strategic direction of the TRIM department.
Key Responsibilities:
- Lead, mentor, and manage a team of Clinical Trial Risk Analysts, fostering a collaborative and high-performing environment.
- Drive the implementation of Risk-Based Monitoring initiatives across assigned clinical trials and programs.
- Allocate project resources effectively, optimize workload planning, and ensure timely delivery of results.
- Provide coaching, performance reviews, and talent development opportunities for team members.
- Oversee the identification, assessment, and mitigation of clinical trial risks.
- Support escalations to governance committees and senior leadership, providing clear and concise risk narratives.
- Contribute to the development and refinement of RBM strategies and best practices.
Required Qualifications:
- Strong expertise in Risk-Based Monitoring (RBM) strategy, Good Clinical Practice (GCP) guidelines, clinical analytics, and data modeling.
- Proven experience in people leadership, team management, and stakeholder engagement.
- Excellent ability to present complex data as compelling risk narratives for diverse audiences.
- Exposure to health authority audits and Corrective and Preventive Actions (CAPA) processes is preferred.
- Advanced analytical, problem-solving, and decision-making skills.
- Excellent communication, interpersonal, and leadership skills.
Estimated Salary: ₹28 – 45 LPA (approx.)
Benefits of Working at BMS
At Bristol Myers Squibb, we are committed to creating a rewarding and fulfilling work environment for our employees. We offer:
- Competitive compensation and performance-based rewards.
- A flexible work environment that supports work-life balance.
- Opportunities for global exposure and cross-functional collaboration.
- Extensive career growth and development opportunities, including advanced industry training.
- A culture of innovation, collaboration, and respect.
Ready to Apply?
If you are a motivated and experienced professional looking to make a significant impact in the pharmaceutical industry, we encourage you to apply!
To Apply:
Please visit the Bristol Myers Squibb careers website and search for the following job postings:
- Manager – Clinical Trial Risk Analyst: Search for requisition number [Insert Requisition Number Here – Find the real one on the site]
- Senior Manager – Clinical Trial Risk Analyst: Search for requisition number [Insert Requisition Number Here – Find the real one on the site]
We look forward to receiving your application!
Bristol Myers Squibb is an equal opportunity employer committed to diversity and inclusion. We encourage applications from all qualified individuals.