Job Title: Manager, Clinical Data Reporting & Analytics
Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb (BMS)
Job Type: Full-Time, Regular
Job Summary:
The Manager, Clinical Data Reporting & Analytics will serve as the primary point of contact for multiple clinical studies across different Therapeutic Areas. The role involves collaborating with stakeholders to develop and implement reporting solutions aligned with study protocols, ensuring compliance, and supporting clinical trial operations. This role is critical in analyzing clinical data, developing reports, and ensuring patient safety through effective monitoring approaches.
Key Responsibilities:
1. Clinical Data Reporting & Analytics
Act as the primary point of contact for multiple clinical studies across therapeutic areas.
Collaborate with clinical stakeholders to understand reporting and analytics needs.
Develop reports and analytics visualizations according to specifications while ensuring a "first-time right" approach.
Utilize standard reports whenever possible and suggest solutions where necessary.
Test developed reports, document results, and provide peer review support.
2. Compliance & Documentation
Ensure adherence to documentation and compliance processes.
Notify management of any process deviations and noncompliance issues.
Maintain accurate and up-to-date records for audit readiness.
3. Clinical Trial Monitoring & Stakeholder Management
Analyze clinical trial needs holistically to determine effective monitoring approaches.
Prioritize deliverables based on business criticality and negotiate with stakeholders to ensure timely report delivery.
Work collaboratively with internal and external stakeholders, including Clinical Operations, Biostatistics, and Regulatory Affairs teams.
4. Continuous Improvement & Technical Expertise
Stay updated with the latest reporting tools, industry trends, and regulatory guidelines.
Contribute to process improvements and best practices for clinical data analytics.
Support other sub-functions within Clinical Data Reporting & Analytics (CDR&A) as needed.
Required Qualifications & Experience:
Education & Experience:
Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Pharmacy, Statistics, Data Science, or a related field.
5+ years of experience in clinical data reporting, analytics, or related roles within the pharmaceutical, biotechnology, or CRO industry.
Experience with clinical trial data management systems, reporting tools, and visualization software.
Technical Skills:
Expertise in clinical data management tools (e.g., Medidata, Oracle Clinical, SAS, R, Python).
Proficiency in data visualization tools (Tableau, Spotfire, Power BI).
Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
Experience in SQL, relational databases, and clinical data standards (CDISC, SDTM, ADaM) is a plus.
Soft Skills:
Excellent communication, stakeholder management, and problem-solving skills.
Ability to work in a fast-paced, cross-functional global environment.
Strong analytical and critical thinking abilities for clinical data interpretation.
Work Environment & Location:
Location: Hyderabad, Telangana, India.
Work Model: Hybrid (Minimum 50% on-site presence required).
Flexibility to collaborate with global stakeholders across different time zones.
Diversity & Inclusion Statement:
BMS is committed to diversity and equal employment opportunities. We encourage candidates from all backgrounds to apply. Reasonable accommodations are available for candidates requiring assistance in the recruitment process.
For more information, visit careers.bms.com.
Application Process:
Interested candidates can apply through the BMS Careers Portal or via LinkedIn.
Note: If you don’t meet every requirement but are passionate about clinical data analytics, we encourage you to apply!
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