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Manager, Clinical Trial Risk Analyst

3 years
Not Disclosed
10 Nov. 20, 2025
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager, Clinical Trial Risk Analyst

Location: Hyderabad, Telangana, India
Category: Clinical Trial Operations & Risk Management

Position Overview

The Manager, Clinical Trial Risk Analyst plays a key role within the Trial Delivery Support (TDS) and Trial Risk & Integrity Management (TRIM) function. This position supports the Risk-Based Management (RBM) framework by providing comprehensive study-level risk analysis, data quality oversight, and risk monitoring for clinical trials within Bristol Myers Squibb’s global portfolio.

The role focuses on remote risk identification, data analytics, trend detection, and proactive risk mitigation to ensure compliance, patient safety, and high-quality clinical data. The position works cross-functionally with statistical, clinical, data management, quality, and operational teams to guide risk strategies across multiple studies.


Key Responsibilities

Risk Assessment & Protocol De-Risking

  • Support protocol de-risking by identifying critical-to-quality factors, critical data elements, and key processes essential for study success.

  • Collaborate with study leadership, statisticians, and medical teams to define Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and data review strategies.

  • Develop specifications for KRIs, Data Quality Assessments (DQA), and QTL frameworks.

Risk Monitoring & Data Analytics

  • Conduct regular study-level risk monitoring using advanced statistical and data visualization methodologies.

  • Review aggregated clinical and operational data to identify trends, outliers, and emerging risks.

  • Prepare holistic risk reports, facilitate escalation of significant risks, and support governance discussions.

  • Triages risk signals for Risk Review Meetings and recommends appropriate follow-up actions.

Cross-Functional Collaboration

  • Work closely with Data Management, Clinical Operations, Quality, Medical, and Therapeutic Area teams to ensure unified risk oversight.

  • Contribute to continuous risk discussions throughout the trial lifecycle and ensure updates to risk management plans.

  • Provide insights linking risk signals to root causes and actionable mitigation strategies.

Quality Oversight & Compliance

  • Ensure adherence to GCP, regulatory guidance, and BMS RBM standards.

  • Support audits, inspections, and internal quality reviews by preparing risk documentation and analytics.

  • Guide external partners including CROs and service providers performing risk management activities.

Continuous Improvement & Innovation

  • Participate in process optimization initiatives within TRIM and the broader organization.

  • Contribute to the development of RBM-related tools, dashboards, and visualization models.

  • Support capability building and training programs focused on risk-based monitoring and data-driven oversight.


Qualifications (Minimum Required)

  • Bachelor’s degree in Life Sciences, Data Science, Statistics, Analytics, Business, or related fields.

  • Minimum 3 years of experience in the pharmaceutical or biotech industry with exposure to drug development.

  • Minimum 3 years of experience in clinical trial operations, GCP compliance, or risk-based monitoring.

  • Strong understanding of risk-based monitoring principles including Quality by Design, risk assessment, and risk control methodologies.

  • Proficiency in data analysis, data interpretation, and visualization with the ability to communicate insights clearly.

  • Working knowledge of regulatory expectations, GCP, and global compliance standards.

  • Experience working with tools such as RACT, RBM analytics platforms, Veeva systems, or equivalent.


Preferred Qualifications

  • Experience in audits, inspections, CAPA processes, and root cause analysis.

  • Strong interpersonal, collaboration, and stakeholder management skills.

  • Ability to build compelling data-driven narratives tailored to diverse audiences.

  • Demonstrated capability to align operational priorities with organizational goals.

  • Adaptability, proactive problem-solving skills, and willingness to innovate within evolving environments.


Experience Required (Summary)

  • 3+ years in pharmaceutical/biotech clinical trial operations.

  • 3+ years of experience with GCP, RBM, or clinical study oversight.

  • Strong background in data analytics, risk assessment, and clinical data interpretation.


Work Model

BMS follows an occupancy structure aligned with operational needs:

  • Roles may be site-essential, site-by-design (hybrid), remote-by-design, or field-based.

  • Onsite presence or travel may be required depending on responsibilities and business needs.