Mgr Clinical Risk Management

Amgen

Hyderabad, India
Fully remote
Risk-based quality management (rbqm)
Centralized monitoring
Key risk indicators (kris)
The Clinical Risk Analyst is responsible for generating and translating study-level risk insights to enable proactive, data-driven decision-making across the conduct of clinical trials

Job Summary

  • The Clinical Risk Analyst is responsible for generating and translating study-level risk insights to enable proactive, data-driven decision-making across the conduct of clinical trials.
  • This role is a key driver of Risk-Based Quality Management (RBQM), leveraging centralized monitoring, analytics, and cross-functional data sources to identify, assess, and mitigate risks to patient safety, data integrity, and study delivery.
  • Lead centralized monitoring reviews using platforms such as CluePoints to drive risk identification, signal detection, trend analysis, and structured decision-making across assigned studies.

Matching Summary

The Clinical Risk Analyst is responsible for generating and translating study-level risk insights to enable proactive, data-driven decision-making across the conduct of clinical trials.

Skills & Requirements

Must-have

  • Risk-Based Quality Management (RBQM)
  • centralized monitoring
  • Key Risk Indicators (KRIs)
  • Quality Tolerance Limits (QTLs)
  • Root Cause Analysis (RCA)
  • CluePoints platform

Nice-to-have

  • strategic thinking and problem-solving
  • cross-functional data sources
  • continuous improvement
  • collaboration across global teams

Key Requirements

  • Doctorate degree and 1 year of clinical operations execution experience
  • Master’s degree and 2 years of clinical operations execution experience
  • Bachelor’s degree and 4 years of clinical operations execution experience
  • Associate’s degree and 8 years of clinical operations execution experience
  • High school diploma / GED and 10 years of clinical operations execution experience
  • 5 years work experience in life sciences or medically related field
  • 3 years of biopharmaceutical clinical research experience
  • Experience working in global clinical trial teams
  • Experience with risk-based site monitoring
  • Experience with data-driven oversight in Risk Based Quality Management (RBQM) approaches

Work Rights

Not specified

Tailored Resume

Cover Letter