India's DMPLOI - Jobs & Networking AppAmgen, a global biotechnology leader, is hiring for the position of Central Monitor Senior Associate at its Hyderabad location. This is an excellent opportunity for clinical research professionals with experience in centralized monitoring, risk-based quality management, and clinical trial analytics to join one of the world’s leading biopharmaceutical companies.
About Amgen
Founded in 1980, Amgen is dedicated to serving patients living with serious illnesses through innovative biotechnology solutions. The company focuses on key therapeutic areas including Oncology, Inflammation, General Medicine, and Rare Diseases, helping millions of patients worldwide.
Amgen’s collaborative and science-driven culture provides employees with opportunities to make a meaningful impact while advancing their careers.
Job Details
| Particulars | Details |
|---|---|
| Position | Central Monitor Senior Associate |
| Company | Amgen |
| Job ID | R-247074 |
| Location | Hyderabad, India |
| Work Type | On-Site |
| Experience Required | 4+ Years |
| Qualification | Graduate / Postgraduate |
| Industry | Clinical Research / Life Sciences |
Key Responsibilities
As a Central Monitor Senior Associate, you will play a critical role in supporting clinical trial quality and patient safety through proactive, data-driven monitoring activities.
Major Responsibilities Include:
- Execute proactive risk surveillance using central monitoring analytics.
- Identify trends, anomalies, and emerging risks across assigned studies and sites.
- Perform independent signal detection, triage, and prioritization of risks.
- Translate statistical and operational findings into actionable insights.
- Support Risk-Based Quality Management (RBQM) strategies, including:
- Site Risk Assessments (SRAs)
- Key Risk Indicators (KRIs)
- Quality Tolerance Limits (QTLs)
- Conduct study-level and site-level analytics reviews.
- Collaborate with study teams to implement corrective and preventive actions.
- Maintain inspection-ready documentation aligned with regulatory requirements.
- Engage with Clinical Research Associates (CRAs) and cross-functional stakeholders.
- Mentor and guide junior central monitoring team members.
Eligibility Criteria
Basic Qualification
- Graduate or Postgraduate degree.
- Minimum 4 years of experience in Central Monitoring.
Preferred Qualifications
Candidates with the following experience will be preferred:
- 4–8 years of experience in Life Sciences or related medical fields.
- Experience in centralized monitoring and centralized review activities.
- Knowledge of Risk-Based Monitoring (RBM) and Risk-Based Quality Management (RBQM).
- Experience working on global clinical trials across multiple geographies.
- Strong analytical skills with the ability to identify trends in clinical trial datasets.
- Experience using central monitoring tools and methodologies.
- Ability to create high-quality, inspection-ready documentation.
- Mentoring and coaching experience for junior team members.
Why Join Amgen?
Amgen offers employees an opportunity to contribute to life-changing therapies while enjoying a supportive and innovative work environment.
Benefits of Working at Amgen
- Global career growth opportunities
- Collaborative and science-driven culture
- Competitive compensation and benefits
- Exposure to international clinical trials
- Professional development and learning programs
- Opportunity to work on innovative therapies impacting millions of patients
How to Apply
Interested and eligible candidates can apply online through the official Amgen careers portal by searching for:
Job Title: Central Monitor Senior Associate
Job ID: R-247074
Location: Hyderabad, India
Apply soon and become part of Amgen’s mission to transform the lives of patients worldwide through innovation and science.
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