Central Monitor

Amgen SA; Hyderabad; On-site; INR 1,500,000 - 2,500,000; Full time

Job summary

Amgen SA in Hyderabad is seeking a Central Monitor to lead data-driven risk surveillance across studies using analytics to identify trends and emerging risks. The ideal candidate will have a Doctorate/Master’s degree and 8-15 years of clinical execution experience, preferably with a strong background in biopharmaceutical clinical research and risk-based quality management. This role offers a collaborative culture focused on professional growth and well-being.

Qualifications

• 8-15 years of clinical execution experience.
• Minimum 8 years in life sciences or related field.
• Experience in clinical research data management.

Responsibilities

• Lead proactive risk surveillance with analytics.
• Translate findings into actionable insights.
• Document outputs and align with regulatory standards.

Skills

Data-driven risk surveillance

Statistical analysis

Signal detection

Risk-based monitoring

Clinical trial management

Education

Doctorate/Master’s degree

Job description

Central Monitor

What you will do

• Lead proactive, data-driven risk surveillance across studies using central monitoring analytics to detect trends, anomalies, and emerging risks
• Translate complex statistical and operational findings into clear, actionable insights, recommending targeted interventions to study teams, CRAs, and functional leads
• Partner closely with Data Delivery Leads to implement, monitor, and continuously refine RBQM strategies (e.g., QTLs, KRIs, SRAs) across the study lifecycle
• Act as a subject matter expert in central monitoring tools and methodologies, driving consistent use and elevating team capability in signal detection and interpretation
• Document signal detection outputs, rationale, and recommended actions in an inspection‑ready manner aligned with regulatory and internal governance expectations
• Facilitate feedback loops across sites, CRAs, and study teams to ensure issues are resolved and drive continuous process and quality improvement across the portfolio

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Basic Qualifications

• Doctorate/Master’s degree with 8-15 years of clinical execution experience

Preferred Qualifications

• Minimum 8 years of work experience in life sciences or medically related field, including 3+ years of managing data on biopharmaceutical clinical research experience
• Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
• Experience with risk-based monitoring models / risk-based quality management, and/or clinical site management
• Experience in analyzing broad clinical trial data sets for trends

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well‑being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.