Senior Manager, Development Analytical Reporting

Amgen Inc. (IR); Hyderabad; On-site; INR 1,800,000 - 2,800,000; Full time

Job summary

Amgen Inc. in Hyderabad, India, is seeking an Associate Director to lead clinical analytical reporting and data-review technology across Global Development. You will guide multiple teams, set capability roadmaps, govern the reporting portfolio and influence enterprise data decisions.

The role blends strategic leadership with hands-on problem solving, ensuring quality, compliance and scalable analytics solutions, while partnering with Data Management, Biostatistics and Digital Technology.

Qualifications

• Doctorate degree with 5+ years of relevant experience or Master’s with 8+ years or Bachelor’s with 10+ years.
• 2+ years of people-management experience in clinical data, analytics or related environment.
• Experience delivering clinical data reports, dashboards and data-review solutions in regulated settings.

Responsibilities

• Provide strategic leadership for analytical reporting programs and data-review technology.
• Lead teams, set goals, governance and delivery priorities for study and program work.
• Drive adoption of reusable components and standardized data definitions across the portfolio.
• Ensure quality, compliance and lifecycle management for reporting solutions.

Skills

SQL

Python

SAS

R

Databricks

Power BI

Spotfire

Tableau

Education

Doctorate degree

Master's degree

Bachelor's degree

Tools

Job description

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Let’s do this. Let’s change the world.

In this vital role, you will provide strategic and organizational leadership for clinical analytical reporting, data-review technology and data-product capabilities across Global Development. Building on Sr. Manager accountability for a delivery team, you will lead multiple teams or workstreams, set the multi-year capability and technology roadmap, govern the reporting portfolio and influence enterprise data and digital decisions. You will remain technically credible while operating primarily through leaders, strategic partnerships and portfolio-level decisions.

What you will do

• People, delivery and technical leadership Lead, coach and develop a team of analytical reporting programmers and technical specialists; set clear goals, create development plans and build an inclusive, accountable and high-performing team culture. Own capacity planning, prioritization and delivery governance for the team’s study, program and capability work; balance urgent study needs with reusable, scalable solutions. Provide technical direction and review for clinical reports, dashboards, visualization standards, data transformations and advanced data-review solutions, remaining sufficiently hands-on to resolve complex issues and make sound technical decisions. Establish consistent intake, estimation, development, peer-review, testing, release and support practices across the team.
• Clinical analytical reporting and data products Ensure timely, high-quality delivery of patient profiles, listings, cross-domain reports, medical and safety review dashboards, operational metrics, data-quality indicators and other study- and program-level solutions. Oversee development of curated, analysis-ready clinical datasets that integrate approved EDC and external data and support traceable, repeatable reporting. Drive adoption of reusable components, standard templates, common data definitions and metadata-driven approaches that reduce duplication and improve consistency. Sponsor practical use of anomaly detection, advanced analytics and automation to surface data issues, trends and potential risks, with documented validation and appropriate human review.
• Cross-functional partnership and operational excellence Partner with leaders and SMEs in Data Management, Medical Data Review, Safety, Clinical Operations, Biostatistics, Therapeutic Areas, Clinical Systems and Digital Technology to define priorities and fit-for-purpose solutions. Represent Analytical Reporting in study and program governance; communicate delivery status, risks, trade-offs and decision recommendations clearly to stakeholders. Manage vendor or contingent-resource delivery within assigned scope, including quality oversight, performance feedback and acceptance of deliverables. Establish meaningful service, quality and adoption metrics; use findings to drive root-cause analysis, continuous improvement and transparent performance management.
• Quality, compliance and capability building Ensure reporting solutions comply with ICH-GCP, applicable regulations, Amgen policies, data-integrity expectations, privacy and security requirements, and controlled-system practices. Maintain inspection-ready evidence for development, validation, release and lifecycle management; support audits, inspections and corrective actions. Contribute to the analytical reporting roadmap, technology evaluation, SOPs, standards and communities of practice; identify emerging needs for the Associate Director.

What we expect of you

• Basic qualifications Doctorate degree and 5+ years of relevant experience; OR Master’s degree and 8+ years of relevant experience; OR Bachelor’s degree and 10+ years of relevant experience. 2+ years of people-management experience, or demonstrated leadership of a significant technical team or capability, in clinical development, data management, programming, analytics, data science or a related environment. Demonstrated experience delivering clinical data reports, dashboards, visualizations, analytical datasets or data-review solutions in pharmaceutical, biotechnology, CRO or closely related regulated settings.
• Preferred qualifications Experience leading teams that use SQL, Python, SAS, R, Databricks, Power BI, Spotfire, Tableau or comparable platforms. Strong understanding of clinical development and data-review workflows, EDC and external clinical data, CDISC standards, data governance and regulated-system validation. Experience building operating practices, capacity plans, quality metrics and vendor-management models in a global matrix environment. Experience evaluating AI, machine learning or intelligent automation in a regulated setting, including validation, traceability and human-oversight considerations. Strong stakeholder management, change leadership, communication and talent-development skills.

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen