Development Analytical Reporting Lead

Amgen Inc. (IR); Hyderabad; On-site; INR 2,500,000 - 5,000,000; Full time

Job summary

Amgen in Hyderabad seeks an Analytical Reporting Programming Lead to provide strategic and organizational leadership for clinical analytical reporting, data-review technology and data-product capabilities across Global Development.

You will lead multiple teams, shape the capability roadmap, govern the reporting portfolio and partner with Medical Data Review, Biostatistics and Digital Technology to deliver trusted, analysis-ready datasets.

Qualifications

• Bachelor’s degree plus 10+ years of relevant experience or advanced degrees with substantial clinical reporting experience.

Responsibilities

• Lead end-to-end design, development and support of complex reports, dashboards and data-review tools.
• Define technical approaches, solution architectures, data flows and testing strategies for analytics initiatives.
• Mentor associate and senior programmers through design reviews, code reviews and coaching.
• Establish data quality controls, governance, and scoping for reporting solutions.

Skills

SQL

Programming languages (Python, SAS, or

Enterprise visualization platforms

Statistical methods

Machine learning concepts

Education

Bachelor’s degree in life sciences, computer science, data science, statistics, bioinformatics, health informatics, engineering or a related discipline

Master’s degree

Doctorate degree

Tools

SAS

SQL

Python

R

Databricks

Power BI

Spotfire

Tableau

Job description

Career Category Clinical Development Job Description Analytical Reporting Programming Lead Department Name: Global Development Operations - Data Management Role GCF: 5

ABOUT AMGEN 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.

What you will do

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.

Technical leadership and solution delivery

Lead end-to-end design, development and support of complex patient-, study-, program- and portfolio-level reports, dashboards, visualizations and advanced data-review tools. Define technical approaches, solution architectures, data flows, reusable components, development standards and testing strategies for assigned initiatives. Lead curation, integration and transformation of EDC and approved external clinical data into trusted, analysis-ready datasets with clear lineage, quality controls and fit-for-purpose semantic definitions. Develop and evaluate anomaly-detection, pattern-recognition, automation and advanced analytical approaches; ensure outputs are interpretable, validated and appropriately reviewed by subject-matter experts. Provide hands-on expertise with approved languages, platforms and visualization tools, such as SAS, SQL, Python, R, Databricks, Power BI, Spotfire and Tableau, selecting technology based on business need and governed architecture.

Delivery leadership and stakeholder partnership

Translate complex review needs from Data Management, Medical Data Review, Safety, Clinical Operations, Biostatistics, Clinical Systems and Digital Technology into clear requirements, solution designs and prioritized delivery plans. Act as technical lead for defined studies, programs or capability initiatives; manage dependencies, risks, estimates and delivery milestones and communicate status to stakeholders. Mentor associate and senior programmers through design reviews, code reviews, troubleshooting and technical coaching; raise team capability without direct people-management accountability. Lead vendor or external-resource technical activities when assigned, including work review, UAT coordination and acceptance of deliverables.

Quality, governance and innovation

Establish and apply risk-based quality controls for data preparation, programming, visual design, testing, release and maintenance; ensure traceability and inspection readiness. Contribute to standards, SOPs, work instructions, reusable assets and governance forums for analytical reporting and clinical data review. Partner with architecture and platform teams to improve scalability, performance, privacy, security, access controls and controlled deployment of reporting solutions. Identify and pilot high-value improvements in automation, AI-enabled analytics and visualization; recommend scale-up only when value, validation and governance criteria are met.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The collaborative, technically credible and patient-focused professional we seek has the following qualifications.

Basic qualifications

Basic qualifications Bachelor’s degree in life sciences, computer science, data science, statistics, bioinformatics, health informatics, engineering or a related discipline and 10+ years of relevant experience; OR Master’s degree and 8+ years of relevant experience; OR Doctorate degree and 5+ years of relevant experience. Demonstrated experience designing and delivering clinical reports, dashboards, visualizations, analytical datasets or data-review solutions in pharmaceutical, biotechnology, CRO or closely related regulated settings.

Preferred qualifications

Advanced proficiency in SQL and at least one programming language such as Python, SAS or R, plus practical experience with one or more enterprise visualization platforms. Experience with clinical data models, EDC and external clinical data, CDISC standards, data lineage, metadata-driven development and regulated-system validation. Experience applying statistical, anomaly-detection, machine-learning or automation methods to clinical data with appropriate validation and human oversight. Demonstrated technical leadership across cross-functional initiatives, including design authority, mentoring and management of complex delivery risks.

EQUAL OPPORTUNITY STATEMENT

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