57 matching jobs for “Study Delivery Associate”

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Amgen

Associate Director, Biostatistical Programming

Hyderabad, India

Full time
Regular

Associate Director, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of …

Added Oct 15, 2026

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Amgen

Associate Director, Biostatistical Programming

Hyderabad, India

Full time
Regular

Associate Director, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Hyderabad, India

Full time
Regular

Job Description Biostatistical Programming Senior Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Hyderabad, India 3 postings

Full time
Regular

Biostatistical Programming Senior Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Hyderabad, India

Full time
Regular

Biostatistical Programming Senior Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Hyderabad, India

Full time
Regular

Biostatistical Programming Senior Associate HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Hyderabad, India

Full time
Regular

… patients worldwide. It’s time for a career you can be proud of. Join us. Biostatistical Programming Senior Associate What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Statistical …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate

Taipei, Taiwan

Full time
Regular

… (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Biostatistical Programming Senior Associate in Taipei, Taiwan. Live What you will do Amgen is expanding its global Statistical Programming …

Added Oct 15, 2026

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Amgen

Biostatistics Sr Associate – Data Visualization

Hyderabad, India

Full time
Regular

… over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Biostatistics Sr Associate What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics …

Added Oct 15, 2026

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Amgen

Data Management Sr Associate

Hyderabad, India

Full time
Regular

… Support What you will do Let’s do this. Let’s change the world. In this vital role you will support the delivery of high-quality clinical trial data by executing core data management activities across the study …

Added Oct 15, 2026

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Amgen

Associate Director - Information Systems

US - California - Thousand Oaks

Full time
Regular

… as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Director - Information Systems - Clinical Data Hub What you will do Let’s do this. Let’s change the world. …

Added Oct 15, 2026

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Amgen

Database Design Sr Associate

Hyderabad, India

Full time
Regular

… known today. ABOUT THE ROLE Role Description: The Senior Database Designer is responsible for translating study protocol requirements into compliant, scalable, and efficient database configurations within Vault CDMS, …

Added Oct 15, 2026

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Amgen

Senior Associate Safety Data Analyst

Hyderabad, India

Full time
Regular

… safety system Key Activities: With limited direction from Sr. Manager-Safety Data Analyst (SDA), the Sr. Associate - SDA may perform the following activities: Generate outputs from the global safety system in support of …

Added Oct 15, 2026

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Amgen

Seniorr Associate Regulatory Writing

Hyderabad, India

Full time
Regular

… by providing documentation history and rationale when needed. Engage with Clinical, Safety, Regulatory and Study teams to clarify inputs, resolve comments and incorporate feedback efficiently Participate in document …

Added Oct 15, 2026

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Amgen

Associate Director, Development Analytical Reporting

Hyderabad, India

Full time
Regular

Associate Director, Analytical Reporting Department Name: Global Development Operations - Data Management Role GCF: …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate (Innovation)

Hyderabad, India

Full time
Regular

Biostatistical Programming Senior Associate ( Innovation) HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s …

Added Oct 15, 2026

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Amgen

Sr. Associate Regulatory Affairs

Hyderabad, India

Full time
Regular

… renewals, and product renewals Interact with authors/reviewers and subject matter experts with respect to delivery of CMC and/or Device documents required for regulatory submissions Preparing submission content plans for …

Added Oct 15, 2026

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Amgen

Senior Associate - Strategic Planning & Operations

Hyderabad, India

Full time
Regular

… to the design of clinical trials and the safety and efficacy of Amgen medicines. We are seeking a Senior Associate, Strategic Planning & Operations , to join the Center for Observational Research (CfOR). This role will …

Added Oct 15, 2026

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Amgen

Biostatistical Programming Senior Associate (POPPK/PD)

Hyderabad, India

Full time
Regular

Biostatistical Programming Senior Associate ( POPPK/PD) HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because …

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Amgen

Global Regulatory Writing – Senior Associate

Hyderabad, India

Full time
Regular

… documentation, and justification/rationale as required. Collaborate with Clinical, Safety, Regulatory, and Study teams to clarify inputs, resolve comments, and efficiently incorporate feedback. Participate in …

Added Oct 15, 2026

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Amgen

Associate Director, Biostatistical Programming

Hyderabad, India

Full time
Regular

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Basic Qualifications · employer excerpt

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 16 years of statistical programming experience in clinical development environment.
Strong technical, communication, and leadership skills
Ability to lead and manage a large team of programmers in successful and timely completion of all programming activities for highly complex studies and regulatory submissions
Experience developing a successful offshore statistical programming team
Flexibility and desire to work across different time-zones

7 more in the full description below.

About this opportunity

Original employer description

Career Category

Clinical

Job Description

Associate Director, Biostatistical Programming

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

Associate Director, Biostatistical Programming

What you will do

Let’s do this. Let’s change the world.

Amgen is expanding its Global Statistical Programming (GSP) capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As an Associate Director of Biostatistical Programming (Programming Execution Lead), you will partner with Global Programming Leads (GPL) and lead a large offshore team of Study Lead Programmers (SLP) and Study Programmers (SP) to successfully execute end-to-end programming activities for all studies and global regulatory approval submissions for large, high priority products or indications across products. Together with GPL, this Associate Director will be accountable and responsible for Global Statistical Programming study results and submission activities for the assigned products or indications across products.

The Associate Director of Biostatistical Programming will contribute at the department level by leading major GSP technical or operational efficiency initiatives and ensuring compliance with R&D standards, leading or serving as a member of GSP and cross functional consultancy groups such as Submission Consultancy Group and ADaM Consultancy Group.

The Associate Director will drive the piloting and integration of new technologies, including artificial intelligence, statistical programming automation tools, and open-source platforms to improve quality and efficiency across the organization.

Key Responsibilities:

Accountable and responsible for ensuring successful execution and delivery of GSP milestone analysis deliverables and regulatory submission packages for a group of high priority and/or high complexity Amgen products being supported by the offshore programming team.
Work with GPL to ensure successful implementation of programming strategies such as functional standards and industry requirements for the assigned products globally.
Plan and monitor progress of projects and address issues accordingly.
Provide GSP product level input to developing and managing resource plans and budgets for GSP.
Efficiently and effectively monitor and utilize assigned staff at product level according to priorities.
Drive the piloting and integration of new technologies, including artificial intelligence, statistical automation tools, and open-source platforms to improve functional maturity and efficiency.
Lead and/or participate in departmental process improvement initiatives and cross-functional working groups.
Represent GSP in study and system audits and inspections by internal and external bodies.
Develop, review, and implement Policies, SOPs and other controlled documents affecting GSP globally.
Provide hands-on support to the assigned product areas as required.
Provide coaching and mentoring to GSP staff globally.
Provide input into career development plans to direct reports and staff on assigned projects

This position will be located at Amgen India (Hyderabad).

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a results-oriented, tech-forward programming leader with deep expertise in clinical trial operations and digital transformation.

Basic Qualifications:

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 16 years of statistical programming experience in clinical development environment.
Strong technical, communication, and leadership skills
Ability to lead and manage a large team of programmers in successful and timely completion of all programming activities for highly complex studies and regulatory submissions
Experience developing a successful offshore statistical programming team
Flexibility and desire to work across different time-zones
Advanced analysis and reporting skills in SAS (including SAS/STAT, Macro, Graph, SQL, and others) or R
Prior regulatory submission experience for approval
Thorough understanding and experience with data quality and compliance checks
Experience working effectively in a globally dispersed team environment with cross-cultural partners
Prior staff development leadership and project management experience
Excellent oral and written English communication skills
Ability to effectively perform complex statistical programming and related tasks

Preferred Skills:

MSc or higher degree in statistics, biostatistics, mathematics, or related quantitative or scientific subjects
Familiarity with open-source programming tools (e.g., R, Python), automation platforms, and emerging technologies in statistical programming

Why this result? · Employer labels

Keywords also found in description

Clinical
Full time
Regular

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