Take Care Of Others
biotech
StudyDataDeliverMgr
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Study Data Deliver Mgr at Take Care Of Others. Skills: data management, clinical trial delivery, study conduct activities, data deliverables. management and oversight of data collected within a study/program. lead end-to-end data management”
What You'll Achieve.
high-quality, timely, and decision-ready data that enables successful clinical trial delivery; delivery ready at all times; on-time delivery; high-quality outputs
Industry & Context.
proactively resolve issues; issue resolution
What They're Looking For.
Must Have
Doctorate Degree, Master’s Degree and 2 years of life science, computer sciences, business administration experience, Bachelor’s degree and 4 years of life science, computer science, business administration experience, Associate’s degree and 8 years of life science, computer science, business administration experience, High school diploma / GED and 10 years of life science, computer science, business administration experience
Nice to Have
5 years’ work experience in life sciences or medically related field, 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company, Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials, Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
What You'll Do.
management and oversight of data collected within a study/program
lead end-to-end data management
and decision-ready data
Serve as the single accountable leader for study-level data management
and cross-functional alignment
Lead development and execution of the Data Management Plan and Integrated Data Review Plan (IDRP) aligned to protocol and program strategy
and go-live readiness in partnership with Database Design and Acquisition teams
Oversee study conduct activities including data cleaning
and database lock preparation
Monitor study data metrics (e.g.
Non-CRF data collection
reconciliation backlog
proactively resolve issues to ensure on-time delivery
Lead data deliverables
proactive in follow up
ensuring issue resolution and high-quality outputs
How You'll Work.
Team & Collaboration
cross-functional alignment; partnership with Database Design and Acquisition teams; engaging and working across clinical trial teams in multiple geographies
Communication Scope
cross-functional alignment; engaging and working across clinical trial teams
Process & Methodology
management and oversight of data collected within a study/program, lead end-to-end data management, Lead development and execution of the Data Management Plan and Integrated Data Review Plan (IDRP), Oversee study conduct activities, Lead data deliverables
Full Job Description
## **Career Category** Clinical ## ## **Job Description** **Join Amgen’s Mission of Serving Patients** At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Data Delivery Lead** **What you will do** Let’s do this. Let’s change the world. In this vital role you are accountable for the management and oversight of data collected within a study/program, you will lead end-to-end data management and ensure high-quality, timely, and decision-ready data that enables successful clinical trial delivery. * Serve as the single accountable leader for study-level data management, driving quality, delivery, and cross-functional alignment, locally and globally * Lead development and execution of the Data Management Plan and Integrated Data Review Plan (IDRP) aligned to protocol and program strategy * Drive database build, UAT, and go-live readiness in partnership with Database Design and Acquisition teams * Oversee study conduct activities including data cleaning, query management, reconciliation, and database lock preparation, ensuring we are ‘delivery ready’ at all times * Monitor study data metrics (e.g., eCRF entry, Non-CRF data collection, query agi
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