Amgen

biotech

DataAcquisitionLead

Madurai, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Data Acquisition Lead at Amgen. Skills: acquisition, integration, and quality management of non-CRF (external/vendor) clinical trial data, management and oversight of external vendors. lead the acquisition, integration, and quality management of non‑CRF (external/vendor) clinical trial data. Own the design, setup, and ongoing management of non‑CRF data”

What You'll Achieve.

timely, accurate, and fit‑for‑purpose data to support study delivery, analytics, database lock, inspections, and regulatory compliance; seamless integration, traceability, and compliant ingestion into EDC and other clinical data systems; prevent downstream delays and ensure ongoing data delivery and analysis readiness; improve operational efficiency, scalability, data quality, and vendor integration performance

Industry & Context.

biotech
Problems you'll solve

effective problem-solving skills; problem-solving

What They're Looking For.

Must Have

Bachelor’s degree, 8 - 15 years of clinical execution experience

Nice to Have

8 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.

and quality management of non‑CRF (external/vendor) clinical trial data

and ongoing management of non‑CRF data

and maintain vendor data transfer specifications and agreements

and compliant ingestion of external datasets

Lead reconciliation activities

Own issue and query resolution for external data

Support database lock and inspection readiness

Drive process improvements

and standardization initiatives

How You'll Work.

Team & Collaboration

Partner closely with global and local cross‑functional study teams; collaboration abilities

Communication Scope

communication

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 Acquisition Lead** **What you will do** Let’s do this. Let’s change the world. In this vital role you will lead the acquisition, integration, and quality management of non-CRF (external/vendor) clinical trial data, ensuring it is timely, accurate, and fit-for-purpose to support study delivery, analytics, with regulatory compliance. * In this vital role, you will lead the **acquisition, integration, and quality management of non‑CRF (external/vendor) clinical trial data** , ensuring it is **timely, accurate, traceable, and fit‑for‑purpose** to support study delivery, analytics, **database lock, inspections** , and regulatory compliance. * Own the design, setup, and ongoing management of non‑CRF data (e.g., central labs, imaging, wearables, precision medicine), ensuring seamless integration, traceability, and compliant ingestion into EDC and other clinical data systems. * Own, define, and maintain vendor data transfer specifications and agreements, aligned with protocol, study requ

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