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 creative 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.
ABOUT THE ROLE
Role Description:
The Study Delivery Associate provides essential administrative and operational
support to clinical trial management activities. This role supports the Study
Delivery Team in meeting study timelines, ensuring regulatory compliance, and
executing standardized processes related to clinical trial
coordination, document and system management.
The Study Delivery Associate may also support specialized activities to
promote expertise, quality,
and consistency across studies. Key responsibilities
include maintaining accurate and timely data within clinical systems (e.g.,
CTMS) and supporting study training and related operational requirements.
Roles & Responsibilities:
Study Coordination
* Support the setup and maintenance of study-level trackers, dashboards and
timelines.
* Communicate study progress, timelines and deliverables to the Study Delivery
Manager.
* Assist with tracking and following up on study actions, including risk
mitigation actions.
* Assist with the preparation and record keeping of risk & quality reviews.
* Ensure completion of study team training and inspection readiness activities
to maintain compliance with regulatory requirements.
* Assist with trial-related events, global site communications,
and logistics for investigator meetings
* Support study start-up activities, including system setup, supplier access
management, ICF track
📌 Study Delivery Sr Associate (Hyderabad)
🏢 AMGEN
📍 Hyderabad
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