Study Delivery Associate

HYDERABAD (IN)ONSITEPOSTED: 6/29/2026
PHARMAFull-time
HIRING ORGANIZATIONAMGENBiotechnology / Pharmaceuticals
Amgen

ROLE DEFINITION & RESPONSIBILITIES

Support global clinical trial execution and operational excellence. Responsibilities include:

Support study setup activities and timelines
Maintain study trackers and operational dashboards
Assist Study Delivery Managers with project coordination
Maintain inspection readiness documentation
Coordinate investigator meetings and study logistics
Maintain CTMS records and support eTMF documentation
Manage study training records
Prepare clinical study documents
Support regulatory submissions

REQUIRED VERIFIED SKILLS

Clinical Trial Management Systems (CTMS)
Electronic Trial Master File (eTMF)
Electronic Data Capture (EDC)
Trial Master File (TMF)
Clinical Documentation
Regulatory Documentation
Microsoft Excel
Microsoft Word
Microsoft PowerPoint
Clinical Trial Compliance
Investigator Documentation
Protocol Management
Global Study Coordination
Risk Management
Study Start-up Activities
Vendor Management
Clinical Data Management
Inspection Readiness

COMPENSATION & REWARDS

8.0L - 13.5L per annum
Ensure you highlight experience with CTMS, eTMF, and clinical trial compliance. The role favors candidates with a background in CRO, Biotech, or Pharma environments.

ORGANIZATION CONTEXT & CULTURE

Amgen is a leading global biopharmaceutical company committed to unlocking the potential of biology for patients suffering from serious illnesses. It discovers, develops, manufactures, and delivers innovative human therapeutics, focusing on areas with high unmet medical needs such as oncology, cardiovascular disease, bone disease, and inflammatory diseases.

TEAM SIZE: 25,000+ employees
INDUSTRY: Biotechnology / Pharmaceuticals

EXPECTED CAREER ROADMAP

The estimated salary range is based on current market trends for similar Clinical Operations roles in Hyderabad. Actual compensation may vary depending on experience, skills, and internal compensation policies.

READY TO SUBMIT?

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