Amgen has announced a new opportunity for the position of Study Delivery Associate in Hyderabad, India. This is an excellent opportunity for candidates looking to build a career in Clinical Operations, Clinical Research, and Clinical Trial Management within one of the world’s leading biotechnology companies.

If you have experience in clinical trial coordination, CTMS, eTMF, TMF management, clinical documentation, and study operations, this role offers the chance to work on global clinical studies while supporting innovative therapies that improve patient lives.

Whether you’re currently working in a CRO, pharmaceutical company, or biotech organization, this Amgen Study Delivery Associate job in Hyderabad could be your next career move.

Amgen Study Delivery Associate Job Overview

About Amgen

Amgen is one of the world’s leading biotechnology companies focused on discovering, developing, manufacturing, and delivering innovative medicines. With over four decades of scientific innovation, Amgen combines biology, genetics, and technology to develop treatments for serious diseases across multiple therapeutic areas.

Working at Amgen provides exposure to global clinical development programs, advanced clinical technologies, and collaborative international teams.

Key Responsibilities

As a Study Delivery Associate, you will support global clinical trial execution and ensure operational excellence throughout the study lifecycle.

Clinical Study Coordination

• Support study setup activities and study timelines
• Maintain study trackers and operational dashboards
• Assist Study Delivery Managers with project coordination
• Track study milestones and action items
• Support risk mitigation activities
• Maintain inspection readiness documentation
• Coordinate investigator meetings and study logistics
• Assist with site communications
• Support vendor coordination
• Manage investigational product logistics
• Coordinate biological sample shipment and reconciliation

Clinical Trial Systems Management

• Maintain CTMS records
• Support eTMF documentation
• Manage study training records
• Ensure timely data entry
• Process system access requests
• Maintain accurate clinical trial databases

Documentation & Regulatory Support

• Prepare clinical study documents
• Support regulatory submissions
• Maintain monitoring plans
• Support Trial Master File (TMF) filing
• Ensure essential documents remain inspection-ready
• Maintain protocol documentation
• Support informed consent documentation tracking

Continuous Improvement

• Participate in process improvement initiatives
• Share operational best practices
• Support quality compliance activities
• Collaborate with global study teams

Educational Qualifications

Candidates should possess one of the following:

• Bachelor’s Degree

OR

• Associate Degree with 4 years of clinical execution experience

OR

• High School Diploma/GED with 6 years of clinical execution experience

Preferred Experience

Amgen prefers candidates with:

• 2+ years in Life Sciences or Healthcare
• At least 1 year of Biopharmaceutical Clinical Research experience
• Experience in CRO, Biotechnology, or Pharmaceutical companies
• Exposure to Global Clinical Trials
• Clinical Operations experience
• Clinical Trial Coordination knowledge

Required Skills

Successful candidates should have experience with:

• 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

Why Join Amgen?

Working at Amgen offers several advantages:

• Global biotechnology leader
• Opportunity to work on international clinical trials
• Career growth in Clinical Development
• Exposure to cutting-edge biotechnology
• Collaborative work environment
• Professional development opportunities
• Competitive salary and employee benefits
• Strong learning and innovation culture

Expected Salary

Based on current market trends for similar Clinical Operations roles in Hyderabad, the estimated salary range is:

₹8,00,000 – ₹13,50,000 per annum (CTC)

Actual compensation may vary depending on experience, skills, and internal compensation policies.

Who Should Apply?

This opportunity is ideal for:

• Clinical Research Associates (CRA)
• Clinical Trial Coordinators
• Clinical Operations Associates
• Study Coordinators
• Clinical Documentation Specialists
• TMF Specialists
• CTMS Coordinators
• CRO Professionals
• Life Science Graduates
• Pharmacy Graduates
• Biotechnology Graduates
• Clinical Research Professionals

How to Apply

Application Link