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Study Delivery Sr Associate

Amgen
3+ years
Not Disclosed
Hyderabad
1 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment

Study Delivery Senior Associate

Location: Hyderabad, India
Work Type: On-Site

Position Summary

The Study Delivery Senior Associate provides critical global study management support to clinical study teams, ensuring timely, high-quality, and compliant study execution. This role partners closely with Study Managers to support study start-up, execution, risk monitoring, issue management, and operational oversight across the clinical trial lifecycle.

The position is assigned to individual study teams while also supporting multiple studies through specialized study management processes, providing broad exposure to global clinical trial operations.


Key Responsibilities

Study Planning & Coordination

  • Develop, maintain, and manage study-level trackers, dashboards, timelines, and operational tools.

  • Support vendor management, sample tracking, and drug supply planning activities.

  • Ensure study metrics and operational data remain accurate and up to date.

  • Coordinate logistics for investigator meetings, study events, and site communications.

  • Manage assigned study start-up activities, including:

    • System setup

    • User access management

    • Document readiness

  • Ensure all start-up activities are completed according to study timelines and quality standards.


Study Execution & Oversight

  • Monitor study dashboards and reports to track:

    • Global enrollment

    • Data flow

    • Study quality indicators

  • Proactively identify deviations, risks, and operational challenges.

  • Lead assigned risk management and quality oversight activities.

  • Track study progress and coordinate issue resolution with study teams and external vendors.

  • Ensure compliance with study plans, timelines, and regulatory requirements.

  • Support and execute assigned global recruitment and patient retention initiatives.

  • Manage study training system activities and associated oversight responsibilities.


Stakeholder Engagement & Collaboration

  • Build and maintain effective working relationships with:

    • Study team members

    • Functional partners

    • Vendors

    • Investigator sites

  • Serve as a key point of contact for routine study communications and updates.

  • Ensure stakeholders remain informed and aligned on study activities.

  • Identify, prioritize, and escalate risks to support informed decision-making and timely resolution.


Site & Vendor Management

  • Coordinate vendor onboarding and setup activities.

  • Lead vendor engagement activities to ensure quality, consistency, and timely delivery of services.

  • Monitor vendor performance and support issue resolution when required.


Data & Systems Management

  • Maintain and monitor clinical trial systems, including Clinical Trial Management Systems (CTMS).

  • Ensure accurate and timely data entry, tracking, and reporting.

  • Support data collection oversight activities, including:

    • Query management

    • Data reconciliation

    • Data review processes

  • Manage Trial Master File (TMF) documentation to maintain inspection readiness and compliance.


Process Improvement & Compliance

  • Contribute to continuous improvement initiatives across study operations.

  • Support development and sharing of best practices within the study management community.

  • Identify opportunities to streamline, automate, and optimize operational processes.

  • Support audits, inspections, and regulatory reviews.

  • Participate in Corrective and Preventive Action (CAPA) activities.

  • Facilitate implementation of lessons learned and process improvements across studies.


Basic Qualifications

Candidates must meet one of the following requirements:

  • Master's Degree, OR

  • Bachelor's Degree with a minimum of 2 years of clinical execution experience, OR

  • Associate Degree with a minimum of 6 years of clinical execution experience, OR

  • High School Diploma/GED with a minimum of 8 years of clinical execution experience.


Preferred Qualifications

  • Minimum 3 years of experience in life sciences, healthcare, biotechnology, pharmaceutical, or related fields.

  • At least 1 year of clinical research experience within:

    • Biotechnology companies

    • Pharmaceutical organizations

    • Contract Research Organizations (CROs)

  • Experience supporting or managing global clinical trials.

  • Knowledge of clinical trial operations and study management processes.

  • Experience with CTMS, TMF, and other clinical systems.

  • Understanding of risk management, quality oversight, and compliance requirements.

  • Familiarity with clinical trial documentation and inspection readiness activities.