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Senior Associate Operations (1-Year Contract)

Amgen


Job Location:

Hong Kong - Hong Kong

Monthly Salary: Not provided by the employer
Posted: 22 August 2026 (23 days ago)
Application Deadline: 19 November 2026
Vacancies: 1 Vacancy

Job Summary

Career Category
Medical Affairs
Job Description

Join Amgens Mission of Serving Patients

At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980 weve helped pioneer the world of biotech in our fight against the worlds 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 youll 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 lie within them youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Live

What you will do

Amgen is one of the worlds leading independent biotechnology companies. For over 4 decades Amgen has pioneered biotechnology breakthroughs to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring for a Senior Associate Operations (12-month contract with possibility of extension) for Amgen Hong Kong.

Live

What you will do

Roles and responsibilities:

Clinical Study Planning & Coordination for General Medicine

  • Lead the development and maintenance of study-level trackers dashboards timelines and tools (e.g. vendor management sample tracking drug supply planning) to ensure accuracy and visibility.
  • Coordinate logistics for quarterly steering committee and investigator meetings trial events and site communications.
  • Manage assigned start-up activities including system setup access management and document readiness ensuring completion to required standards.

Clinical Study Execution & Oversight

  • Use study dashboards and reports to monitor enrolment data flow and quality indicators taking proactive action to address deviations and risks.
  • Lead delivery of assigned risk and quality management activities
  • Track and report study progress budget management coordinating with steering committee team and vendors to resolve operational issues and maintain compliance.
  • Deliver assigned components of recruitment and retention strategies to help ensure enrolment targets are achieved.

Stakeholder Engagement & Team Collaboration

  • Build and maintain effective relationships with internal study team members vendors and investigator sites
  • Act as a point of contact for routine study updates ensuring stakeholders are informed and aligned.
  • Identify prioritize and escalate risks effectively to support swift informed decisions

Medical event planning and coordination

  • Provide administrative support across medical therapeutic areas under both business units: General Medicine (Inflammation Cardiovascular Bone Rare Disease) and HONC (Haematology and Oncology) to ensure tasks completion and compliant to Amgen policies and SOPs
  • Responsible forprocure-to-pay function for the assigned teams
  • Track expenses for the assigned teams against budget
  • Assistwith project development and planning to ensure efficient execution and organization
  • Assistmedical teams in implementation of activities and key events
  • Local Regulatory Affairs provides country regulatory expertise and execution for the development registration and lifecycle management of all Amgen molecules.

Win

What we expect of you

Basic qualification:

  • Medical or scientific education or experience from similar positions or industry Pharmaceutical industry experience will beadvantageous
  • Minimum 2-3 years of experience as a research assistant or clinical trial assistant or clinical study management experience is preferred
  • Experience in administrative management and logistics planning is preferred

Thrive

What you can expect of us

As we work to develop treatments that take care of others we work to care for our teammates professional and personal growth and well-being

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health finance and wealth work/life balance and career benefits

Amgen is an Equal Opportunity employer and will consider you without regard to your race color religion sex sexual orientation gender identity national origin protected veteran status or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Apply now for a career that defies imagination

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Required Experience:

Senior IC


About Company

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Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the ... View more

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