Study Liaison Senior Associate

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s 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, you’ll 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 lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Study Liaison Senior Associate

What you will do

Let’s do this. Let’s change the world. In this vital role you will accountable for the development of GPS strategy for safety-related organized data collection in Amgen clinical trials in compliance with global regulatory requirements and Amgen compliance policies and standards.

Accountable for the review, approval, and execution of GPS safety data collection strategy across clinical programs (e.g. interventional, observational research, non-Amgen sponsored clinical research, post-trial access, expanded access, etc.).

Responsible for participating in cross-functional activities to ensure and promote compliance with pharmacovigilance data collection standards and operational consistency across clinical programs for all Amgen products.

Job Summary

The Senior Associate works on projects and processes that ensure the strategies of the department are driven into the safety related organized data collection activities in Amgen clinical trial activities to ensure Amgen remains aligned with global safety legislation and requirements.

Key Activities

Responsibilities include:

• Aids in various administrative tasks regarding project activities and schedules.

• Keeps information up to date including schedules and the project information in appropriate applications.

• Perform tasks with minimal direction, in addition to working on teams to accomplish tasks.

• Various administrative tasks regarding project activities and schedules and posting items to project folders.

• Coordination with the project team and project manager.

• Provide technical support to ensure the execution of the group’s objectives.

• Provide assistance and input to the development of protocols, contracts, safety management plans, and investigative site study guidance documents

• Supports clinical reconciliation activities and vendor oversight to ensure reporting of all reportable safety event data within team’s remit.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a with these qualifications.

Preferred Qualifications:

• Demonstrates analytical skills to solve day-to-day problems

• Applies a methodical approach to completing all tasks

• Demonstrates solid written and oral communication skills

• Demonstrates Amgen Values and clearly presents information (spoken or written)

• Communicates at various organizational levels and listens actively

• Applies a consistent approach to planning and organizing tasks

• Demonstrates ability to perform accurate and detailed work

• Demonstrates excellent ability to learn quickly and understand/adapt quickly to new systems, processes, and tools

• Organized, reliable, and responsive.

Basic Qualifications:

Master’s degree

OR

Bachelor’s degree and 2 years of Pharmaceutical Industry experience

OR

Associate’s degree and 6 years of Pharmaceutical Industry experience

Or

High school diploma / GED and 8 years of Pharmaceutical Industry experience

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

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As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided 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 accommodation.