Sr Associate Project Manager - Remote
Career Category
Join Amgen ’s Mission of Serving Patients
What you will do
Responsibilities
- Provide project management to technical teams responsible for developing biosimilar candidates through to regulatory approval
- Provide project management of biosimilar business unit (BBU) analytical similarity sample management.
- Collaborate closely with cross-functional team including Similarity Team, Critical Regents Group (CRG), Data Management, and scientific staff to plan and maintain inventory.
- Manage logistics for distribution of samples for testing and communicate incoming data for biosimilar projects.
- Create electronic laboratory notebooks (ELN) for sample submission.
- Generate lot number, sample ID, and retrieving data in QC LIMS.
- Assist BBU staff with navigating ELN software and placing work orders for ELN updates. Database queries of LIMS, ELN and other databases including the compiling and organizing data to review, verify independently or in coordination with Data Management.
- Retrieve and organize data for review with Data Management
- Document archival in controlled document repository
- Provide data verification as needed for internal documents and regulatory filings in controlled document system.
- Utilize a strong foundation in scientific principles to thoroughly review regulatory documents and accurately determine the data elements that require verification in accordance with established protocols.
- Collaborate with cross-functional teams to ensure the completion and accuracy of the data verification processes.
- Assist in formatting documents in compliance with Amgen 's internal style guidelines and standards.
What we expect of you
Basic Qualifications
Master’s degree OR
Bachelor’s degree and 2 years of Project Management experience OR
Associate’s degree and 6 years of Project Management experience OR
Preferred Qualifications
- Experience supporting pharmaceutical research and development or nonclinical drug development programs within the biotechnology, pharmaceutical, or life sciences industry.
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Experience working with document management systems, collaboration platforms, and project management tools.
Experience coordinating scientific or regulatory documents throughout the document lifecycle.
Strong organizational skills with the ability to manage multiple priorities in a dynamic, fast-paced environment.
What you can expect from 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. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
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A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and bi-annual company-wide shutdowns
careers.amgen.com
Sponsorship for this role is not guaranteed.
Not included in the source posting: benefits.
Skills
Who can apply
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