Sr Mgr Global Clinical Program Management
US - California - Thousand Oaks - Field/Remote, United States
Career Category
ClinicalJob Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.
Sr Mgr Global Clinical Program Management
Live
What you will do
Let’s do this. Let’s change the world. In this vital role you will oversee the planning and execution of global clinical trials. They work with cross-functional teams to ensure projects are completed on time and within budget while meeting quality standards.
Responsibilities:
- Supports the CPM-D in coordinating, overseeing the operational strategy, planning, risk assessment and mitigation, and overall execution of clinical trial programs globally (accountable for all studies in the program if no director level present)
- Line Management of GTMs
- Ensuring high-quality execution of clinical trials on time and within budget
- Supports / Leads the Global Clinical Study Team for the allocated program(s)
- Provides clinical operations leadership and expertise on the Evidence Generation Team (EGT) and in development of the Evidence Generation Plan (EGP) and provides clinical operations leadership and expertise in EGP execution through the feasibility and study design process
- Maintains global business relationships cross-functionally and communicates global status of clinical trial programs to senior management and oversight of study/ team issue escalation
- Initiates and supports conduct of Country Operational Landscape Assessments and study feasibility with Development Feasibility Senior Managers
- Supports / Accountable for study global enrolment plans revised enrolment plans and accurate global recruitment forecasting
- Reviews vendor evaluation to include identification of outsourcing requirements for study / program and oversee management of vendors
- Supports and oversees internal audit and inspection activities and contributes to CAPAs globally for the program
- Supports CPO resource planning for assigned program(s) in collaboration with Program Resource Management (PRM) and CPM-D
- Support continuous improvement initiatives in Clinical Program Operations and Global Development Operations (GDO)
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a Senior Manager with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of directly related experience or
Master’s degree and 4 years of directly related experience or
Bachelor’s degree and 6 years of directly related experience or
Associate’s degree and 10 years of directly related experience or
High school diploma / GED and 12 years of directly related experience
Preferred Qualifications:
- 9 years’ work experience in life sciences or medically related field, including 6 years of biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company
- Previous management experience of direct reports
- Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)
Thrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
Amgen offers a Total Rewards Plan comprising 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 including:
- 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.
- 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
- Flexible work models, including remote work arrangements, where possible
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
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 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.
.Salary Range
162,437.00 USD - 197,234.00 USD ApplyJob Profile
Field/Remote
Benefits/PerksAnnual bonus program Career development Career development opportunities Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Life and Disability insurance Personal growth Professional and personal growth Professional growth opportunities Remote work Remote work arrangements Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans
Tasks- Collaboration
- Conduct feasibility assessments
- Coordinate operational strategy
- Ensure project completion on time and within budget
- Lead continuous improvement initiatives
- Manage study teams
- Oversee global clinical trials
- Resource management
- Risk assessment and mitigation
- Study design
- Support vendor management
Biopharmaceutical BioTech Biotechnology Business Clinical operations Clinical program management Clinical Research Clinical trials Collaboration Continuous Improvement Cross-functional Collaboration Development Evidence Generation Execution Forecasting Insurance Leadership Life sciences Management Manufacturing Operational strategy Operations Pharmaceutical Program Management Project Management Quality Recruitment Recruitment Forecasting Research Resource Management Resource Planning Risk Assessment Sales Strategy Study Design Teams Vendor Management
Experience10 years 12 years 2 years 4 years 6 years 9 years
EducationAssociate Associates Bachelor's Degree DO Doctorate Doctorate degree GED High School High school diploma Life Sciences Master's
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9