Global Clinical Program Management Associate Director page is loaded
Global Clinical Program Management Associate Director
Apply remote type: Flex Commuter / Hybrid Locations: United Kingdom - Uxbridge, United Kingdom - Remote, United Kingdom - Cambridge Time type: Full time Posted on: Posted 2 Days Ago Job requisition id: R-204818 Career Category
Clinical Job Description
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. What you will do
Let’s do this. Let’s change the world. In this vital role you will be part of Clinical Program Operations (CPO) to plan and execute the operational aspects of clinical trials globally. Reporting to the Clinical Program Management Associate Director (CPM AD) will be the Global Trial Manager (GTM). Reports to: Clinical Program Management Director Therapeutic Area (TA): Obesity Responsibilities:
Supports the CPM-D in coordinating and 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 GCTMs. Ensures 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 oversees 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). 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 Sr. Manager with these qualifications. Basic Qualifications:
Degree in relevant field with life sciences or medically related experience work. Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Preferred Qualifications:
Experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company. Previous management experience with direct reports. Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.). What you can expect of us
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. LOCATION:
The successful candidate will have the ability to work flexibly from home with occasional office work from our Uxbridge or Cambridge next generation workspace. APPLY NOW
What we do is hard. It should be. We are working with each other against the challenges of today for the promise of tomorrow. Lead the way. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, 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. About Us
Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
#J-18808-Ljbffr
Apply remote type: Flex Commuter / Hybrid Locations: United Kingdom - Uxbridge, United Kingdom - Remote, United Kingdom - Cambridge Time type: Full time Posted on: Posted 2 Days Ago Job requisition id: R-204818 Career Category
Clinical Job Description
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. What you will do
Let’s do this. Let’s change the world. In this vital role you will be part of Clinical Program Operations (CPO) to plan and execute the operational aspects of clinical trials globally. Reporting to the Clinical Program Management Associate Director (CPM AD) will be the Global Trial Manager (GTM). Reports to: Clinical Program Management Director Therapeutic Area (TA): Obesity Responsibilities:
Supports the CPM-D in coordinating and 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 GCTMs. Ensures 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 oversees 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). 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 Sr. Manager with these qualifications. Basic Qualifications:
Degree in relevant field with life sciences or medically related experience work. Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Preferred Qualifications:
Experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company. Previous management experience with direct reports. Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.). What you can expect of us
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. LOCATION:
The successful candidate will have the ability to work flexibly from home with occasional office work from our Uxbridge or Cambridge next generation workspace. APPLY NOW
What we do is hard. It should be. We are working with each other against the challenges of today for the promise of tomorrow. Lead the way. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, 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. About Us
Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
#J-18808-Ljbffr
