lead, implement and communicate changes per the Change Impact Assessment Review & Approval process or other mechanisms as appropriate
partner with Resource Forecasting Group staff to support optimised planning of resources and budget
own the development of and supervise the implementation of high-quality, realistic, cross-functional, global clinical trial timelines, from design through final study reporting, in Amgen’s planning systems within specified deadlines
build scenario options in support of decision-making for operational or strategic direction
participate in process improvement initiatives as assigned
ensure alignment of funding/investment of clinical studies within assigned programs to support operational planning by functions
maintain accuracy of clinical study timeline information in Amgen data control systems , through conducting integrity checks and data issue resolution on a routine basis for assigned study timelines
communicate information on clinical trial status, changes, and issues to stakeholders, and confirm acceptance of clinical study timelines with functional representatives ensuring alignment with key operational goals and timelines
Requirements
degree educated
drug development knowledge with understanding of other functions, including Pre-Clinical, Clinical, Development Operations, and Regulatory
project management tools and processes
broad work experience in life sciences or medically related filed, including general biopharmaceutical clinical product development
marketing manager
Working hours
full-time
Requirements
proven project management experience, including budget and quality management
expertise in delivery of blended learning methods
strong influencing and collaboration skills to ensure effective partnership with stakeholders
experience of managing SharePoint sites and Teams channels
demonstrable experience in enabling marketing competencies for a business
experience in managing or quickly learning corporate systems such as LMS and Workday
experience in working with meeting management partners to deliver projects successfully
proven experience in understanding of business priorities to deliver improved marketer learning experiences
Responsibility
plan, manage, and implement multiple projects to ensure delivery that is on time, within budget, and of high quality, including establishing performance expectations and measurement plans
maintain updated documents and communications within Teams, SharePoint, and/or other platforms –particularly learning assets and associated collateral
commercial manager
Working hours
full-time
Requirements
degree educated in a relevant discipline, with proven experience within Pharmaceutical or Biotechnology
strong communication skills, with the ability to le to effectively represent ideas both verbally and in writing
extensive knowledge of the global safety environment, regulations and guidance, including compliance issues and/or scientific discovery
project and/or Process Management experience & knowledge
experience and knowledge of safety data capture, representation and interpretation
ability to work cross-functionally within matrix environment
strong organisation planning and prioritising workload
what you can expect of us
Responsibility
contribute to projects which involve the implementation of new processes and methods within and across Global Patient Safety
act as a representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility
provide knowledge into Clinical and Commercial teams on the needs and timelines of safety related organized data collection to ensure these needs are met and incorporated into Amgen studies and commercial activities/programs
operations manager
Working hours
full-time
Responsibility
career Category
administrative
lead or participate in the development, review and implementation of processes, policies, SOPs and associated documents affecting Data Management, including
congress Operations Logistics Manager
clinical Data Management Manager
amgen Global Study Operations team are looking for an experienced Clinical Data Manager to join our established team
if you are looking for your next career step in Project Management within Clinical Data management and want to be part of our mission - To serve patients - which drives all that we do, apply or get in touch
assign tasks within Case Management to direct and indirect reports
Requirements
relevant Bachelor’s degree
solid experience in/knowledge of data management in a pharma/biotech/CRO arena
bachelor’s degree or equivalent in life science, computer science, business administration
proven project management/lead and planning experience
master’s degree, Bachelors degree or Associates degree are preferred with directly related experience in PV
experience in RAVE EDC will be highly regarded
previous experience directly managing teams, projects, programs or directing the allocation of resources
demonstrated experience working effectively in cross-functional teams
team manager
Working hours
full-time
Responsibility
this role will drive the strategic design, build and execution of how Amgen approaches Congress participation, both in the virtual world as well as in a future hybrid in-person / virtual model
A strategic thinker, this person will be savvy in harnessing the power of technology, understanding drivers of HCP behaviors, and be adept at translating generated insights into intel that informs business strategy worldwide
this person will also understand Amgen’s internal cross-functional capabilities in the congress space, understand the incentives and objectives of each unique stakeholder, and effectively become a bridge between the Global Marketing and Medical Organizations
lastly, this person will be the critical link between the global organization and the local markets in understanding local needs and providing support in locally executed congresses as appropriate
business manager
Working hours
full-time
Language
english
Responsibility
how might you defy imagination
career Category
if you feel like you’re part of something bigger, it’s because you are
strategy and Innovation
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
exhibit leadership and expertise in addressing business issues and opportunities through relevant analytical approaches
Requirements
doctorate, Bachelor’s or Master’s degree and demonstrated pharmaceutical market analysis and/or business planning
proven ability to translate business questions and needs into relevant research plans and synthesize multiple data sources to answer business questions
demonstrated ability to translate business questions and needs into relevant research plans and synthesize multiple data sources to answer business questions
the ability to translate business questions and needs into research plans and synthesize multiple data sources to answer business questions
strong leadership experience in delivering results, shaping the future and developing capabilities in BAI
demonstrated ability to deliver results, champions new innovative methodologies and tools, and strengthen the ELMAC country community
champion new innovative methodologies and tools, and lead by influence to strengthen the ELMAC country community
champions new innovative methodologies and tools, and lead by influence to strengthen the ELMAC country community
senior project manager
Working hours
full-time
Responsibility
support the alignment of HEOR deliverables with the overall product plan
serve as a point of contact for project management related activities for HEOR global results
provide project information to HEOR Product Lead / TA Head for incorporation into portfolio-level strategy, plans, deliverables
shape processes to increase team efficiency and productivity
drive the development and execution of high quality, integrated, cross-functional timelines/plans for HEOR product deliverables aligned with the HEOR Book of Work
plan and prepare HEOR trainings with HEOR subject matter experts
ensure program/project key milestones are met by partnering with vendors, identifying risks and capacity restrictions, communicating program/project changes to the cross-functional teams
prepare reporting tools that document ongoing progress and activity
Requirements
degree educated in relevant field
proven experience in project management within Biotechnology, Pharmaceutical or another Healthcare related field
experience in HEOR or HTA
experience in change management and process improvement
experience in leading team, coaching and resource plans
experience in leading cross functional work, work effectively with colleagues and ability to navigate matrix organization
hr generalist
Working hours
full-time
Language
english
Responsibility
day to day management of key processes such as Immigration, Right to Work, Audit support - ensures SLA’s are adhered to by external vendors - managing contract renewal process with designated suppliers
operations manager
Working hours
full-time
Responsibility
career Category
administrative
lead or participate in the development, review and implementation of processes, policies, SOPs and associated documents affecting Data Management, including
congress Operations Logistics Manager
clinical Data Management Manager
amgen Global Study Operations team are looking for an experienced Clinical Data Manager to join our established team
lead and oversee projects and activities in support of Business Process Owner
own core process areas and proactively identify areas for improvement/efficiency
Requirements
relevant Bachelor’s degree
solid experience in/knowledge of data management in a pharma/biotech/CRO arena
bachelor’s degree or equivalent in life science, computer science, business administration
proven project management/lead and planning experience
master’s degree, Bachelors degree or Associates degree are preferred with directly related experience in PV
experience in RAVE EDC will be highly regarded
BA/BS/BSc or RN
previous experience directly managing teams, projects, programs or directing the allocation of resources
clinical services manager
Working hours
full-time
Requirements
registered Pharmacy Technician OR Registered Pharmacist with the General Pharmaceutical Council
practical experience in a clinical research setting working on complex clinical programs in a pharmacy at an investigational site
experience with drug formulations, sterile product compounding and administration practices
relevant therapeutic area education and training
knowledge of ICH/GCP regulations and guidelines
strong knowledge of clinical trial operations
computer and system operation skills
demonstrated ability to anticipate and resolve problems