Study Delivery Resource Management Manager Job at Amgen (Cambridge)

Manager, Study Delivery Resource Management

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States

Salary:

113878.00 - 139695.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of clinical execution experience
Bachelor’s degree and 4 years of clinical execution experience
Associate’s degree and 8 years of clinical execution experience
High school diploma / GED and 10 years of clinical execution experience

Job Responsibility

Support end-to-end study delivery resourcing across clinical programs and countries
Contribute to forecasting, recruitment, resource allocation, deployment, and Full-Service Provider (FSP) oversight
Develop, maintain, and continuously improve reusable, automated reports and dashboards to track resource capacity, utilisation, and allocation trends
Leverage AI, analytics, and visualisation tools to identify patterns, predict resourcing needs, and flag potential risks or inefficiencies
Summarise analysis into concise, actionable insights
Serve as the single point of accountability for managing resource allocations at a program level
Effectively prioritize allocation of resources when competing demands arise
Continually horizon scan and collaborate closely with SDRM colleagues to manage upcoming resourcing risks & challenges
Manage complex or sensitive allocation situations diplomatically
Partner with HR and Talent Acquisition to manage the hiring process

What we offer

Total Rewards Plan
Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
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

Fulltime

Senior Manager, Study Delivery Resource Management (SDRM)

In this vital role, you will provide strategic oversight for resource planning a...

Location

United States

Salary:

170076.00 - 196130.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of clinical execution experience
Master’s degree and 6 years of clinical execution experience
Bachelor’s degree and 8 years of clinical execution experience
Associate’s degree and 10 years of clinical execution experience
High school diploma / GED and 12 years of clinical execution experience
Minimum of 2 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources

Job Responsibility

Provide strategic oversight for resource planning and allocation across global clinical programs and countries
Lead the development of accurate, forward-looking resource forecasts & hiring plans
Analyze historical and real-time data to identify trends, anticipate capacity gaps, and identify opportunities & mitigations
Serve as the single point of accountability for ensuring consistent, equitable, and strategically aligned resource allocation decisions
Develop, own and oversee hiring plans in partnership with HR and GDO SPOs
Provide leadership oversight for the FSP engagement model
Act as the trusted liaison to functional leadership, program partners, and country resource points of contact
Lead cross-functional process improvement initiatives

What we offer

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

Fulltime

Study Delivery Resource Management Senior Manager

Provide strategic oversight for resource planning and allocation across global c...

Location

United Kingdom , Uxbridge; London

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Degree educated
Proven ability to lead teams, manage complex projects or programs, and support effective resource coordination
Previous experience in Life Sciences, especially in Biopharmaceutical Clinical Research
Experience managing teams across multiple geographies
Experience overseeing CROs and other clinical vendors
Strong understanding of global clinical trial operations and resource management

Job Responsibility

Lead development of accurate, forward-looking resource forecasts and hiring plans at program, study, and country levels
Serve as the single point of accountability for equitable and strategically aligned resource allocation decisions
Develop and oversee recruitment strategies in partnership with HR and GDO SPOs
Provide leadership oversight for FSP engagement models and facilitate FMT governance
Act as a trusted liaison to senior functional leaders and country stakeholders
Lead cross-functional process improvement initiatives, integrating AI and automation where appropriate

What we offer

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

Study Delivery Senior Manager

In this vital role, you will own global clinical trial delivery, translating pro...

Location

United Kingdom , Cambridge; London; Uxbridge

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Degree educated
Clinical trial execution experience and previous people leadership managing teams, projects, resources or directing the allocation of resources
Previous experience in life sciences or a related field, including biopharmaceutical clinical research
Previous management experience of direct reports across multiple geographies
Experience representing a sponsor company in regulatory audit/inspections
Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)

Job Responsibility

Leading cross-functional study teams to deliver clinical data aligned with evidence generation strategy
Defining and executing study plans covering feasibility, site selection, site engagement, recruitment, retention, and vendor delivery
Identifying and managing study risks using quality-by-design and risk-based approaches to protect participant safety and data integrity
Overseeing global study execution, including enrollment, data flow, monitoring, and corrective actions
Providing clear leadership, issue resolution, and escalation management across geographies
Partnering effectively with internal stakeholders and external vendors to ensure performance and collaboration
Driving continuous improvement, innovation, and regulatory compliance throughout the study lifecycle

What we offer

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

LSOM Line Manager (Local Study Operations Line Manager)

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part...

Location

Taiwan , Taipei

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree & 2 years of clinical execution experience OR Master’s degree & 6 years of clinical execution experience OR Bachelor’s degree & 8 years of clinical execution experience OR Associate’s degree & 10 years of clinical execution experience OR High school diploma / GED & 12 years of clinical execution experience
In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources.

Job Responsibility

Lead the skill development of Local Study Operations Managers, ensuring effective trial implementation within the country and strong alignment with global strategies
Oversee the delivery of the country’s study portfolio—managing scope, timelines, and budgets—through the leadership of LSOM
Working in close partnership with the Country GSSO Head, help foster, enhance, and sustain an optimal clinical research environment that supports global R&D objectives
Drive alignment and continuous improvement in LSOM execution by integrating best practices, promoting digital innovation, and facilitating robust knowledge sharing across the team
Ensure the successful delivery of the study portfolio assigned to LSOMs
Oversee LSOMs’ fulfillment of responsibilities throughout the assigned country portfolio, from feasibility through to study close-out
Monitor portfolio progress, provide risk and quality oversight, and support issue escalation and resolution for LSOMs
Manage LSOM and LSOM vendor performance to guarantee high-quality study execution, serving as the primary escalation point for local study challenges, driving solutions, and ensuring portfolio targets are met within the country
Mentor, train, and support the professional development of LSOMs to prepare them for managing complex trials
Build and maintain a high-performing team

What we offer

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

Fulltime

Global Study Manager

Global Study Manager – This position is a fully client-embedded role, dedicated ...

Location

Poland

Salary:

Not provided

myGwork - LGBTQ+ Business Community

Expiration Date

Until further notice

Requirements

Bachelor’s degree: life sciences or related discipline
At least 5+ years of relevant study management experience on a global level
In-depth experience in clinical research: study management, monitoring, data management
Must have exposed to clinical study management “end-to-end” Globally : NA, EMEA, APAC, LATAM – China & Japan, Africa is an asset
Must have proven experience from study feasibility to CSR
Must have at least Ph II and PIII experience – PI & PIV is an asset
Must have cross-functional leadership proven experience, able to drive internal and external meeting
Able to input in clinical protocol, ICF, and other study plan, savvy in clinical study risk management and clinical systems
Strong experience in clinical budget management
Strong experience with vendor management including CRO

Job Responsibility

Accountable for delivering the clinical operation activities of the study until study archiving
Generating robust and accelerated delivery plans (with a focus on upper quartile performance) and delivering these to target or stretch thresholds and with quality
Accountable for the operational delivery of clinical study/studies to time, quality, and budget, company standards and scientific requirements, supporting decision -making at pace and leading study team to achieve overall study deliverables
Accountable for the following deliverables: Study Initiation Meeting, Clinical Study Activity Plan, Study Delivery Plan, TMF Quality Strategy Document, DCT Set Up, Vendors Oversight Plan, Investigator/CRA Meeting Set Up & associated training, Recruitment Tracking, Budget tracking eTMF filing and Vendor Set Up and Management, Safety Management plan, eTMF & vendor set -up
Proactively and effectively identifies, oversees, and mitigates study risks
Ensures appropriate stakeholder communication, including study status, expectations, risks and issues
Accountable to operate within the study budget
Effectively leads empowered matrix teams
Responsible for operational input into protocol and informed consent form development, and other key study documents
Leads and conducts investigator meetings and other study related meetings

Fulltime

Clinical Study Manager

Lead global rare‑disease trials that shape the future of patient care through ex...

Location

Sweden , Stockholm

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

University degree in Life or Health Sciences
Extensive knowledge of the clinical study process, including planning, conducting, and reporting multicenter international studies
Proven ability to lead multidisciplinary teams, with strong team-building, negotiation, and conflict resolution skills
Experience managing global clinical outsourcing and working with external service providers
High level of proactivity, commitment, and energy
Strong leadership, coaching, and interpersonal skills
Excellent problem-solving abilities and a customer-oriented mindset
Strong organizational and multitasking skills
Proficient in written and oral communication in English

Job Responsibility

Build relationships with investigators, study site personnel, external service providers (ESPs), and other stakeholders to ensure operational feasibility and understanding of patient needs
Lead and manage cross-functional clinical study teams, ensuring objectives and responsibilities are met
Oversee all clinical study activities, ensuring adherence to timelines, budgets, and quality standards
Ensure a quality database lock and completion of the Clinical Study Report
Identify and document risks related to clinical study activities and deliverables
Set up and maintain clinical tracking tools and study contact lists throughout the study lifecycle
Forecast and manage study budgets and contracts
Coordinate activities related to Investigational Medicinal Products, including ordering, labeling, distribution, and expiry date extensions
Ensure delivery and proper archiving of key clinical study documents
Define the scope of work for ESPs and oversee their performance, ensuring compliance with applicable guidelines and regulations

Senior Manager – Delivery Services

Completely manage a client account ensuring the right balance between delivery o...

Location

India , Kochi;Trivandrum

Salary:

Not provided

Experion Technologies

Expiration Date

Until further notice

Requirements

Completely manage a client account ensuring the right balance between delivery of ongoing projects and skills to maintain the customer relationship to identify new prospective projects from the client account
Experience and confidence in client management with good articulation, detailing and negotiation skills
Capable in coordinating client interactions for product requirement grooming and detailing, product development with modern engineering practices, user acceptance testing, rollout and release phases
Experience in Product Development in Web/Mobile technologies with industry standard engineering practices (CI/CD, DevOps, Automated Testing, Unit Testing through Code, Automated Review Gates etc.)
Passionate about going into functional and technical details along with inspiring, participating and motivating the core team in design/solutioning phases. Confidence to collect required details and present the same to client stakeholders
Expertise in handling end-to-end project delivery in Agile Methodology with hands on experience in Product Grooming, Agile Ceremonies, Collaborating with Technical Architects, Development, Testing, Release and Maintenance of the product
Excellent Project Management skills including Estimation, Scheduling, Tracking, Commercials and Quality
Experience in managing teams of size > 20 in a global delivery model
Experience in leading Agile teams anchoring different ceremonies like grooming, sprint planning, sprint retro and sprint demo
Excellent team management skills, enabling each team member to improve their competencies and work quality, and become better professionals

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Study Delivery Resource Management Manager

Job Description

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