Clinical Scientist Director – Early Development, Oncology Job at Amgen (Lisbon)

New

Clinical Scientist Director – Early Development, Oncology

In this vital role, the Clinical Scientist Director will support early phase cli...

Location

Portugal , Lisbon

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of life sciences/healthcare experience
Master’s degree and 7 years of life sciences/healthcare experience
Bachelor’s degree and 9 years of life sciences/healthcare experience
5 years of pharmaceutical clinical drug development experience
Industry or academic experience in early-phase drug development within Oncology
Strong communication & presentation skills in English
Experience with designing, monitoring, and implementing clinical trials for Oncology and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements
Understanding of conducting study data readout activities, including data cleaning, database lock, data extract, producing outputs of data
Experience drafting high level submission documents for regulatory submissions including authoring clinical regulatory responses for health regulatory interactions
Serving as a contributing author to scientific publications and data presentations at scientific conferences

Job Responsibility

Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
Provide clinical input into & implementation of clinical trial(s), their delivery, clinical data review, interpretation of results
Review and analyze clinical trial data to ensure accuracy, completeness and adherence to protocol and regulatory requirements
Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

What we offer

Vast opportunities to learn, develop, and move up and across our global organization
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
Flexible work arrangements

Medical Director, Hematology

Lead the science that shapes tomorrow's hematology breakthroughs. Proclinical is...

Location

United States , Boston

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Medical degree (MD or equivalent), ideally with Hematology/Oncology fellowship training
Strong interest in developing innovative therapies and impacting patient populations
Experience in clinical research or drug development, spanning Phases I through IV, is preferred
Medical and scientific expertise in hematology or oncology is advantageous
Excellent collaboration and communication skills to work effectively with diverse teams and stakeholders

Job Responsibility

Lead clinical deliverables for a designated section of a clinical program with minimal supervision
Manage operational aspects and ensure successful execution of the clinical program in partnership with global line functions, Clinical Scientists, and Clinical Operations teams
Support and occasionally lead interactions with external collaborators, including regulatory authorities, key opinion leaders, advisory boards, and patient advocacy groups
Collaborate with internal teams such as Research, Early Clinical Development, Medical Affairs, Marketing, and HEOR
Contribute to Global Clinical Development training programs, author or review clinical SOPs, and participate in taskforces or panels to shape clinical development strategies

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Clinical Scientist Associate Director - Late Development, Oncology

In this role, the Clinical Scientist Associate Director supports late-phase clin...

Location

Portugal , Lisbon

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 3 years of life sciences/healthcare experience
Master’s degree and 5 years of life sciences/healthcare experience
Bachelor’s degree and 7 years of life sciences/healthcare experience
3 years of pharmaceutical clinical drug development experience
Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
Industry or academic experience supporting early or late-phase drug development within a relevant therapeutic area or disease indication
Strong communication and presentation skills in English
Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements
Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and generation of clinical data outputs
Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance

Job Responsibility

Support set up and execution of late phase clinical trials with a focus on data quality
Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
Provide input into & implementation of data management plan, CRF design, and data review oversight
Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
Assists Development Lead and Medical Sciences Director in medical monitoring and management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
Anticipate and actively manage problems across a broad spectrum of cross-functional teams
Work cross functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Support appropriate training, recruitment, and development requirements for matrix team resources

What we offer

Vast opportunities to learn, develop, and move up and across our global organization
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
Flexible work arrangements

Fulltime

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Creature Assistant Technical Director

We have an exciting opportunity for an enthusiastic artist interested in pursuin...

Location

Australia , Melbourne

Salary:

Not provided

Weta Digital

Expiration Date

Until further notice

Requirements

Excellent communication and organizational skills
Experience with Maya, rigging and animation
Experience with simulation of cloth and hair
Solid problem-solving skills
The ability to multi-task and prioritize across multiple projects
Basic working knowledge of Linux

Job Responsibility

Provides support to the Creatures team and aids in the process of getting work through the production pipeline
Supports multiple shows at a time and serves to ensure animation and creature work is flowing smoothly from one department to the next
Troubleshoots and solves issues and directs questions and problems to the appropriate TD where necessary

What we offer

Diversity of work
Exciting development opportunities
Dynamic working environment
Thriving and supportive workplace
Welcomed, respected, supported and appreciated environment
Workplace experience that’s second to none

Fulltime

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Join a top-tier, fee-based wealth management firm known for rigorous investment ...

Location

United States , Walnut Creek

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

3+ years in wealth management, including 2+ years building financial plans
CFP required
Strong knowledge across core planning disciplines
Experience with tools like eMoney, MoneyGuidePro, Holistiplan, WealthStudios, or Salesforce
Advanced Excel skills and strong communication abilities
Comfortable in a fast-paced, feedback-driven environment

Job Responsibility

Analyze client data and develop tailored financial planning recommendations
Attend meetings as the planning specialist and support advisors directly
Build and help implement complex financial plans
Provide guidance on estate, tax, retirement, cash flow, Social Security, pensions, and equity compensation
Maintain planning data across platforms and improve internal processes
Share planning updates and best practices with advisor teams

What we offer

Strong work-life balance
Three weeks of PTO
Fully paid medical, dental, and vision
Generous 401(k) match
Meaningful long-term growth

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We’re on the lookout for a Team Leader to support the Wigston Home Store. If you...

Location

United Kingdom , Wigston

Salary:

13.23 GBP / Hour

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Demonstrable evidence of behaviour in line with the core values of TAAS throughout career to date
Able to demonstrate effective people management experience
Collaborative approach to achieving departmental and wider organisational objectives
Passion for the work that TAAS does
Experience working in the retail or charity sector preferred
Passion for delivering exceptional customer service
Target driven and able to inspire a team
Experience as a sales assistant or retail supervisor preferred

Job Responsibility

Maximise sales and profits of your department within the store
Responsible for guiding and managing a group of individuals, both employees and volunteers to achieve specific goals and objectives
Provide direction, support, and motivation to the team members, delegate tasks, monitor progress, and ensure effective communication within the team
Proactively support and encourage both personal and professional development of your team
Ensure the day-to-day running of the department, including compliance with company guidelines and standards, and delivering exceptional customer service
Hold responsibility for Health & Safety and Environment, Safeguarding, Data Protection, Equality, Diversity, and Inclusion, Quality in your specialism

What we offer

Enhanced annual leave, with even more added as your service grows
Additional annual leave purchase options
Enhanced sick pay
Life assurance
Blue Light Card eligibility and access to generous discount schemes
A supportive, purpose-driven team
Access to our comprehensive Employee Assistance Programme

Parttime

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This role supports retail operations by engaging customers and facilitating thei...

Location

United States , Lampasas

Salary:

18.00 USD / Hour

T-Mobile

Expiration Date

Until further notice

Requirements

High School Diploma/GED
6 months of customer service and/or sales experience
Retail environment preferred
Passionate customer advocate
Competitive drive and proven ability to succeed in a fast-paced sales environment
Willingness to work alongside peers and store leaders
Effective at balancing customer needs and performance goals
At least 18 years of age
Legally authorized to work in the United States

Job Responsibility

Develop proficiency in customer service and sales to deliver personalized technology and service solutions
Utilize digital tools to demonstrate network coverage, service plans, and product features
Complete required training to build knowledge of retail processes, systems, and wireless technology innovations
Collaborate with colleagues across channels to support a seamless customer experience
Also responsible for other duties/projects as assigned by business management

What we offer

Competitive base salary and compensation package
Annual stock grant
Employee stock purchase plan
401(k)
Access to free, year-round money coaches
Medical, dental and vision insurance
Flexible spending account
Paid time off
Up to 12 paid holidays
Paid parental and family leave

Parttime

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Trades Manager - Engineering

Inspects construction performed by contractors at the Medical University of Sout...

Location

United States , Charleston

Salary:

57700.00 - 103900.00 USD / Year

MUSC Health

Expiration Date

Until further notice

Requirements

A high school diploma and four years professional experience directly related to the area of employment
Ability to obtain and maintain a valid driver’s license
Physical requirements: Ability to perform job functions in an upright position
Ability to perform job functions while walking/mobile
Ability to climb
Ability to work indoors
Ability to work outdoors in all weather and temperature extremes
Ability to work below ground
Ability to work in confined/cramped spaces
Ability to perform job functions from kneeling positions

Job Responsibility

Inspects construction performed by contractors at the Medical University of South Carolina to ensure that work complies with the plans and specifications and has been done in accordance with pertinent codes, regulations, and standards of craftsmanship
Prepares reports detailing results of inspections, problems encountered and solutions devised
Plans and coordinates outages with customers and provides general supervision of construction work done by contractors and MUSC forces on alteration and repair projects
Ensures that work is done in accordance with plans and specifications in a timely and efficient manner with minimum adverse impact on existing, adjacent occupants

Fulltime

Clinical Scientist Director – Early Development, Oncology

Amgen

Location:
Portugal , Lisbon

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 20, 2026

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