Pharma Data Science Consultant Job at Amaris Consulting (Tokyo)

Life Science Consultant

Deallus are a global life-sciences management consultancy specializing in life s...

Location

United States , New York City

Salary:

105000.00 - 130000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Experience covering breast cancer area of disease
Familiarity, and in-market experience, with the US pharmaceutical market, through recent employment with US-based consulting firm
Advanced degree in medicine/ life sciences from leading global faculty (Ph.D. preferred)
Consultant level: 3+ years of relevant professional experience
Track record of professional success, with successive stages of advancement/ promotion
Proven Leadership skills (functional, team, client, team, etc.)
Experience in pharma competitive intelligence
Strong knowledge and hands-on competitive intelligence experience in the pharmaceutical industry, including issue monitoring and coverage of industry conferences, primary C.I., CI deep dives, workshops, scenario planning, and synthesis/ insight generation
Experience working on Commercial Strategy or Market Access projects
Preferably depth in one or more of the following therapeutic areas: Oncology, Neurology, Vaccines, Immunology, Cell & Gene, Rare Disease

Job Responsibility

Develops key project deliverables, such as discreet pieces of (qualitative, quantitative, financial, pharmaco-economic) research, analysis and synthesis
Using a range of strategic frameworks, conceptualizes complex data into compelling, succinct and actionable insights
Creates, adheres to, manages, project plan and budget, incl. key milestones, delivery timelines, review sessions, with an eye for available capacity and for potential issues and risks
Scopes out team role(s) and successfully delivers on own such role (including for example, project manager, financial/ quant analyst, communications champion)
Manages small team in executing client project(s), addresses performance concerns effectively and early on
Ensures high quality of deliverables, e.g., through four-eye principle, check list or formal quality control process
Conducts project reviews and provides / seeks formal feedback at the close of every project (or at contract renewal for monitoring projects) to ensure key learnings from the project are captured
Interacts with defined client teams in communicating progress, questions / hypotheses / conclusions, in addressing any questions and concerns, and in flagging issues as needed
Ensures client satisfaction throughout the term of the project
Takes on practice leadership role, e.g., related to recruiting, knowledge management, pursuit leadership

What we offer

In addition to a rewarding career, we support our GlobalData Heathcare colleagues with a range of benefits across health, finances, fitness, travel, tech and more

Fulltime

Life Science Consultant

Deallus are a global life-sciences management consultancy specializing in life s...

Location

United States , New York City

Salary:

105000.00 - 130000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Experience covering breast cancer area of disease
Familiarity, and in-market experience, with the US pharmaceutical market, through recent employment with US-based consulting firm
Advanced degree in medicine/ life sciences from leading global faculty (Ph.D. preferred)
Consultant level: 3+ years of relevant professional experience
Track record of professional success, with successive stages of advancement/ promotion
Proven Leadership skills (functional, team, client, team, etc.)
Experience in pharma competitive intelligence
Strong knowledge and hands-on competitive intelligence experience in the pharmaceutical industry, including issue monitoring and coverage of industry conferences, primary C.I., CI deep dives, workshops, scenario planning, and synthesis/ insight generation
Experience working on Commercial Strategy or Market Access projects
Ability and willingness to travel

Job Responsibility

Develops key project deliverables, such as discreet pieces of (qualitative, quantitative, financial, pharmaco-economic) research, analysis and synthesis
Using a range of strategic frameworks, conceptualizes complex data into compelling, succinct and actionable insights
Creates, adheres to, manages, project plan and budget, incl. key milestones, delivery timelines, review sessions, with an eye for available capacity and for potential issues and risks
Scopes out team role(s) and successfully delivers on own such role (including for example, project manager, financial/ quant analyst, communications champion)
Manages small team in executing client project(s), addresses performance concerns effectively and early on
Ensures high quality of deliverables, e.g., through four-eye principle, check list or formal quality control process
Conducts project reviews and provides / seeks formal feedback at the close of every project (or at contract renewal for monitoring projects) to ensure key learnings from the project are captured
Interacts with defined client teams in communicating progress, questions / hypotheses / conclusions, in addressing any questions and concerns, and in flagging issues as needed
Ensures client satisfaction throughout the term of the project
Takes on practice leadership role, e.g., related to recruiting, knowledge management, pursuit leadership.

Fulltime

Pharma Quality Specialist Consultant

Hybrid working - our approach is to be in the office or on client site a minimum...

Location

United Kingdom , London

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

Management Consultancy experience highly desirable
A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline)
Typically 8+ years experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation
Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates
Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance
Hands-on experience with supplier qualification, audits, CAPA and compliance management
Experience of RIM and PLM system implementation in regulated environments (highly desirable)
Knowledge of computer system validation and data integrity principles
Excellent problem-solving, communication and stakeholder management skills
QP status is highly desirable but not essential

Job Responsibility

QMS design and process transformation
Leading the design and implementation of GxP-compliant QMS across R&D, manufacturing, clinical and distribution environments
Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10)
Authoring, reviewing and maintaining quality policies, standards, SOPs, forms and controlled documentation, enabling sustainable compliance and operational excellence
Supporting effective change management, embedding best practices through close collaboration with quality, technical and business teams
Computer system validation and data integrity
Leading and advising on computer system validation (CSV) activities within GxP environments
Supporting the development of validation strategies, protocols, test scripts and data integrity controls in line with global regulatory expectations
Supplier quality and audit support
Applying hands-on experience in supplier qualification, evaluation and audit activities (internal and external)

What we offer

Health and lifestyle perks accompanying private healthcare
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

Pharma Quality Specialist Consultant

Hybrid working - our approach is to be in the office or on client site a minimum...

Location

United Kingdom , London

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

Management Consultancy experience highly desirable
A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline)
Typically 8+ years’ experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation
Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates
Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance
Hands‑on experience with supplier qualification, audits, CAPA and compliance management
Experience of RIM and PLM system implementation in regulated environments (highly desirable)
Knowledge of computer system validation and data integrity principles
Excellent problem‑solving, communication and stakeholder management skills

Job Responsibility

QMS design and process transformation
Computer system validation and data integrity
Supplier quality and audit support
Regulatory systems implementation
Regulatory and Qualified Person (QP) support
Client and stakeholder engagement

What we offer

Health and lifestyle perks accompanying private healthcare
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

Pharma Quality Specialist Consultant

Our Life Sciences teams work with leading pharmaceutical, biotechnology and heal...

Location

United Kingdom , London

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

Management Consultancy experience highly desirable
A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline)
Typically 8+ years’ experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation
Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates
Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance
Hands‑on experience with supplier qualification, audits, CAPA and compliance management
Experience of RIM and PLM system implementation in regulated environments (highly desirable)
Knowledge of computer system validation and data integrity principles
Excellent problem‑solving, communication and stakeholder management skills
QP status is highly desirable but not essential

Job Responsibility

QMS design and process transformation
Computer system validation and data integrity
Supplier quality and audit support
Regulatory systems implementation
Regulatory and Qualified Person (QP) support
Client and stakeholder engagement

What we offer

Health and lifestyle perks accompanying private healthcare
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

Pharma Quality Specialist Consultant

We are seeking an experienced Pharma Quality Specialist Consultant to join our L...

Location

United Kingdom , Melbourn

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline)
Typically 8+ years’ experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation
Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates
Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance
Hands‑on experience with supplier qualification, audits, CAPA and compliance management
Excellent problem‑solving, communication and stakeholder management skills

Job Responsibility

QMS design and process transformation
Computer system validation and data integrity
Supplier quality and audit support
Regulatory systems implementation
Regulatory and Qualified Person (QP) support
Client and stakeholder engagement

What we offer

Health and lifestyle perks accompanying private healthcare
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

New

Manager, Health Economics & Outcomes Research (HEOR)

The Manager, Health Economics & Outcomes Research (HEOR) is the primary health e...

Location

United States , Deerfield

Salary:

136000.00 - 187000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelors in Health Economics, Outcomes Research, Epidemiology, or related field
5+ years of HEOR experience in MedTech, Pharma, or consulting, preferably with hospital-based products
Proven experience developing economic models (BIA, CEA)
Demonstrated experience in scientific publication development and evidence communication
Strong ability to interpret outputs from real-world data analyses (e.g., SQL, R, Python-supported workflows)
Up to 30% travel

Job Responsibility

Design and maintain economic models, including budget impact analyses (BIA) and cost-effectiveness analyses (CEA), across the surgical portfolio (e.g., Floseal, Tisseel, Coseal)
Develop frameworks to translate hospital utilization data into total cost of care, efficiency, and product optimization insights
Provide the scientific foundation to support value-based agreements and hospital contracting through economic evidence generation
Define the evidence generation strategy and identify key clinical and economic evidence gaps in the U.S. surgical market
Lead the design of retrospective real-world evidence (RWE) studies and guide analytic execution in partnership with RWD analysts
Conduct literature reviews and meta-analyses to benchmark product performance against competitive technologies
Lead development of peer-reviewed manuscripts, abstracts, and conference submissions (e.g., ISPOR, AORN, surgical congresses)
Develop and maintain compliant scientific exchange tools (Safe Harbor materials) for Medical Science Liaisons and field teams
Lead Medical/Legal/Regulatory (MLR) review processes to ensure all materials meet compliance requirements
Partner with Medical Affairs leadership, RWD analysts, and cross-functional teams to align evidence generation with strategic priorities

What we offer

Medical and dental coverage starting on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP) with ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP) with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

New

Associate Director of Value Creation

Dawn Health is a leading digital health company enabling Life Science partners t...

Location

Denmark , Copenhagen

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

7-10 years experience in either consulting, digital innovation or commercial strategy within start-up, consulting or Big Pharma environments
Excited about solving complex challenges through innovative solutions and then being hyper-focused on tactical execution to deliver the value
Strong ability to leverage large number of insights & quantitative information to dissect highest value opportunities and define priorities
Vast experience in client-facing or matrixed roles utilizing soft influence to drive programs and ensure alignment in complex settings
Determination to continuously find areas of opportunity to improve performance, execution and scale of our solutions to maximize impact and value creation
Exceptional communicator who is able to resolve complexity and always be anchored in common goals & objectives, both externally and internally
Min. Master’s Degree in a relevant field (e.g., Business, Strategy, Engineering or Computer Science)

Job Responsibility

Co-create the value proposition & design of solutions together with our Life Science Partners anchored in measurable outcomes for patients and our partners that can then be taken over by the Delivery teams to execute in highest quality
Own the unlocking of the full potential of each solution through data-driven continuous improvement efforts, facilitating platform-based innovation to further strengthen the solution and its impact as well as identifying opportunities for further scaling of each solution
Be the trusted partner to our Life Science Partners working hand-in-hand with them to assess impact & success of the solutions and formulating and jointly presenting the value story within the partner organization
Represent the customer voice & vision towards the internal organization to ensure our partners` needs are reflected in the product strategy and the delivery of our solutions is done with highest possible quality and consistency leveraging the industry-leading Dawn Health platform

What we offer

The ability to be at the fore-front of digital innovation in healthcare, defining and bringing to life products that impact patient lives at scale
Autonomy, trust, and support within Dawn Health to continuously learn, grown and develop into your full potential in a highly collaborative environment
Ability to work directly with our industry/leading of Life Science Partners who are at the forefront of some of the biggest advancement in medicine and care
Competitive compensation package
Copenhagen’s best view 🌅 and best office espresso machine ☕️

Fulltime

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Pharma Data Science Consultant

Job Description

Job Responsibility

Requirements

What we offer

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