Pharma Data Science Consultant Job at Amaris Consulting (Tokyo)

Analytics Solutions Lead - Pharma

We’re building a world of health around every individual — shaping a more connec...

Location

United States , New York

Salary:

142140.00 - 284280.00 USD / Year

CVS Health

Expiration Date

April 27, 2026

Requirements

5+ years’ experience in Consulting, Program Management, Business Operations or Strategy experience
3+ years’ experience in analytics consulting or management consulting, delivering project‑based outputs, including executive-level presentations and strategic recommendations
3+ years’ experience with data visualization and manipulation in Excel, plus exposure to BI tools (Tableau, Power BI)
2+ years’ experience working with Data Science or Data Engineering teams, with the ability to translate between technical and business stakeholders to deliver healthcare analytics and insights
2+ years’ experience in program management for complex, multi-stakeholder initiatives, including internal coordination and problem-solving across enterprise teams
2+ years’ experience building PowerPoint presentations with an emphasis on executive leaders and stakeholders
1+ year experience in or with the healthcare industry, preferably in pharmaceutical or life sciences, with exposure to commercial, clinical, or market access analytics
Bachelor’s degree, preferably in STEM field (e.g., Science, Technology, Engineering, Mathematics) required

Job Responsibility

Translate business needs into clear, actionable data science requirements
Manage data science pods to implement analytical models tailored to pharmaceutical customer needs, leveraging advanced methodologies (e.g., predictive modeling, machine learning) where appropriate
Apply strong analytical capabilities to translate modeling outputs into client‑ready analyses and deliverables, with deep proficiency in Microsoft Excel and familiarity with BI/visualization tools (e.g., Power BI, Tableau)
Manage cross-functional program delivery by coordinating internal CVS Health stakeholders to assess feasibility of existing capabilities and integrate them into new customer-facing analytics solutions
Draft, refine, deliver, and communicate analytical stories to internal and external executive audiences
Partner with Product Management to relay key customer insights and inform broader product‑building initiatives, influencing roadmap prioritization through evidence-based recommendations
Scope work plans, build delivery timelines, and plan resources to execute analytical consulting engagements
Identify project opportunities based on data and analytics discovery and raise them effectively to business partners
Work cross‑functionally with product partners to identify opportunities to speed up and standardize analytics reporting outcomes
Demonstrate and reinforce best practices in client and business communication

What we offer

Affordable medical plan options
401(k) plan (including matching company contributions)
Employee stock purchase plan
No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching
Paid time off
Flexible work schedules
Family leave
Dependent care resources
Colleague assistance programs
Tuition assistance

Fulltime

Vaf 422 consultant

Location

United States

Salary:

85000.00 - 105000.00 USD / Year

Product Life Group

Expiration Date

Until further notice

Requirements

Bachelor or higher
0-2 years experience in BSI
2-3 years experience in life science domain (specifically within the clinical space)
Familiarity with clinical trial processes in pharma, biotech, or CRO settings
Basic understanding of Clinical Trial Management Systems (CTMS), preferably BSI CTMS
Experience working with structured data, reports, or system based documentation
Comfort with IT systems, troubleshooting, and end-user support
Exposure to ICH-GCP or other regulatory frameworks related to clinical trials

Job Responsibility

Assist with BSI CTMS system setup and configuration under senior consultant guidance
Support system testing: develop test scripts, execute test cases, and log results
Help prepare training materials, user documentation, and quick reference guides
Provide first-level troubleshooting and user support for CTMS-related issues
Contribute to data migration, quality checks, and validation activities
Document requirements, workflows, and meeting notes during client interactions
Learn and apply clinical operations standards and regulatory requirements (e.g., ICH-GCP)
Participate in client workshops and training sessions as a support resource

Fulltime

Digital consultant

Location

United States

Salary:

85000.00 - 105000.00 USD / Year

Product Life Group

Expiration Date

Until further notice

Requirements

Bachelor or higher within pharma, microbiology, chemistry, or IT
3-5 Years of experience
Familiarity with pharmaceutical, biotech, or life sciences laboratory processes and workflows
Prior internship, co-op, or project experience in pharmaceutical/biotech IT systems
Basic understanding of Laboratory Information Management Systems (LIMS)
Experience with data entry, reporting, or system-based documentation in a regulated environment
Comfort with IT systems, troubleshooting, and user support in a lab or business setting
Exposure to GxP, FDA 21 CFR Part 11, or other regulatory requirements in life sciences

Job Responsibility

Assist with LabVantage system configuration under guidance from senior consultants
Support testing activities, including writing test cases, executing scripts, and documenting results
Help prepare user documentation, training materials, and job aids for client teams
Provide first-line troubleshooting and issue triage for LabVantage users
Participate in data migration activities, such as data preparation, validation, and cleanup
Collaborate with business users to gather requirements and document workflows
Maintain project documentation, meeting notes, and status updates
Learn and apply relevant regulatory standards (e.g., GxP, Part 11) in daily work

Partner

Location

Japan , 東京23区,大阪, 東京都

Salary:

12000000.00 - 50000000.00 JPY / Year

Randstad

Expiration Date

January 19, 2027

Requirements

Bachelor's degree with an emphasis in Business or Life Sciences
MBA or Advanced Degree is highly desirable
15+ years’ experience in life science, pharma or healthcare industry management consulting
Demonstrated experience with driving revenue within existing clients and in developing new prospects at the "C" level of Pharmaceutical, Life Sciences, Healthcare or Medical Device companies
Prior experience in Analytics, Big Data, Cloud, Digital Asset Management, Master Data Management and Data Warehousing etc
Demonstrated experience of developing new prospects, driving revenue, and delivering high quality projects and services within budget
Characteristics of a forward thinker and self-starter that thrives on new challenges and adapts quickly to learning new knowledge
Possess executive-level presence and communication skills, with native-level proficiency in both English and Japanese being essential

Job Responsibility

Lead large scale client business development and technology delivery engagements for the clients primarily in the Life Sciences Industry - Pharmaceutical and/or healthcare sector
Shape digital transformation programs and build digital custom solutions (portals, apps etc) powered by data and insights
Actively develop trusted advisor relationships with client executives
Lead technology and cross-functional teams to deliver high quality engagements within timeline and budget
Collaborate closely with other our team members to drive overall Digital & Technology space growth
Build internal connections with the our Business Technology group and represent client's needs
Play an active role in building the space, its talent pool, and growing and mentoring team members
Stay abreast of current business and industry trends relevant to the client's business
Foster an innovation driven culture to design futuristic offerings within Technology space for the region
Effectively lead these offerings into selling collaterals and partner with client service teams in selling process

What we offer

労災保険
日曜日,土曜日,祝日

Fulltime

New

Solutions Engineer, Life Sciences

At Domino, we build software that helps the largest, AI-driven organizations bui...

Location

United States

Salary:

200000.00 - 250000.00 USD / Year

Domino Data Lab

Expiration Date

Until further notice

Requirements

A technical background in life sciences - you will have worked inside a pharma, biotech, CRO, genomics, or medical device organization doing code-first analytical or scientific work. You understand what it actually feels like to build and run things in that environment.
Working knowledge of at least one life sciences domain - drug discovery, clinical development, computational biology, manufacturing/QC, or regulatory data management. Credible in front of scientific stakeholders without needing to be a domain expert.
Platform or tooling ownership experience - ideally you've built, operated, or meaningfully contributed to an internal platform or shared scientific computing environment. You've influenced or helped shape how that platform served its users, even without a formal product owner title.
Experience in a solutions engineering, pre-sales, or customer-facing technical role - or equivalent internal/consulting work where the job was diagnosing technical problems and helping others solve them, not just executing defined tasks.
You've led or contributed to technical evaluations, pilots, or proof-of-concepts - whether at a vendor, internally, or as a consultant - that drove meaningful adoption or investment decisions.
Demonstrated ability to build: you've written production or near-production code to solve a real scientific or operational problem. Experience creating internal tools, pipelines, or applications for scientific teams is a strong signal.
Proficiency in Python and/or R
hands-on experience with the data science and ML tools used in life sciences technical work. Familiarity with how models get built, validated, and moved toward production in a regulated context is a plus.

Job Responsibility

Engage deeply with the technical problems customers are trying to solve.
Design and run hands-on proof-of-concept projects tailored to each customer's environment.
Work with account executives to design architectures that address life sciences-specific requirements around data governance, reproducibility, and validation (e.g., 21 CFR Part 11, GxP environments).
Proactively identify novel use cases within life sciences customers where Domino could create meaningful value.
Build and maintain reusable technical environments and assets that make future customer engagements faster and more substantive.
Partner with Customer Success and Solutions Architects to make sure customers who complete a POC are set up to succeed in production.
Build custom prototypes and applications on top of Domino for customers.

What we offer

equity
company bonus or sales commissions/bonuses
401(k) plan
medical, dental, and vision benefits
wellness stipends

Fulltime

Life Sciences Strategy Lead

Tandem’s Life Sciences team partners with the world’s leading biopharma companie...

Location

United States , New York

Salary:

170000.00 - 250000.00 USD / Year

Tandem

Expiration Date

Until further notice

Requirements

4–10 years in client strategy, delivery operations, partnerships, or customer success—ideally in complex, multi-stakeholder environments
Background in life sciences consulting, data platforms, digital health, or pharma-adjacent strategy roles
Executive presence and fluency — able to engage senior leaders across functions and drive alignment in ambiguous environments
Comfort working with data and technical teams (at minimum the role requires learning SQL and low-code tools)
Strong written and verbal communication
Track record of moving quickly, finding shortcuts, and going to unreasonable lengths to deliver on goals
High NPS with your former teammates

Job Responsibility

Own the post-sale success of strategic biopharma accounts—including onboarding, pilot execution, performance tracking, and client reporting
Act as Tandem’s day-to-day lead across multiple client teams — including commercial, field, access, and data stakeholders
Collaborate closely with our product, engineering, data, and delivery teams to coordinate execution and ensure consistent impact for clients
Drive retention and expansion within accounts by delivering tangible outcomes, sharing insights, and building trust across functions
Design scalable processes for managing multi-workstream accounts with 7–8 figure contract value and help build our client success function as we grow
Explore, evaluate, and execute on new opportunities for the company, including strategic partnerships and new products and services
Work closely with the rest of our team and CEO to make business decisions as we balance speed of growth and long-term profitability

What we offer

Fully covered medical, vision, and dental insurance
Memberships for One Medical, Talkspace, Teladoc, and Kindbody
Unlimited paid time off (PTO) and 16 weeks of parental leave
401K plan setup, FSA option, commuter benefits, and DashPass
Lunch at the office every day and Dinner at the office after 7 pm
Offers Equity

Fulltime

Commercialization Lead

As Commercial Lead on our team, you will drive new business for Tandem in life s...

Location

United States , New York

Salary:

250000.00 - 350000.00 USD / Year

Tandem

Expiration Date

Until further notice

Requirements

8–16 years of experience in strategic partnerships, commercialization, or product-driven BD in complex, multi-stakeholder environments
Background in life sciences consulting, data platforms, digital health, or pharma-adjacent strategy roles
Executive presence and fluency — able to engage senior leaders across functions and drive alignment in ambiguous environments
Technical background and/or experience working with complex data (at minimum the role requires learning SQL and low-code tools)
Strong written and verbal communication that allows you to be an effective participant in both internal debates and external relationships
Track record of moving quickly, finding shortcuts, and going to unreasonable lengths to deliver on goals
High NPS with your former teammates

Job Responsibility

Deeply understand the goals and needs of biopharma companies and serve as a strategic partner to them, bringing credibility, insight, and creativity to every engagement
Own revenue targets and lead the end-to-end lifecycle of new client partnerships — from discovery and scoping through contracting, delivery, and expansion
Design pricing strategies and deal structures that reflect platform value and set up repeatable, scalable commercial models
Collaborate with product, data, and delivery teams to shape our data and product offerings and ensure successful delivery
Build repeatable sales infrastructure and eventually lead a team of generalist BD and client-facing operators
Explore, evaluate, and execute on new opportunities for the company, including strategic partnerships and new products and services
Work closely with the rest of our team and CEO to make business decisions as we balance speed of growth and long-term profitability

What we offer

Fully covered medical, vision, and dental insurance
Memberships for One Medical, Talkspace, Teladoc, and Kindbody
Unlimited paid time off (PTO) and 16 weeks of parental leave
401K plan setup, FSA option, commuter benefits, and DashPass
Lunch at the office every day and Dinner at the office after 7 pm
Offers Equity
Competitive compensation with meaningful equity

Fulltime

Non-Pharma Global Regulatory Affairs Manager

The Global Regulatory Sciences-Legacy Products-Non-Pharma Manager manages regula...

Location

Italy , Bologna; Milano; Pomezia

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Proven experience in Regulatory Affairs within the pharmaceutical or life sciences industry, preferably within the food supplements, medical devices, and cosmetics sectors
Hands-on experience with regulatory submission processes, especially within EU and/or RoW markets or similar relevant experiences
Demonstrated ability to coordinate projects or deliverables with complexity and limited supervision
Advanced degree in Life Sciences, Pharmacy, Chemistry, or a related field
Good knowledge of global regulatory frameworks including EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
Strong organizational skills, attention to detail, and ability to manage priorities
Collaborative mindset and effective communication with team members and stakeholders
Ability to operate independently on clearly defined assignments
Proficiency in Microsoft Office Suite and regulatory submission/document management tools
Fluent in English, both written and spoken

Job Responsibility

Accountable for providing the necessary regulatory inputs in a cross-functional team for the development of new projects
Accountable for the execution and implementation of global regulatory strategies by managing day-to-day activities for assigned products
Manage multiple regulatory workstreams independently, including authoring, reviewing and coordinating documentation for regulatory submissions such as variations, renewals and geo-expansions
Provide and review regulatory assessments for change controls and product updates
Responsible for the preparation, review and collection of documentation for submission and maintenance of Technical File and PTD for the project assigned
Provide critical review of documentation supporting regulatory applications
Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
Contribute to the preparation and presentation of regulatory project updates in internal meetings and governance committees
Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
Support other relevant assignments as directed by supervisor

What we offer

Competitive salary
Comprehensive benefits
Extensive opportunities for professional growth and development

Pharma Data Science Consultant

Amaris Consulting

Location:
Japan , Tokyo

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 27, 2026

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