Senior Digital Life Science Consultant Job at Product Life Group (Milan)

Senior Consultant- Life Science Consulting-Italy

LifeBee, is a ProductLife Group Company and leading international strategic and ...

Location

Italy , Firenze, Italy, Milano, Rome

Salary:

Not provided

Product Life Group

Expiration Date

Until further notice

Requirements

STEM degree (i.e., computer science, computer engineering, biomedical engineering, statistics, mathematics, physics)
2 or more years’ experience in Consultant role familiarity with Life Science Software solution, regulations and guidelines good knowledge of individual productivity tool (MS Office)
Knowledge of industry sector guidelines (ISPE, GAMP5, GMP, GxP) and regulations which may apply to Life Science regulated processes
Familiarity with Life Science Software solution, regulations and guidelines good knowledge of individual productivity tool (MS Office)

Job Responsibility

Advising customers, on the most suitable solutions to their needs
Implementing, customizing, integrating, test and validation of market-leading and cutting-edge software applications for Life Sciences
Planning and executing projects streams, drafting specification, tests and validation technical documentation
Enhancing collaboration with local and global software vendors
Providing qualified technical and functional support and training
Aiding customers in technical validation activities

Fulltime

Senior Commercial Consultant - Life Sciences

We’re looking for experienced professionals to join our dynamic team, spanning C...

Location

United States , Boston; New York

Salary:

124100.00 - 226200.00 USD / Year

PA Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Business, Biology, Pharmacology, or a related field
3+ years of Consulting experience in the biotechnology, pharmaceutical, or life sciences with expertise in at least one of the following: Brand strategy, Commercial, Pricing and market access, Commercial operations model transformation, Digital campaign management strategy
Strong commercial strategy with a focus on the US market dynamics, including knowledge of IRA, Medicare, Medicaid
Proven experience in primary research, conducting interviews, and managing quantitative surveys within the life sciences industry
Expertise in pharmaceutical datasets (e.g., pricing, prescription, claims databases) and proficiency in Excel
A demonstrated ability to lead teams, manage client relationships, and deliver strategic insights that drive value

Job Responsibility

Lead and support client engagement teams, delivering high-quality solutions across commercial strategy, product launch, marketing, and business transformation for life sciences clients
Manage and execute key workstreams in large-scale client projects, ensuring project milestones and outcomes are met
Provide strategic insights and solutions in areas including commercial strategy, product launch, marketing, and analytics
Contribute to fostering a collaborative, innovative, and inclusive work environment, mentoring and developing junior team members
Build and nurture long-term client relationships, expanding networks across PA Consulting and client organizations
Stay current with industry trends, emerging technologies, and innovations in life sciences, commercial operations, and analytics

What we offer

Group medical insurance
Health Savings Account with company match
Teladoc and informed Nurse line resources
Long term care plan
Group dental insurance
Vision plan
401(k) Savings Plan with company profit sharing contribution
Commuter and Parking tax-savings benefit
15 days paid vacation days with the opportunity to buy five additional days
10 paid Holidays plus 10 paid sick days

Fulltime

Senior Commercial Consultant - Life Sciences

We’re looking for experienced professionals to join our dynamic team, spanning C...

Location

United States of America , Boston; New York City

Salary:

124100.00 - 226200.00 USD / Year

PA Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Business, Biology, Pharmacology, or a related field
3+ years of Consulting experience in the biotechnology, pharmaceutical, or life sciences with expertise in at least one of the following: Brand strategy
Commercial
Pricing and market access
Commercial operations model transformation
Digital campaign management strategy
Strong commercial strategy with a focus on the US market dynamics, including knowledge of IRA, Medicare, Medicaid
Proven experience in primary research, conducting interviews, and managing quantitative surveys within the life sciences industry
Expertise in pharmaceutical datasets (e.g., pricing, prescription, claims databases) and proficiency in Excel
A demonstrated ability to lead teams, manage client relationships, and deliver strategic insights that drive value

Job Responsibility

Lead and support client engagement teams, delivering high-quality solutions across commercial strategy, product launch, marketing, and business transformation for life sciences clients
Manage and execute key workstreams in large-scale client projects, ensuring project milestones and outcomes are met
Provide strategic insights and solutions in areas including commercial strategy, product launch, marketing, and analytics
Contribute to fostering a collaborative, innovative, and inclusive work environment, mentoring and developing junior team members
Build and nurture long-term client relationships, expanding networks across PA Consulting and client organizations
Stay current with industry trends, emerging technologies, and innovations in life sciences, commercial operations, and analytics

What we offer

Group medical insurance
Health Savings Account with company match
Teladoc and informed Nurse line resources
Long term care plan
Group dental insurance
Vision plan
401(k) Savings Plan with company profit sharing contribution
Commuter and Parking tax-savings benefit
15 days paid vacation days with the opportunity to buy five additional days
10 paid Holidays plus 10 paid sick days

Fulltime

Senior Consultant - Regulatory Affairs

LifeBee, is a ProductLife Group Company and leading international strategic and ...

Location

Italy , Firenze; Milano; Rome

Salary:

Not provided

Product Life Group

Expiration Date

Until further notice

Requirements

STEM degree (i.e., computer science, computer engineering, biomedical engineering, statistics, mathematics, physics)
2 or more years’ experience in Consultant role familiarity with Life Science Software solution, regulations and guidelines good knowledge of individual productivity tool (MS Office)
Knowledge of Life Sciences Software solutions, regulations and guidelines
Analytical and problem solving approach
Fluency in Italian and English is required.

Job Responsibility

Advising customers, on the most suitable solutions to their needs
Implementing, customizing, integrating, test and validation of market-leading and cutting-edge software applications for Life Sciences
Planning and executing projects streams, drafting specification, tests and validation technical documentation
Enhancing collaboration with local and global software vendors
Providing qualified technical and functional support and training
Aiding customers in technical validation activities

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

Senior Conference Producer, Life Sciences

We are seeking a highly motivated and experienced conference producer to join ou...

Location

United Kingdom

Salary:

Not provided

Kisaco Research

Expiration Date

Until further notice

Requirements

Graduated/graduating with a 2:1 or above
Minimum of 1-2 years’ experience in B2B Events
Analytical, commercially minded and dynamic
Ability to articulate and present complex information in an engaging and simple way
Great communication skills both written and verbal
English Fluency
Right to work in the UK
Ability to write crisp engaging copy for a technical/scientific audiences
Highly organised, methodical, and process-driven
High level of attention to detail

Job Responsibility

Undertake research and analysis to determine the commercial viability of conferences within the portfolio, scaling existing products and launching new events
Collaborate with industry experts and thought leaders to develop engaging agendas
Develop ideas for creative digital content to support commercial campaign
Identify and recruit high-profile speakers and moderators
Work with the marketing lead to identify appropriate marketing channels and to ensure that the correct market segments are reached
Collaborate with the marketing team to develop and implement effective promotion strategies
Identify potential sponsors and work with the Commercial Partnerships Manager to agree on the sales plan for your event campaign
Work with speakers, consultants, journalists, and other information providers to source and repurpose materials for content marketing
Build the identity and create buzz around each event with the marketer in the build-up to and during a conference through social media including LinkedIn
Develop and manage budgets for each conference, ensuring financial goals are met

What we offer

£100 personal development budget
£200 personal wellness budget
Hybrid working (3 days in office, 2 from home)
Access to the best Tech – including Gong and Sales Navigator
25 days of annual leave (in addition to bank holidays)
An additional day off for your birthday each year
1 extra day of annual leave per year up to 30 days total
Regular social and charitable events
Annual Summer & Christmas parties

Fulltime

Mid-to-Senior Level Project Manager - Healthcare & Life Sciences

This role plays a critical part in ensuring client work is delivered predictably...

Location

United States , Raleigh

Salary:

Not provided

Carimus

Expiration Date

Until further notice

Requirements

8+ years of project management experience in client-facing environments, including work in Healthcare, Life Sciences, or similarly regulated industries
Proven ability to own end-to-end delivery across cross-functional teams
Working knowledge of planning, estimation, and resourcing for technical or digital work in regulated settings
Experience managing scope, timelines, and budgets with accountability for outcomes, including navigating compliance- or approval-driven constraints
Excellent organizational skills including the ability to manage multiple projects at once
Excellent written and verbal communication skills
Able to demonstrate confidence when working with both technical and non-technical stakeholders
Passion for superb customer experience
Bachelor’s degree in a related field, or equivalent professional experience
Solid analytical and problem solving skills and strong attention to details, particularly in delivery, risk, and compliance sensitive work

Job Responsibility

Manage 4–6 active projects with healthcare and life sciences clients, with the goal of increasing account footprint through monthly recurring revenue and delivery
Own end-to-end delivery for multiple client accounts, balancing scope, resourcing, delivery quality, and regulatory considerations
Align clients, creative teams, and engineering around clear scope, timelines, resourcing decisions, and delivery constraints common in regulated environments
Partner closely with engineering to plan work, estimate effort, and ensure teams are appropriately staffed and aligned, accounting for compliance, privacy, and approval cycles
Plan, organize, monitor, and control projects using appropriate tools and techniques to ensure the project team adheres to project requirements and regulatory expectations
Assist in the definition of project scope and objectives, involving all stakeholders, including clinical, regulatory, or compliance partners and ensuring technical feasibility
Develop and maintain a project plan outlining tasks, milestones, status, costs, and resource allocation, factoring in review, approval, and dependency timelines
Monitor scope creep and convert into billable change requests when possible, particularly as requirements evolve due to compliance or regulatory needs
Accurately book and forecast required staff across creative and engineering
monitor utilization, burn, and delivery health in highly regulated client environments

Fulltime

Senior Manager, Patient Safety

The Senior Manager, Medical Device end to end Management is a leadership role re...

Location

India , Hyderabad

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in Patient Safety Services
demonstrated success in clinical, medical, or scientific domains
People management capabilities with experience leading teams
Experience in client relationship management
Understanding of pharmacovigilance operations, clinical research methodologies, and regulatory frameworks
Clinical experience with progressive responsibilities
Strong clinical, regulatory, and medical Patient Safety Services knowledge
Good understanding of ICH, CIOMS, GVP, and pharmacovigilance requirements
Familiarity with automation/AI in pharmacovigilance
Adaptable mindset with enthusiasm for learning

Job Responsibility

Lead the complete lifecycle of medical device complaint handling and post-market surveillance
Oversee FDA MDR reporting including 5-Day, 30-Day, and Supplemental Reports
Ensure high-quality investigations, root cause analysis, and CAPA linkage
Maintain compliance with 21 CFR 803, 820, ISO 13485, and internal QMS standards
Partner with Regulatory, Quality, R&D, and Manufacturing teams to manage product performance and patient safety insights
Support FDA inspections and internal/external audits
Manage and mentor a high-performing complaint operations team
Delegate work to Patient Safety staff according to allocated budget/hours
Coordinate with Solutions Consultant and/or regional Head of Safety Services as appropriate to assign resources to the project, and to assess staffing needs for current and future activities
Conduct interviews for recruitment of new personnel as necessary

Fulltime

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Senior Digital Life Science Consultant

Job Description

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