Clinical Project Manager Job at AB SCIENCE (Paris)

Intern, project manager, clinical development

The BioMarin Summer Internship Program will enable students to gain valuable exp...

Location

United States , San Rafael

Salary:

24.00 - 27.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

In progress bachelor’s degree in health or life sciences, including chemistry, molecular biology, or similar
Must be available to work full-time, 40 hours a week
Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles

Job Responsibility

Work closely with the Clinical Development PM to propose a new structure and content plan for the PMO SharePoint site
Engage with representatives from each PMO branch to understand their roles and contributions to drug development
Gather and organize key resources and documentation to improve accessibility and transparency
Tracking project and program timelines, drive action item completion, and document decision making for CDTs
Scheduling clinically focused meetings, generate the agenda and facilitate the meeting (in collaboration with the team lead), and document/distribute minutes and action items
Identifying opportunities for standardization or process efficiencies based on cross-functional insights
Attend cross-functional team meetings and Production Integration Management Team (PRIME) team meetings to develop an understanding of clinical development

What we offer

Paid hourly wage, paid company holidays, and sick time
Apply skills and knowledge learned in the classroom to on-the-job experiences
Comprehensive, value-added project(s)
Develop skills specific to your major
Opportunities for professional development by building relationships and learning about other parts of the business
Participate in company all hands meetings, monthly community lunches
Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
Access to Employee Resource Groups

Fulltime

Senior Manager of Informatics - Project Management

The Epic Implementation Project Manager assists the Lead Director with informati...

Location

United States , Work at Home

Salary:

130295.00 - 260590.00 USD / Year

CVS Health

Expiration Date

February 09, 2026

Requirements

Minimum of five (5) years of related experience is required
Two or more Epic Certifications: EpicCare Ambulatory, Healthy Planet, Beacon, Willow, Prelude, Cadence, Resolute Professional Billing, HIM (Health Information Management), MyChart, Beaker, Welcome Kiosk, Rover, Haiku, EpicCare Link, Caboodle, SlicerDicer, Bridges, Reporting Workbench, Orders
Deep expertise in IT project management
Risk mitigation and change adoption
Proven ability to deliver complex healthcare technology projects on time and within scope

Job Responsibility

Strategic Project Management: Translate strategic goals into actionable project plans
Set and manage milestones
Maintain project timelines using tools (e.g., Smartsheet, MS Project, MS Excel, MS Visio)
Risk & Issue Management: Develop and maintain risk logs
Create escalation pathways
Support development and maintain tracking tools in MS Excel for financial assessment and forecasting
Cross-Functional Coordination: Ensure alignment across clinical, technical, and operational workgroups
Lead effective cross-functional meetings
Communication, Relationship Development & Reporting: Deliver executive-level reporting
Develop and maintain relationships with key stakeholders

What we offer

Affordable medical plan options
401(k) plan with matching company contributions
Employee stock purchase plan
No-cost wellness screenings
Tobacco cessation and weight management programs
Confidential counseling and financial coaching
Paid time off
Flexible work schedules
Family leave
Dependent care resources

Fulltime

Analyst, Clinical Data Management, Clinical Informatics-Ambulatory

As part of the Epic team, you will be expected to be proficient in all critical ...

Location

United States , Work From Home

Salary:

83430.00 - 222480.00 USD / Year

CVS Health

Expiration Date

March 02, 2026

Requirements

Minimum of five (5) years of related experience is required
Two or more Epic Certifications: EpicCare Ambulatory, Healthy Planet, Beacon, Willow, Prelude, Cadence, Resolute Professional Billing, HIM (Health Information Management), MyChart, Beaker, Welcome Kiosk, Rover, Haiku, EpicCare Link, Caboodle, SlicerDicer, Bridges, Reporting Workbench, Orders
Bachelor's degree is required or equivalent experience
Strong experience configuring, designing, and supporting an Epic solution
Previous application configuration experience
Knowledge of Ambulatory workflows and quality and safety initiatives
Experience in test planning & execution, test case development, and meeting project quality requirements
Experience working on large projects, strong knowledge of clinical applications and understanding of the healthcare IT industry
Understanding of configurable applications and monitoring practices
Analytical, problem resolution and interpersonal skills

Job Responsibility

Design and develop and facilitate deployment of the quality and safety initiatives
Oversee build and maintenance of Epic environments, related in particular to Medical Affairs safety efforts
Facilitate communication and problem solving sessions to identify, scope and plan for safety mitigation plans
Maintain comprehensive documentation of materials and methodologies, user guides, and support resources
Create and fulfill EHR use cases, identify business and functional requirements and working closely with IT resources to translate requirements and workflows to technical specifications
Lead documentation efforts for discovery and implementation
Ensure requirements and future state workflows are clearly defined
Support development of Quality and Safety Governance and guidance group supporting both Oak Street Health and all CVS business units
Work with across the CVS enterprise to identify tasks and associated business units impacted by quality & safety efforts
Support execution of vendor upgrades, system changes and environment maintenance procedures

What we offer

Affordable medical plan options
401(k) plan with matching company contributions
Employee stock purchase plan
No-cost wellness screenings
Tobacco cessation and weight management programs
Confidential counseling and financial coaching
Paid time off
Flexible work schedules
Family leave
Dependent care resources

Fulltime

Clinical Project Associate

An ideal candidate for our Clinical Project Associate position is an individual ...

Location

Salary:

23.00 - 28.00 USD / Hour

canfield scientific

Expiration Date

Until further notice

Requirements

Associate degree or at least 1 year work experience
Proficiency in Microsoft Office
Strong time management, problem-solving, and organizational skills
Ability to adjust to shifting priorities and meet timelines
Detail oriented, flexible, and works well within a team environment

Job Responsibility

Provide project management and operational support to designated clinical project team ensuring that quality, timelines, and project specifications are met
Manage study documentation ensuring accuracy within the documentation while aiding in the preparation of supply shipments to study sites
Setup, maintain, and update databases and assist with data query resolution
Perform quality control checks to ensure the integrity of data and may support initiation phase of project
Communicate with study sites by fielding, answering, and directing questions to obtain information and direct to corresponding personnel

What we offer

Paid days off
Medical, dental, and vision insurance
May be eligible for a discretionary bonus
401(k) plan with employer match (currently set at 50%)

Fulltime

Manager, Clinical Operations, International

Cabaletta is seeking a Manager/Sr Manager, Clinical Operations, International. R...

Location

Germany; Switzerland

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Bachelor’s Degree or advanced degree in life sciences or related field
Minimum 4 years of clinical trial management experience including management of study resources, vendors, budgets, supplies, critical path activities, and risk management, within Biotech or pharmaceutical industry or equivalent by experience
Cell therapy experience preferred and/or focus complex therapies
Fluency in English
working proficiency in additional European languages a plus
Experience with early phase, complex trials
Experience managing Contract Research Organizations and other external vendors
Good understanding of European regulatory requirements (EMA, MHRA, etc)
Working knowledge of GCP/ ICH regulatory guidelines
Extensive knowledge of standard industry practices related to study start-up, site management and monitoring, document management, and clinical supply management

Job Responsibility

Provide day-to-day clinical project management oversight of the full range of clinical operations activities associated with clinical trial conduct from protocol development, feasibility/capability assessments, initiation, execution, control, and closure
Perform hands-on activities not outsourced to vendors, as needed
Author study documents and plans such as ICF and study specific plans
Provide input and review of site training materials
Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate
Proactively identify risks and lead team members to mitigate risks in a timely fashion
Develop and maintain positive relationships, both internal and external to project, including site personnel (KOLs, PIs, Study Coordinators)
Select and manage vendors
Perform and document study-level Sponsor Oversight of outsourced clinical activities
Execute clinical operations country submission tasks and documents: Review submission pack, coordinate country-specific ethics RFIs, review and update site-specific consent forms

What we offer

health and retirement
PTO
stock option plans

Project Manager

A well-established consultancy based in Newcastle is currently looking for a Pro...

Location

United Kingdom , Newcastle upon Tyne

Salary:

45000.00 - 55000.00 GBP / Year

Brandon James

Expiration Date

Until further notice

Requirements

Proven experience working as a Project Manager in a consultancy or client-side setting
Demonstrable experience delivering healthcare projects (NHS or private sector)
Degree in Project Management, Construction Management, or a related field
Ideally chartered or working towards MRICS / MAPM / MCIOB
Strong understanding of NEC and/or JCT contracts
Full UK driving licence preferred

Job Responsibility

Leading multiple healthcare-related projects from feasibility through to completion
Managing stakeholder relationships
Producing project documentation
Reporting progress
Coordinating with design, cost, and engineering teams to meet client objectives
Ensuring projects comply with healthcare regulations and clinical requirements
Working on live hospital environments

What we offer

Pension and private healthcare
APC or Chartership support if required
Genuine progression opportunities
Established client base with repeat healthcare work

Fulltime

IT Technical Project Manager

We are seeking a highly skilled and motivated IT Technical Project Manager to jo...

Location

United States , York, Maine

Salary:

99000.00 - 119000.00 USD / Year

Altera Digital Health Inc. UK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in computer science, Information Technology, Healthcare Management, or related field
PMP, Scrum Master, or other project management certifications preferred
Minimum 3–5 years of experience in IT project management, with at least 2 years in a healthcare setting
Strong technical background with a solid understanding of healthcare IT systems (EMR/EHR, PACS, networking, etc.)
Proven experience managing multiple, complex projects simultaneously
Experience with hospital workflows, clinical systems, and healthcare regulations (HIPAA, HITECH) is a plus
Excellent communication and interpersonal skills
Strong organizational skills with the ability to manage competing priorities and tight deadlines
Familiarity with project management tools (e.g., Microsoft Project, Jira, Asana) and methodologies (Agile, Waterfall)
Ability to problem-solve and think critically in a fast-paced environment

Job Responsibility

Oversee the full project lifecycle for IT initiatives, including planning, executing, monitoring, and closing projects
Lead cross-functional teams of IT professionals, clinical staff, and vendors
Serve as the primary point of contact for project stakeholders
Identify, assess, and mitigate project risks and issues
Apply technical knowledge to ensure that the solutions being implemented align with hospital infrastructure, security, and regulatory requirements
Continuously evaluate and improve project management processes, tools, and methodologies
Develop and manage project budgets, including resource allocation and vendor contracts
Ensure that all IT projects meet or exceed quality standards
Maintain detailed project documentation, including project plans, schedules, and post-implementation reviews

What we offer

Competitive salary based on experience
Comprehensive benefits package (health, dental, vision, 401k)
Generous paid time off (Flex PTO) and holiday schedule
Professional development opportunities and certifications
Collaborative work environment focused on patient care and technology innovation

Fulltime

Senior Clinical Trial Manager

The Senior Clinical Trial Manager (Sr. CTM) will manage the planning, execution,...

Location

United States , Waltham

Salary:

136000.00 - 170000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

8+ years of clinical trial experience, including direct management of CROs and vendors
Proven ability to lead cross-functional study teams and drive clinical programs forward independently
Deep understanding of GCP, ICH guidelines, and regulatory frameworks relevant to global clinical trial management
Strong problem-solving, organizational, and analytical skills with the ability to anticipate challenges and implement solutions
Excellent written and verbal communication skills, including stakeholder presentations and vendor negotiations
Ability to manage multiple priorities in a fast-paced environment and lead initiatives with minimal oversight
Proficient in Microsoft Office Suite, and working knowledge of project management tools (e.g., MS Project, Smartsheet)
Must be able to travel as needed
Bachelor’s degree in life sciences or a related field

Job Responsibility

Serve as the primary operational lead for assigned clinical trials
accountable for end-to-end trial execution, including oversight of CROs and vendors, from study start-up through close-out
Lead cross-functional trial teams to ensure alignment on timelines, deliverables, risk mitigation, and study objectives
Independently manage key trial activities, such as protocol development, site selection, study conduct, monitoring, data review, and database lock
Oversee and review key clinical trial documents (e.g., informed consent forms, investigator brochures, monitoring plans), ensuring quality and regulatory compliance
Monitor CRO performance to ensure adherence to study plans, timelines, budgets, and quality expectations
escalate and resolve issues proactively
Lead development and review of study plans and vendor SOPs
ensure appropriate documentation and risk mitigation strategies are in place
Ensure timely data query resolution, review of protocol deviations, and follow-through on site-related corrective actions

What we offer

Comprehensive health benefits and tax-advantaged savings accounts
Flexible time off, 13 paid holidays, and a companywide year-end shutdown
Monthly wellness stipend
Generous 401(k) match
Disability and life insurance

Fulltime

Clinical Project Manager

AB SCIENCE

Location:
France , Paris

Category:
Research and Development

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 01, 2025

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