Clinical Project Manager (F/M/X)

Amaris Consulting

Eindhoven

Hybrid

EUR 75,000 - 100,000

Full time

2 days ago
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Benefits offered by this job

International community
Leadership development
Internal Academy
Team events
ESG initiatives
Gym club
Lunch vouchers
Free Spanish classes

Job summary

Amaris Consulting is seeking an experienced Clinical Project Manager to lead multinational clinical studies in a regulated environment. You will coordinate cross-functional teams across Clinical Operations, Medical, Regulatory, Quality and Data Management, ensuring adherence to protocol and GCP.

The role offers exposure to international projects, collaboration with CROs and sites, and opportunities for professional growth. Remote policy allows 2 days of remote work per week.

Qualifications

  • Minimum 5 years of experience in clinical project management within a pharmaceutical, biotech, medical device or CRO environment.
  • Proven experience leading clinical trials and multidisciplinary teams.
  • Strong knowledge of GCP and applicable regulatory standards.
  • Experience managing CROs, clinical sites and external vendors.
  • Fluent English; French and/or additional languages are a plus.

Responsibilities

  • Lead and coordinate clinical projects from study start-up through close-out.
  • Develop and monitor project timelines, budgets, resources and key milestones.
  • Coordinate cross-functional teams including Clinical Operations, Medical, Regulatory Affairs, Quality, Data Management and external partners.
  • Oversee the selection, initiation and performance of clinical sites.
  • Manage relationships with CROs, vendors and other external stakeholders.
  • Ensure clinical activities are conducted in accordance with protocol requirements, GCP and applicable regulatory standards.
  • Monitor project progress, identify risks, issues and dependencies, and implement appropriate mitigation plans.
  • Ensure the quality, completeness and timely delivery of clinical documentation and study deliverables.
  • Prepare and contribute to audits and inspections.
  • Provide regular project updates, status reports and recommendations to key stakeholders and senior management.
  • Contribute to the continuous improvement of clinical project management processes and practices.

Skills

Clinical project management
Team management
GCP knowledge
CRO/vendor coordination
English fluency

Education

Bachelor’s or Master’s in Life Sciences/Pharmacy/Medicine

Tools

Regulatory knowledge

Job description

Join Amaris Consulting and support one of our leading clients in the successful delivery of clinical studies within an international and highly regulated environment.

Your responsibilities
  • Lead and coordinate clinical projects from study start-up through close-out.
  • Develop and monitor project timelines, budgets, resources and key milestones.
  • Coordinate cross-functional teams including Clinical Operations, Medical, Regulatory Affairs, Quality, Data Management and external partners.
  • Oversee the selection, initiation and performance of clinical sites.
  • Manage relationships with CROs, vendors and other external stakeholders.
  • Ensure clinical activities are conducted in accordance with protocol requirements, GCP and applicable regulatory standards.
  • Monitor project progress, identify risks, issues and dependencies, and implement appropriate mitigation plans.
  • Ensure the quality, completeness and timely delivery of clinical documentation and study deliverables.
  • Prepare and contribute to audits and inspections.
  • Provide regular project updates, status reports and recommendations to key stakeholders and senior management.
  • Contribute to the continuous improvement of clinical project management processes and practices.
About you
  • Minimum 5 years of experience in clinical project management within a pharmaceutical, biotech, medical device or CRO environment.
  • Proven experience managing clinical trials and multidisciplinary teams.
  • Good knowledge of GCP and applicable clinical research regulations.
  • Experience working with CROs, clinical sites and external vendors.
  • Experience managing international and/or multicenter clinical studies is a strong advantage.
  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine or a related field.
  • Strong project management, organizational and stakeholder management skills.
  • Ability to manage multiple priorities, anticipate risks and work effectively in a complex environment.
  • Fluent English; French and/or additional languages are a plus.
What we offer
  • An international community bringing together 110+ different nationalities
  • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibility
  • A robust training system with our internal Academy and 250+ available modules
  • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
  • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support.
  • Benefits: access to our gym club, lunch vouchers and free Spanish classes
  • Remote policy: Possibility to work remotely 2 days per week

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

#LI-MR2

Who are we?

Amaris Consulting isan independent technologyconsulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of7,600 people spread across 5 continents and more than 60countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

Job description

Join Amaris Consulting and support one of our leading clients in the successful delivery of clinical studies within an international and highly regulated environment.

Your responsibilities
  • Lead and coordinate clinical projects from study start-up through close-out.
  • Develop and monitor project timelines, budgets, resources and key milestones.
  • Coordinate cross-functional teams including Clinical Operations, Medical, Regulatory Affairs, Quality, Data Management and external partners.
  • Oversee the selection, initiation and performance of clinical sites.
  • Manage relationships with CROs, vendors and other external stakeholders.
  • Ensure clinical activities are conducted in accordance with protocol requirements, GCP and applicable regulatory standards.
  • Monitor project progress, identify risks, issues and dependencies, and implement appropriate mitigation plans.
  • Ensure the quality, completeness and timely delivery of clinical documentation and study deliverables.
  • Prepare and contribute to audits and inspections.
  • Provide regular project updates, status reports and recommendations to key stakeholders and senior management.
  • Contribute to the continuous improvement of clinical project management processes and practices.
About you
  • Minimum 5 years of experience in clinical project management within a pharmaceutical, biotech, medical device or CRO environment.
  • Proven experience managing clinical trials and multidisciplinary teams.
  • Good knowledge of GCP and applicable clinical research regulations.
  • Experience working with CROs, clinical sites and external vendors.
  • Experience managing international and/or multicenter clinical studies is a strong advantage.
  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine or a related field.
  • Strong project management, organizational and stakeholder management skills.
  • Ability to manage multiple priorities, anticipate risks and work effectively in a complex environment.
  • Fluent English; French and/or additional languages are a plus.
What we offer
  • An international community bringing together 110+ different nationalities
  • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibility
  • A robust training system with our internal Academy and 250+ available modules
  • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
  • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support.
  • Benefits: access to our gym club, lunch vouchers and free Spanish classes
  • Remote policy: Possibility to work remotely 2 days per week

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

#LI-MR2

Who are we?

Amaris Consulting isan independent technologyconsulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of7,600 people spread across 5 continents and more than 60countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:

Brief Call: Our process typical starts with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!

Interviews: (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!

Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.

We look forward to meeting you!

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