Project Manager

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Hiring Remotely in Amsterdam, NLD
In-Office or Remote
Mid level
Software
The Role
Manage clinical research study delivery from planning through completion, ensuring milestones, data quality, risk management, information security, and customer satisfaction. Serve as a trusted consultant to clients, translate clinical protocols into requirements, lead meetings, coordinate stakeholders, and develop solutions amid changing priorities. The role requires project management experience in SDLC environments, knowledge of EDC, eConsent, eCOA, clinical guidelines, and clinical data management processes.
Summary Generated by Built In

At Castor, we’re modernizing the backbone of clinical research

Clinical trials are the gatekeepers of human health, yet the industry is still bogged down by fragmented, manual processes that can waste time and exclude patient populations. At Castor, we are building the operating system for the next era of clinical research.

We provide a modular cloud platform designed to run trials end-to-end. Our foundation is a robust Electronic Data Capture (EDC) system, supported by eConsent for recruitment and screening and eCOA to accurately capture patient reported outcomes. We don’t just stop at data collection; we use Castor Catalyst (our high-precision AI automation) to strip away the manual effort that historically makes research slow and expensive.

How we work: Trust over tracking

We are a remote-first company built on the belief that talented people do their best work when they have the agency to manage their own lives. We believe that high performance requires a foundation of trust, health, and cutting-edge support.

  • Work-life integration: We don't believe in performative presence. We trust you to own your schedule and show up for your team, while also making space for your life outside of work.
  • Deep work & async: We protect your time. We prioritize thoughtful, asynchronous communication so you can focus on solving hard problems without a calendar full of status update meetings.
  • Radical candor: We value the truth over hierarchy. We give and receive direct feedback because that’s how we grow—as individuals and as a company.

Your mission and impact

As a Project Manager you ensure that individual study milestones are met whilst  maintaining high data quality.. You act as a bridge and consultant to the customer, driving  project delivery across all phases of a study, ensuring strategic objectives are met while maximizing customer satisfaction.

You are also  responsible for all assurance activities related to the availability, integrity and confidentiality of customer, business partner, employee and business information in compliance with our information security policies. 

Who are you

  • You are experienced managing a high volume of lower complexity studies.
  • You comfortably guide clients through complex project plans and serve as a trusted advisor.
  • You are comfortable shifting from process following to active solution leading, applying deep critical thinking to every challenge.
  • You remain focused and effective when faced with shifting priorities, rapid change, or undefined project parameters.
  • You act as a high-level consultant to clients, building trust through advocacy and persuasive communication.
  • You proactively navigate risk, identifying downstream impacts early and architecting solutions that safeguard project integrity.
  • You are a self-starter who masters the art of remote collaboration. You value deep work and asynchronous communication to drive results.
  • Giving and receiving feedback are necessary to win as a team. You give and receive direct, data-driven feedback, even when it’s uncomfortable.

What you’ll bring

  • 3+ years of Project Management experience in the Software Development Lifecycle (SDLC).
  • Understanding of EDC/CDMS, eConsent and eCOA solutions and services.
  • A passion for positive, customer-focused outcomes achieved with a high degree of ethics and integrity.
  • Highly organized with a strong attention to detail.
  • Able to plan, lead, facilitate, and document effective meetings.
  • A collaborative and resourceful approach, with a “can do” attitude and voracious appetite to learn and grow.
  • Relevant understanding of clinical guidelines: ICH-GCP - Good Clinical Practice, FDA 21 CFR Part 11, and relevant GXP Regulations and Guidances.

It would be good if you had:

  • A solid understanding of medical terminology, specifically in the clinical trials space.
  • Ability  to understand clinical protocols and translate these into client requirements/scope.
  • Knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology).
  • PMP, PRINCE2, or other Project Management certification.
  • Life science or IT degree or another suitable degree.

Accepting candidates +2/-2 CET. At this time, we cannot accept applications from France, Germany, Spain, or Switzerland.

How we invest in you

High performance isn't sustainable without real support. We provide the infrastructure you need to stay healthy, focused, and rewarded.

  • Rest is non-negotiable: Unlimited annual leave with 25-day minimum. We don’t just allow time off; we expect you to take it.
  • Downtime weeks: Once a quarter, the whole company shifts gears. No new shipping—just a week for deep focus, learning, or catching up so we can start the next quarter fresh.
  • AI-first culture: We provide the tools and training to ensure you’re spending your energy on high-value work, not manual repetition.
  • Real ownership: All Castor team members are offered options through our Employee Stock Option Plan (ESOP).
  • Comprehensive wellbeing: Free access to Open Up for mental health, specialized sleep courses (for you and your family), and a budget to make your home office a place you actually want to be.
  • Annual bonus: A guaranteed "Happy Holidays" bonus every December.

Compensation at castor

Castor is a remote, globally distributed company, and as such we use location based salary bands. We believe compensation should be fair and transparent, without unnecessary complexity. For us, compensation means salary + equity + benefits, all of which are designed to support you in doing your best work, wherever you are. This position is open to candidates across multiple regions.

Belonging at Castor

We build products to make research accessible to everyone, and we believe our team should reflect that same diversity.

Our remote setup is designed to support you as a whole person—your family, your mental health, and your authentic self.

We don't care about your background as much as we care about your perspective and your expertise. We strongly encourage applications from women, people of color, and the LGBTQ+ community. Please feel free to share the pronouns you use (for example she/her/hers, he/her/his, they/them/theirs, etc.).

Skills Required

  • 3+ years of Project Management experience in the Software Development Lifecycle (SDLC)
  • Experience managing a high volume of lower-complexity studies
  • Experience guiding clients through complex project plans
  • Understanding of EDC/CDMS, eConsent, and eCOA solutions and services
  • Strong organization and attention to detail
  • Ability to plan, lead, facilitate, and document effective meetings
  • Understanding of ICH-GCP, FDA 21 CFR Part 11, and relevant GxP regulations and guidance
  • Knowledge of medical terminology in the clinical trials space
  • Ability to understand clinical protocols and translate them into client requirements and scope
  • Knowledge of clinical data management processes, including SAE reconciliation and external data vendor reconciliation
  • PMP, PRINCE2, or another project management certification
  • Life sciences, IT, or another suitable degree

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The Company
HQ: Amsterdam
230 Employees
Year Founded: 2011

What We Do

At Castor, we believe in the power of clinical research and the power of technology. And we know that together, these forces can help extend human healthspan. To achieve this reality, we must make patient-centered clinical trials a possibility for everyone, anywhere in the world. That's why we are using technology to capture the world's research data and optimize each activity of a clinical trial. From recruitment to monitoring, our modular clinical trial platform makes it easier to design and deploy trials, enroll and engage patients, collect data and analyze results. Each module can be used individually or in unison with others, providing the ability to customize each solution to fit your needs, and grow at your own pace. That’s delightful for patients, effortless for study teams, risk-free for sponsors.

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