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CRA Lead

Full Time

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Key Responsibilities

The CRA Lead is responsible for mentoring junior CRAs, managing multiple study sites, and serving as a key liaison between clinical trial sites and study sponsors.

Responsibilities:

Lead CRA teams and oversee site monitoring activities for assigned trials.
Provide mentorship and guidance to CRA I and CRA II team members.
Perform risk-based monitoring and quality control checks to ensure compliance.
Coordinate communication between sites, sponsors, and internal study teams.
Contribute to protocol development and process improvement initiatives.
Manage the Data Driven deliverables through Clinical Tower Software Platform

Qualifications:

Bachelor’s or Master’s degree in life sciences or nursing.
4-6 years of experience in clinical research with site monitoring experience.
Proven leadership and training abilities.
Strong knowledge of risk-based monitoring strategies.
Must have some AI Literacy within the Clincal Trials Space.

Ready to Grow in Clinical Project Management?

This role offers growth opportunities into other CRA positions. Join CiNTL Pharma B.V. and build a career in data-driven clinical trial execution.

About You

You are an ambitious professional looking to gain expertise in developing your career within the clinical operations management space.

You are:

Highly organized, data driven and capable of multitasking in a fast-paced environment.
A collaborative team player, ready to support cross-functional efforts.
Detail-oriented, ensuring accuracy in trial documentation and tracking.
Adaptable and eager to learn, embracing new technologies and methodologies.
Committed to quality and compliance, ensuring excellence in clinical trial execution.

Locations & Work Environment

CiNTL Pharma B.V. offers hybrid work flexibility, allowing a blend of on-site collaboration and remote work to optimize productivity. Our offices foster a tech-driven and collaborative work environment.

About CiNTL Pharma B.V.

CiNTL Pharma B.V. is a leading contract research organization (CRO) specializing in data-driven phase I-IV clinical trial management. With cutting-edge analytics, predictive modeling, and AI-driven solutions, we enable sponsors to accelerate drug development and enhance patient outcomes. Based in Utrecht Science Park, The Netherlands, we are committed to revolutionizing clinical research.

Our Commitment to Diversity, Equity, and Inclusion

At CiNTL Pharma B.V., we embrace diverse perspectives and innovation. We are an equal opportunity employer, fostering an inclusive workplace for all employees and applicants.

Join Us

If you are ready to advance your career in clinical project management, apply today and be part of CiNTL Pharma’s pioneering team!Lead end-to-end business development from prospecting and proposal creation to contract negotiation and close.

Clinical Project Manager I

Career Growth

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As a Clinical Project Manager I (CPM I) at CiNTL Pharma B.V., you will be responsible for supporting the planning, execution, and coordination of phase I-IV clinical trials under the guidance of senior project management. You will assist in project tracking, stakeholder communication, and ensuring compliance with regulatory and quality requirements.

Responsibilities:

Assist in the development of project timelines, milestones, and deliverables in collaboration with senior project managers and cross-functional teams.
Support site selection, activation, and patient recruitment strategies to meet project objectives.
Monitor project status, track key performance indicators (KPIs), and report progress to project leads.
Participate in study team meetings, preparing agendas, minutes, and follow-up action plans.
Assist in risk assessment and mitigation planning to ensure project continuity and compliance.
Collaborate with vendors, clinical sites, and internal stakeholders to ensure smooth trial operations.
Maintain trial documentation, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory standards.

Qualifications:

Bachelor’s degree in life sciences, clinical research, or a related field.
Minimum 1-2 years of experience in clinical research, project coordination, or trial management.
Basic knowledge of clinical trial methodologies, GCP guidelines, and regulatory requirements.
Strong organizational, communication, and problem-solving skills.
Proficiency in project tracking tools and Microsoft Office Suite. Especially in the many different eclinical software tools that apply to project management.
MS Project is a must
PMP certification is a must. Do not apply if you do not have this certification.

Ready to Grow in Clinical Project Management?

This role offers growth opportunities into Clinical Project Manager positions as you gain experience. Join CiNTL Pharma B.V. and build a career in data-driven clinical trial execution.

About You

You are an ambitious professional looking to gain expertise in clinical project management. You are:

Highly organized, analytical and capable of multitasking in a fast-paced environment.
A collaborative team player, ready to support cross-functional efforts.
Detail-oriented, ensuring accuracy in trial documentation and tracking.
Adaptable and eager to learn, embracing new technologies and methodologies.
Committed to quality and compliance, ensuring excellence in clinical trial execution.
AI Literacy, is a key component to have.

Locations & Work Environment

About CiNTL Pharma B.V.

Our Commitment to Diversity, Equity, and Inclusion

At CiNTL Pharma B.V., we embrace diverse perspectives and innovation. We are an equal opportunity employer, fostering an inclusive workplace for all employees and applicants.

Join Us

If you are ready to advance your career in clinical project management, apply today and be part of CiNTL Pharma’s pioneering team! Driven By Data, Led by Compassion.