Job opening

DICE is a leading CRO with over 35 years of experience focused that serves biotech and big pharma companies in Europe and the US. In order to support our growth, we are looking to hire a Senior Clinical Project Manager.

As a Senior Clinical Project Manager you will be the driving force behind the successful execution of clinical trials for our sponsor clients. You’ll manage multiple studies across various therapeutic areas with a focus on oncology , ensuring delivery on time, within budget, and in full compliance with regulatory standards and the QMS system of DICE. This role demands strategic oversight, operational excellence, and client-facing and vendor facing finesse.

Responsibilities

Project Oversight

• Lead the planning, initiation, execution, and closure of clinical trials
• Develop and manage project quotes, project timelines, budgets, and resource allocation
• Ensure adherence to protocol, GCP, regulatory requirements and the DICE QMS system
• Identify project risks and implement mitigation strategies
• Monitor quality metrics and ensure continuous improvement

Vendor Coordination and operational oversight

• Oversee selection and management of third-party vendors, including contracting, budgets and invoices.
• Operational oversight of clinical operations, regulatory and pharmacovigilance teams that are either contracted or collaborate on the projects

Team Leadership

• Coordinate cross-functional teams including, biostatistician, data managers, medical monitors and medical writers
• Provide guidance, mentorship, and performance feedback to project team members

Client & Stakeholder Management

• Serve as the primary point of contact for sponsor clients throughout the study lifecycle
• Build strong relationships and ensure client satisfaction through proactive communication and issue resolution

Reporting & Documentation

• Maintain accurate project documentation and ensure timely reporting to clients and internal leadership
• Prepare study status reports, dashboards, and presentations

Qualifications and skills

• Master’s degree in Life Sciences, Nursing, Biomedical sciences, Pharmacy, or related field or similar through experience.
• Minimum 10 years of clinical research experience, with at least 5 years in a CRO project management role
• Proven track record managing Phase I–IV trials across multiple therapeutic areas.
• Experience in oncology is considered as a plus.
• Strong understanding of ICH-GCP, FDA, EMA, and other global regulatory guidelines
• PMP or equivalent certification preferred
• Excellent communication, negotiation, and organizational skills
  Attention to detail, ability to work independently and able to distinguish important points from details
• Stress resistant
• Proficiency in project management tools (e.g., MS Project, CTMS, eTMF systems)

Our offer

DICE is a clinical research organization (CRO), that supports clinical studies for pharmaceutical and biotechnology companies. We offer full service projects delivery to our sponsors, and have an internal team that is specialised in clinical data management, bio statistics, central imaging review, medical writing and medical monitoring.

If you work with us then we can offer this package:

• A driver’s seat position in clinical research
• A young and dynamic work environment with close contact to our sponsors
• Possibility to grow with and within our company
• An attractive salary with lots of extras, including a long term incentive plan based on company targets
• An easy to reach office
• Possibilities to work from home
• A personal development path with tailored courses and training

Take your career to the next level, and apply now. Email mona.eerdekens@dice-cro.com