Project Director

About the Opportunity

Preference will be given to candidates who are available to start at short notice.

About the Role

The Project Director (PD) in Emerald Clinical is responsible for all aspects of study management, oversight and Client Management of portfolio of projects (more than one projects for same or multiple clients) across one or more regions. Project Director (PD) may also provide oversight to one or more projects studies managed by Project Managers or Junior staff. The Project Director will be responsible for overall management and quality of a project or group of projects for a particular client, therapeutic area or other specialty area. Project Director must ensure studies are resourced effectively, managed efficiently, achieve project objectives within allocated budgets and agreed timelines and are conducted to the highest standards of Good Clinical Practice (GCP), regulatory requirements and applicable Standard Operating Procedures (SOP). Manage independently with minimal support from Line Manager. The Project Director mentors/coaches Junior Project Management staff or Clinical Delivery Leads and assists their technical development. Depending on the project, the PD may be named as the Project Lead. As an assigned Project Lead is responsible for all aspects of study management activities including cross functional team leadership and co-ordination, Client communication/ management, financial management and Overall study delivery.

Your Responsibilities

• Analyse monthly financial reports for all allocated projects to identify trends and reasons behind figures, escalate as required.
• Ensure project team understand all aspects of their project finance responsibilities and follow appropriate escalation pathways.
• Maintain project utilization, revenue forecast and recognition, identify and implement strategies for improvement (if required) and escalate any significant concerns to management.
• ...

About You

Bachelor’s or Master’s degree in a science or related field. Experience and expertise in clinical trials research – approximately Eleven (11) years, including Phase I-IV studies. Experience in clinical project management– ideally a minimum of Six (6) years in a project management position; global project management, CRO experience, are preferred. Experience managing global studies and different regions, working across different therapeutic indications, managing full-service studies, worked across early phase to Late phases of clinical trial, is preference. Line management experience in project management or/or clinical operations, is preferable. Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions. Previous experience in clinical trial management software. Excellent working knowledge of current ICH/GCP, ethical and regulatory requirements. Experience in managing vendors and suppliers to successful delivery.

Why Join Us?

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

What We Offer

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.

Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates.