Senior Clinical Project Manager - Nephrology (Europe)

Das ist der Job

At the heart of our success is our ability to combine global reach with local knowledge.

Darum lohnt es sich

Our on‑the‑ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. About The Role We are seeking an experienced Senior Project Manager to join our growing team in Europe. Provide mentorship and guidance to junior project team members.

Participate in internal and external project team meetings to ensure alignment and success. 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. Employee Well‑being: 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 exposure to diverse projects and clients. Emerald Clinical Trials is a global, full‑service Contract Research Organization with a rich heritage in the Asia‑Pacific region.

We advance clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post‑marketing. Our therapeutic expertise spans renal , cardiometabolic , and oncology —areas where we significantly impact global health.

By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need. This home‑based role offers flexibility while empowering you to lead global and regional clinical trials across multiple therapeutic areas.

The ideal candidate will have experience managing renal clinical trials and a strong background in project leadership, financial oversight, and strategic trial execution. Your Responsibilities Provide strong, independent leadership for assigned clinical projects, ensuring successful execution.

Serve as the primary point of contact for clients, vendors, and internal stakeholders. Oversee study management activities, including site selection, initiation, monitoring, and closeout. Develop and maintain study timelines, budgets, and project plans, ensuring adherence to scope.

Mitigate risks and proactively address challenges to keep projects on track. Ensure compliance with ICH‑GCP, regulatory guidelines, and company SOPs. Manage vendor relationships and study‑specific contracts. Support proposal development, bid defense meetings, and business growth initiatives.

About You 5–7 years of project management experience in clinical research, preferably in a CRO or pharmaceutical environment. Strong nephrology clinical trial experience is required. Prior experience in clinical site management and CRA roles is preferred. Proven expertise in budget management, forecasting, and contract oversight.

A proactive, solutions‑oriented mindset with excellent communication and leadership skills. Strong knowledge of ICH‑GCP and regulatory requirements (FDA, TGA, EMA, etc.). Proficiency in Microsoft Office (Word, Excel, PowerPoint, Adobe Acrobat). Ability to manage multiple priorities in a fast‑paced, global environment.

A degree in a relevant scientific, healthcare, or project management field. Why Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees.

Here’s What Makes Us Stand Out Purpose‑Driven Work: Contribute to clinical trials that genuinely improve lives, focusing on therapies in renal, cardiometabolic, and oncology. Global Reach, Local Expertise: Connect with local communities, building trust and meaningful engagement for every trial.

Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. 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. We are an equal‑opportunity employer and encourage applications from all qualified candidates. #J-18808-Ljbffr