Clinical Lead | Clinical Trial Manager - Renal

Emerald Clinical; Lisboa; À distance; EUR 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Competitive compensation

Hybrid or remote work

Career growth

Employee wellbeing

Global opportunities

Résumé du poste

Emerald Clinical seeks an experienced Clinical Lead to join our Europe team. This home‑based role offers flexibility while leading global and regional trials across multiple therapeutic areas.

The ideal candidate will have hands‑on trial management experience, strong project leadership, GCP knowledge, and a proven ability to coordinate sites, monitors, investigators, and sponsors. Willingness to travel up to 20% is required.

Qualifications

• Renal experience is mandatory.
• Bachelor’s degree in science field; RN preferred; 1–2 years as Clinical Trial Manager/Lead.
• CCRA/CCRP certification is strongly preferred; strong knowledge of GCP and FDA regulations.

Responsabilités

• Oversee trials from start‑up to close‑out.
• Lead site selection and feasibility with CRAs and investigators.
• Manage timelines, budgets and deliverables.
• Provide protocol oversight for initiation, monitoring, and progress.
• Collaborate with sponsors, investigators and project teams.
• Ensure compliance with GCP, FDA regs and SOPs.
• Train and mentor CRAs and site staff.

Connaissances

Renal experience

Trial management experience

Leadership & communication

Formation

Bachelor’s degree in science field (RN preferred)

CCRA/CCRP certification preferred

Description du poste

About the Company

Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‑to‑end clinical trial solutions across all phases, offering Phase I-IV and real‑world studies. With over 25 years of experience and a world‑renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality. Our 800+ employees across Asia‑Pacific, Europe, and the Americas are embedded in communities worldwide, driving faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

We are seeking an experienced Clinical Lead to join our growing team in Europe. This home‑based role offers flexibility while providing the opportunity to lead global and regional clinical trials across multiple therapeutic areas. The ideal candidate will have experience managing clinical trials and a strong background in project leadership, clinical operations, and strategic trial execution.

Your Responsibilities

• Oversee clinical trials, ensuring successful execution from start‑up to close‑out.
• Lead site selection and feasibility assessments, working closely with CRAs and investigators.
• Manage study timelines, budgets, and deliverables, ensuring adherence to project objectives.
• Provide oversight on protocol administration, site initiation, monitoring, and study progress.
• Collaborate cross‑functionally with internal and external stakeholders, including sponsors, investigators, and project teams.
• Ensure compliance with GCP, FDA regulations, and company SOPs.
• Train and mentor CRAs and site staff, ensuring protocol adherence and data integrity.

About You

• Renal experience is mandatory.
• Bachelor’s degree in a science‑related field (RN preferred) with industry experience, including 1‑2 years as a Clinical Trial Manager/Clinical Lead.
• Strong background in monitoring and site management, preferably with experience in oncology or other complex indications.
• CCRA or CCRP certification is strongly preferred.
• Excellent knowledge of GCP, FDA regulations, and clinical trial best practices.
• Ability to manage multiple projects, timelines, and stakeholders efficiently.
• Strong leadership, problem‑solving, and communication skills.
• Willingness to travel up to 20% as required.

Why Join Us?

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

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: Teams 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.

What We Offer

• Competitive Compensation: A tailored salary and benefits package.
• Flexibility: Hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to learning opportunities and a global network of scientific leaders.
• Employee Wellbeing: Programs and initiatives to promote work‑life balance, health, and team connection.
• Global Opportunities: Exposure to diverse projects and clients.

We are an equal‑opportunity employer and encourage applications from all qualified candidates.