ppAt bEmerald Clinical Trials /b, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing. /p pOur therapeutic expertise spans brenal /b, bcardiometabolic /b, and boncology /b - areas where we make a significant impact on improving global health. /p pAt the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results - bringing therapies to patients in need. /p h3About The Role /h3 pWe are seeking an experienced bManager, Study Start Up /b to lead and scale our centralised study start-up function across the globe. This is a critical leadership role responsible for delivering efficient, high-quality start-up activities across multiple clinical trials while driving strategic improvements and operational excellence. /p pAs the centralised start-up team continues to grow, this role will provide dedicated leadership, ensuring strong line management, clear strategy, and consistent best practices across all start-up activities. You will play a key role in supporting business development efforts, contributing to proposals, and ensuring that start-up capabilities align with client expectations and organisational growth objectives. /p pThis position is instrumental in improving operational efficiency, enabling billable teams to remain focused on study execution, and ultimately enhancing client satisfaction and delivery performance. /p h3Your Responsibilities /h3 ul liProvide line management and leadership to the global start-up team, including coaching, development,



and performance management /li liDefine and implement the overall start-up strategy, ensuring alignment with global objectives and regional needs /li liOversee end-to-end study start-up activities, including country/site feasibility, submissions, ethic approvals, and activation timelines /li liDrive process optimisation and best practices to increase efficiency, consistency, and quality across all start-up deliverables /li liCollaborate with Business Development and Proposals teams to support bid defenses, feasibility input, and strategic study planning /li liAct as a key stakeholder in client engagement, ensuring start-up expectations are clearly defined and met /li liMonitor and report on start-up KPIs, timelines, and risks, implementing mitigation strategies as needed /li liPartner cross-functionally with Clinical Operations, Regulatory Affairs, Project Management, and external vendors /li liSupport business growth initiatives by ensuring scalable and high-performing start-up operations /li liEnsure compliance with ICH-GCP, regulatory requirements, and company SOPs /li liChampion a culture of continuous improvement, collaboration, and accountability /li /ul h3About You /h3 pTo be successful in this role, you will have: /p ul liDegree in a science, healthcare, or related discipline /li liExtensive experience in clinical trial start-up within a CRO or pharmaceutical environment /li liProven leadership experience, including line management of remote and global teams /li liStrong understanding of European clinical trial regulations and start-up processes /li liExperience contributing to proposals,



feasibility assessments, and business development activities /li liDemonstrated ability to drive strategic initiatives and process improvements /liliExcellent communication and stakeholder management skills, with the ability to influence at all levels /li liStrong organisational and problem‑solving capabilities in a fast‑paced environment /li liProficiency with clinical systems and Microsoft Office tools /li liWillingness to travel up to 10% /li /ul h3Why Join Us? /h3 pAt 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 integral network of passionate professionals working together to deliver better research and outcomes for millions worldwide. /p h3Here’s What Makes Us Stand Out /h3 ul liPurpose‑Driven Work: Contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology. /li liGlobal Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial. /li liCollaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. /li /ul h3What We Offer /h3 ul liCompetitive Compensation: A tailored salary and benefits package reflecting your experience and expertise /li liFlexibility: Hybrid or remote working options depending on your location /li liCareer Growth: Access to global development opportunities and exposure to leading scientific experts /li liEmployee Wellbeing: Programs designed to support work‑life balance, recognition, and team connection /li liGlobal Opportunities: Work on international studies with diverse clients and teams /li /ul pWe are an equal‑opportunity employer and encourage applications from all qualified candidates. /p /p #J-18808-Ljbffr

📌 Manager, Study Start Up (Madrid)
🏢 Emerald Clinical
📍 Madrid