Manager, Study Start Up

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7gvfjg

At Emerald Clinical Trials, 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.
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Our therapeutic expertise spans renal, cardiometabolic, and oncology - areas where we make a significant impact on improving global health.
At 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.
About The Role
We are seeking an experienced Manager, Study Start Up 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.
As 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.
This position is instrumental in improving operational efficiency, enabling billable teams to remain focused on study execution, and ultimately enhancing client satisfaction and delivery performance.




Your Responsibilities
Provide line management and leadership to the global start-up team, including coaching, development, and performance managementDefine and implement the overall start-up strategy, ensuring alignment with global objectives and regional needsOversee end-to-end study start-up activities, including country/site feasibility, submissions, ethic approvals, and activation timelinesDrive process optimisation and best practices to increase efficiency, consistency, and quality across all start-up deliverablesCollaborate with Business Development and Proposals teams to support bid defenses, feasibility input, and strategic study planningAct as a key stakeholder in client engagement, ensuring start-up expectations are clearly defined and metMonitor and report on start-up KPIs, timelines, and risks, implementing mitigation strategies as neededPartner cross-functionally with Clinical Operations, Regulatory Affairs, Project Management, and external vendorsSupport business growth initiatives by ensuring scalable and high-performing start-up operationsEnsure compliance with ICH-GCP, regulatory requirements, and company SOPsChampion a culture of continuous improvement, collaboration, and accountability
About You
Degree in a science, healthcare, or related disciplineExtensive experience in clinical trial start-up within a CRO or pharmaceutical environmentProven leadership experience,



including line management of remote and global teamsStrong understanding of European clinical trial regulations and start-up processesExperience contributing to proposals, feasibility assessments, and business development activitiesDemonstrated ability to drive strategic initiatives and process improvementsExcellent communication and stakeholder management skills, with the ability to influence at all levelsStrong organisational and problem-solving capabilities in a fast-paced environmentProficiency with clinical systems and Microsoft Office toolsWillingness to travel up to 10%
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.
Here’s What Makes Us Stand Out
Purpose-Driven Work: Contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.Global Reach, Local Expertise: Our 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
We understand that great work happens when people feel valued and supported. xysqume That’s why we provide:
Competitive Compensation: A tailored salary and benefits package reflecting your experience and expertiseFlexibility: Hybrid or remote working options depending on your locationCareer Growth: Access to global development opportunities and exposure to leading scientific expertsEmployee Wellbeing: Programs designed to support work-life balance, recognition, and team connectionGlobal Opportunities: Work on international studies with diverse clients and teams
We are an equal-opportunity employer and encourage applications from all qualified candidates.
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7gvfjg