PJob Title: strongHead of Clinical Operations /strong /ppstrongLocation: /strong Spain /ppstrongReports To: /strong Chief Operating Officer (COO) / Chief Executive Officer (CEO) /ppstrongAbout Us: /strong /ppOur partner is an innovative and rapidly growing Contract Research Organization (CRO) dedicated to providing high-quality clinical research services to the pharmaceutical, biotechnology, and medical device industries. With our headquarters in the United States and an expanding presence across Europe, we are at the forefront of driving clinical trial excellence in emerging markets. We are seeking a dynamic and experienced strongHead of Clinical Operations /strong to lead and scale our clinical operations globally. /ppstrongPosition Overview: /strong /ppAs the strongHead of Clinical Operations /strong, you will be responsible for the strategic direction, execution, and oversight of all clinical operations activities for our growing portfolio of clients. You will lead our clinical operations teams across the US and EU, ensuring that clinical trials are executed efficiently, in compliance with regulatory requirements, and within budget and timelines. This is a senior leadership role that will require a deep understanding of clinical trial management, strong cross-functional collaboration, and a passion for scaling operations in a fast-paced environment. /ppstrongKey Responsibilities: /strong /pullistrongStrategic Leadership: /strong /lili Develop and execute the clinical operations strategy to support the growth of the organization, ensuring alignment with overall corporate goals and objectives. /lilistrongGlobal Operations Oversight: /strong /lili Lead and manage clinical trial operations across multiple regions, ensuring seamless collaboration between teams in the US and EU. Provide oversight of trial progress, timelines, and budgets. /lilistrongTeam Leadership Development: /strong /lili Build and lead a high-performing global team of clinical operations professionals, including clinical project managers, clinical research associates (CRAs), clinical trial managers (CTMs), and other operational staff. Foster a culture of collaboration, accountability, and continuous improvement. /lilistrongClinical Trial Execution: /strong /lili Oversee the planning, initiation, execution, and closeout of clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory requirements, and industry standards. /lilistrongClient and Stakeholder Management: /strong /lili Develop and maintain strong relationships with key clients, ensuring the successful delivery of clinical trials that meet or exceed client expectations. Serve as the primary point of contact for clients, presenting trial progress and addressing issues as they arise. /lilistrongRegulatory Compliance Risk Management: /strong /lili Ensure that clinical trials are conducted in compliance with all applicable regulatory requirements, including ICH-GCP, FDA, EMA, and local regulations. Identify and mitigate risks related to clinical trial operations. /lilistrongBudget Resource Management: /strong /lili Oversee the financial management of clinical trials, including the creation and monitoring of budgets. Ensure resource allocation is optimized to meet project requirements and timelines. /lilistrongProcess Improvement Innovation: /strong /lili Lead initiatives to improve clinical trial operations, including the adoption of new technologies and tools to streamline processes and improve efficiency. Continuously assess and optimize operational workflows. /lilistrongReporting Metrics: /strong /lili Establish and monitor key performance indicators (KPIs) to assess the performance and progress of clinical trials. Provide regular updates to executive leadership and stakeholders on the status of ongoing trials. /li /ulpstrongQualifications: /strong /pullistrongEducation: /strong /liliBachelor’s degree in Life Sciences, Nursing, or a related field (advanced degree preferred). /lilistrongExperience: /strong /liliMinimum of 10 years of experience in clinical operations, with at least 5 years in a senior leadership role within a CRO. /liliProven track record of leading global clinical trial operations and managing clinical teams across multiple regions (US and EU). /liliIn-depth knowledge of clinical trial management, GCP, regulatory guidelines, and industry best practices. /lilistrongSkills: /strong /liliStrong leadership and team management skills, with the ability to inspire and motivate cross-functional teams. /liliExcellent communication, presentation, and interpersonal skills. /liliDemonstrated ability to manage complex clinical trials and deliver results on time and within budget. /liliProficient in clinical trial management systems (CTMS), eClinical technologies, and related software tools. /liliStrong analytical and problem-solving abilities. /lilistrongTravel Requirements: /strong /liliOccasional travel to Europe and other international locations as required. /li /ulpstrongWhy Join Us: /strong /pullistrongGrowth Opportunities: /strong Be part of an exciting, fast-growing CRO with the chance to shape the future of clinical operations in an emerging global market. /lilistrongDynamic Culture: /strong Join a collaborative and innovative team that values creativity, excellence, and a patient-centric approach to clinical research. /lilistrongImpact: /strong Make a significant impact by contributing to the successful delivery of clinical trials that drive the development of life-saving therapies and treatments. /li /ul