SciPro are partnered with a growing biopharmaceutical company is seeking a Clinical Trial Manager to support the planning and execution of global clinical trials in collaboration with the Director of Clinical Operations. This role is critical in ensuring clinical programs are delivered on time, within budget, and in line with regulatory and quality standards for a best-in-class therapy.The organization is focused on advancing transformative therapies for patients with rare macrophage-mediated diseases. Their mission is to improve patient outcomes by delivering scientifically driven, high-quality clinical programs with speed and precision.Key ResponsibilitiesTrial Management: Lead the development of trial plans, budgets, and timelines; oversee execution and ensure alignment with clinical and regulatory goals.Stakeholder Engagement: Act as the main point of contact for cross-functional teams, investigators, and vendors; drive collaboration and resolve project issues.Compliance & Quality: Maintain GCP and regulatory adherence across all trial activities; manage audits, documentation, and implement risk mitigation strategies.Key RequirementsExperience: Proven background in clinical project management, ideally within biotech or a start-up setting; successful delivery of complex trials from start to finish.Skills: Strong leadership, communication, and project management skills; proficient in tools like Microsoft Project, Excel, and EDC systems.Certifications: PMP or CCRA certification is desirable; ability to mentor and operate within a dynamic, high-performance team environment.

SciPro are partnered with a leading, privately held biopharmaceutical company and leading their search for a Director of Clinical Operations based in the UK to oversee and drive global clinical trial activities for a late-stage development program in rare diseases. This pivotal leadership role focuses on managing complex outsourced trials, ensuring timelines, quality, and regulatory compliance in a fast-paced environment.The company is committed to advancing a best-in-class monoclonal antibody therapy to address unmet clinical needs in rare macrophage-driven diseases. By combining deep scientific expertise with patient-centred innovation, the organization strives to significantly improve patient outcomes and quality of life.Key ResponsibilitiesClinical Trial Oversight: Lead end-to-end global trial planning and execution, managing multiple CROs and vendors, and ensuring delivery on time and within budget.Stakeholder & Team Leadership: Act as a key liaison between cross-functional teams and senior leadership, while mentoring team members and guiding resource allocation.Compliance & Risk Management: Ensure adherence to GCP, ICH, and regulatory guidelines, maintain trial documentation readiness, and proactively manage operational risks.Key RequirementsExperience: Proven track record in clinical project management, ideally within biotech or fast-paced start-up environments; extensive knowledge of trial regulations and processes.Skills: Strong leadership, communication, and analytical skills; adept with tools like CTMS, eTMF, EDC (preferably Medidata RAVE), and Microsoft Project.Mindset: Highly organized, proactive, and flexible with a hands-on approach; comfortable working autonomously and contributing across functional areas when needed.