We are seeking an experienced Senior IT Project Manager (m/f/x) to lead and drive digital transformation initiatives. You will be responsible for overseeing company-wide technology projects, ensuring successful execution, and aligning IT strategies with business objectives. You will have the opportunity to thrive in a dynamic biotech environment, adapting to evolving industry needs and regulatory requirements. These tasks are waiting for you: Lead end-to-end project management for digital transformation initiatives, including planning, execution, monitoring, and deliveryDevelop and maintain detailed project plans, timelines, budgets, and risk management strategiesCollaborate with business leaders, IT teams, and external vendors to define project scope, objectives, and deliverablesWork closely with third-party vendors to ensure project deliverables meet quality and timeline expectationsManage stakeholder communication, providing regular updatesDrive initiatives that contribute to measurable business improvements and successful project outcomesDetails about the workplace:Type of contract: indefinite + full timeVacation: 30 days / yearWorking hours: 40 hours / weekAn opportunity to lead the digital transformationA collaborative and inclusive work environment with a diverse team of expertsThis completes your profile:University degree in information technology, business or a related field, or equivalent qualification5-7 years of extensive experience with IT Project Management and strong understanding of methodologiesIdeally experience of working in a regulated environment (e.g., Pharma, MedTech, etc.)Effective communicator with a strong hands-on mentalityFluent in English; intermediate German skills are preferred Information about our client: Our client is a global clinical-stage biopharmaceutical company that discovers and develops drugs. With their innovation-driven team, the company focuses on vaccines, innovative cancer immunotherapies and protein-based therapies. If you are passionate about leveraging technology to transform businesses and have a track record of delivering complex IT projects, we'd love to hear from you!

Are you a hands-on pharmacovigilance (PV) professional with a robust skill set, ready to roll up your sleeves and make an impact? SciPro are collaborating with one of our partners on a critical search for a Deputy QPPV for EMEA. The company is a fast-growing rare disease organisation with a highly collaborative culture, bringing innovative products to patients globally.This is an operational, solution-driven role with QPPV oversight globally to drive impact as a leader within the small global PV team.Your work will span key projects, including:Developing a QPPV oversight report to enhance process governance.Driving PV process improvements and ensuring effective oversight across interfaces.Implementing QPPV training to educate the wider organisation.Collaborating cross-functionally to strengthen global pharmacovigilance strategies.Key Requirements:Experienced in global PV teams with strong exposure to QPPV responsibilities.Thrives in a flat-structured, matrix environment, where collaboration and teamwork are key.Strong communication skills.Excellent critical thinking skills to assess situations and present effective solutions.If you're looking for a role where you can truly shape global PV oversight, contribute strategically, and work in a supportive and dynamic environment, we'd love to hear from you.Apply today to be part of a mission-driven rare disease organisation making a difference

Senior Manager, Pharmacovigilance (Consultant) - Remote UK Are you a proactive and detail-oriented pharmacovigilance professional looking to make an impact across diverse therapeutic areas? SciPro is hiring a Senior Manager, Pharmacovigilance (Consultant) to lead and enhance our drug safety systems, ensuring compliance and innovation for a Rare Disease Pharmaceutical Company. About the RoleYou'll drive all pharmacovigilance and drug safety activities, collaborating with cross-functional teams and external partners. This is your chance to work with cutting-edge technologies in metabolic, immunology, and neurology fields while directly contributing to our growth and the patients we serve.Why apply?In this position you'll have the opportunity to shape the future of pharmacovigilance, working on impactful projects that benefit patients worldwide. We value innovation, collaboration, and professional development, and we're committed to supporting your growth. The company is continually having year on year growth and this position has the potential to offer further skills and development as projects grow.What You'll DoPharmacovigilance LeadershipOversee daily PV operations, including safety reporting, risk management, and clinical trial support.Manage PV systems, processes, and SOPs, ensuring compliance and continuous improvement.Build strong partnerships with third-party providers, customers, and health authorities.Strategic Departmental SupportShape the department's strategy and operational plan.Share expertise as a PV Subject Matter Expert, providing training and guidance.Drive process improvements and collaborate across departments to enhance efficiency.Team DevelopmentLead and mentor team members, fostering a culture of growth, creativity, and excellence.Coordinate training and professional development for direct reports and junior staff.What You'll BringQualifications:Bachelor's degree or higher in a Life Science discipline.4+ years of pharmacovigilance experience within CRO or pharma settings.Skills:Exceptional communication and negotiation abilities.Proactive, self-starter mindset with strong analytical and problem-solving skills.Expertise in project management and attention to detail under pressure.Proven ability to build relationships and manage teams effectively.