Contract Cyber Security Project Manager

as a 'Freelance Clinical Trial Project Manager' where the key responsibility would be to manage the CRO tasked with the trial and all associated groups to ensure the success of the project. This assignment requires full time availability (1.0FTE); it can be performed remotely ideally within the EU (the UK is also possible) and it will last for a duration of 6 months with a start date of January 2026 being preferred. Responsibilities included:Ensure patients within the trials follow all protocols set out (dosed) Full management of the CRO partners throughout the projectEffective coordination on a cross-functional basis which includes Regulatory, Quality, Supply Chain etc. Ensure compliance throughout the project to all necessary guidelines Manage key stakeholders throughout the projectAble to consider all avenues affecting the success of the project and devise solutions to any bottlenecks foundEnsure the overall success of the project as a key project leader Skills requiredMust be, We are expanding our team here at Rayner! Reporting into the Global Director, Clinical Research, the Clinical Operations Manager will be a truly collaborative professional, working closely with KOLs, investigators, and ophthalmic research organizations to provide scientific..., Summary:We are seeking an experienced and proactive Clinical Research Project Manager to join our growing team. The role involves leading the successful coordination and delivery of clinical trials across multiple sites. You will be responsible for overseeing the study..., We're looking for a Contract Cyber Security Project Manager to support one of our retail clients in an exciting Cybersecurity project. As the Contract Cyber Security Project Manager, you'll ensure the programme is delivered to a high standard, providing strong project..., As a Program Director of The Marketing Practice's integration programme you will be responsible for leading, aligning and driving the various programmes of work that are ensuring the six historic businesses that have been merged into TMP are one single coherent organisation..., An experienced Clinical Data Manager is required to join a European consultancy on an initial 12 month contract. The successful candidate will work across projects for a global pharmaceutical company. Full and part-time opportunities available. Applicants must be based in...

educated within a life science discipline to at least a BSc or higher Proven experience working as a Clinical Project Manager or higher is a must Ideally skilled in the Biological space with Gene therapy exposure being of particular interestMust demonstrate key experience managing CRO partners; working on early phase activities (Phase 1) all within the UK/EU Fluency in English is a mustCan perform the project as set out within the job description Additional InformationWe celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or, Clinical Operations LeaderQualifications:Strong personality with excellent ability to navigate cross-functional relationships.Experience in biotech or pharmaceutical environments, leading clinical trials end-to-end.Proven capability managing large, complex budgets.Excellent...

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.Job descriptionProPharma is currently supporting a development organisation in the Biological space with support for their early phase (phase 1) Clinical trial activities within the EU. This project is to lead, About 52North 52North is a medical technology company on a mission to make emergency care safer and more effective. Awarded breakthrough status for its first product Neutrocheck® by the UK Government in 2024, we build innovative diagnostic and digital solutions to transform..., THE BIG PICTUREBernadette is a digital experience agency and part of VCCP Group. VCCP is the challenger agency for challenger brands, with over 1500 people around the world. We offer full-service marketing and brand experience solutions from advertising to media buying,..., About Summit:Ivonescimab, known as SMT112, is a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule....