Senior Clinical Trial Manager - Oncology - IQVIA Biotech

FPI Is Hiring | R&D Formulation Supervisor Future Pharmaceutical Industries (FPI) is looking for an experienced and motivated R&D Formulation Supervisor to join our team! 📌 Job Requirements: Bachelor’s degree in Pharmacy. 5–7 years of relevant experience in pharmaceutical formulation and R&D. Strong knowledge of pharmaceutical formulation and product development. Good analytical and problem-solving skills. Strong team management, communication, and organizational skills. 📍 Location: FPI Plant – Badr City, Egypt. 📩 To Apply: Please send your updated CV to hr6@future-eg.com with the subject line: R&D Formulation Supervisor. Show more

Job Summary We are seeking an experienced and highly motivated Senior Consultant – Public Health & Patient Support Programs to lead and support the design, implementation, monitoring, and evaluation of public health initiatives and patient support programs (PSPs). The successful candidate will provide strategic and operational expertise across healthcare projects, collaborating with government entities, healthcare providers, pharmaceutical companies, patient advocacy groups, and other stakeholders to improve patient outcomes and access to care. The Senior Consultant will play a key role in driving program excellence, ensuring compliance with regulatory and quality standards, and delivering measurable health outcomes through innovative, patient-centric solutions. Key Responsibilities Strategic Program Development Lead the design, planning, and implementation of public health programs and patient support initiatives. Conduct healthcare landscape assessments, needs analyses, and stakeholder mapping to identify gaps and opportunities. Develop strategic recommendations to improve patient access, adherence, persistence, and health outcomes. Support business development activities, including proposal development, technical writing, and client presentations. Program & Project Management Oversee end-to-end management of patient support and public health projects, from initiation through closure. Develop project plans, timelines, budgets, risk registers, and governance frameworks. Monitor project performance against agreed KPIs, deliverables, budgets, and timelines. Identify operational challenges and develop mitigation and improvement strategies. Stakeholder & Client Engagement Build and maintain strong relationships with healthcare professionals, government authorities, payers, patient associations, NGOs, and pharmaceutical partners. Facilitate stakeholder meetings, workshops, and advisory boards. Serve as the primary point of contact for clients and key project stakeholders. Monitoring, Evaluation & Reporting Design and implement monitoring and evaluation frameworks for public health and patient support initiatives. Analyze healthcare and program performance data to generate actionable insights. Prepare reports, dashboards, presentations, and executive summaries for clients and leadership. Present project outcomes and recommendations to senior stakeholders. Quality & Compliance Ensure programs comply with local regulations, ethical standards, pharmacovigilance requirements, data privacy regulations, and company SOPs. Support quality assurance activities, audits, and process improvement initiatives. Ensure accurate documentation and maintenance of project records. Team Leadership & Mentorship Provide guidance and mentorship to program managers and project teams. Foster a culture of collaboration, accountability, and continuous improvement. Support resource planning and capability development within the team. Required Qualifications Education Bachelor’s degree in Medicine, Pharmacy, Public Health, Healthcare Management, Life Sciences, or a related field. Master’s degree in Public Health (MPH), Healthcare Management, Epidemiology, or a related discipline is preferred. Experience 7–10 years of professional experience in healthcare consulting, public health programs, patient support programs, healthcare operations, or related healthcare services. Proven experience leading large-scale patient support programs and/or public health projects. Experience working with pharmaceutical companies, governmental healthcare entities, NGOs, healthcare providers, or consulting organizations. Demonstrated success in stakeholder management and client engagement. Required Skills & Competencies Technical Competencies Strong understanding of public health principles and healthcare systems. Experience in patient support program design and implementation. Knowledge of healthcare regulations, pharmacovigilance requirements, and patient privacy standards. Advanced project/program management and governance skills. Strong data analysis, reporting, and performance management capabilities. Professional Skills Excellent strategic thinking and problem-solving abilities. Strong leadership and team management skills. Exceptional communication, presentation, and facilitation skills. Ability to manage multiple projects in a fast-paced environment. Strong client-facing and relationship management capabilities. High attention to detail and commitment to quality. Digital Skills Advanced proficiency in Microsoft Excel, PowerPoint, and Word. Experience with healthcare CRM platforms, project management tools, and reporting dashboards is preferred. Knowledge of business intelligence and data visualization tools is an advantage. Preferred Experience Candidates will ideally have experience in: Designing and managing patient access, adherence, and disease management programs. Working on Ministry of Health, national healthcare, or population health initiatives. Conducting healthcare research, needs assessments, and program evaluations. Managing cross-functional teams and multi-stakeholder healthcare projects. Supporting healthcare transformation and patient-centric care initiatives. Key Success Indicators Success In This Role Will Be Measured Through Successful delivery of projects within scope, timeline, and budget. Achievement of defined program KPIs and patient outcomes. High levels of client satisfaction and stakeholder engagement. Effective risk management and issue resolution. Continuous improvement and innovation across program operations. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Show more

Company Description Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. As a Quality Control Senior Specialist, you will perform and review chemical and physical analysis for finished products concerning market release and stability study batches according to their required specifications. The position will be reporting to Quality Control Section Head. You will be required to perform your responsibilities on site, located in our factory in EL Obour City. The job holder will be hired on Legacy Amoun Contract (Part of Arcera). Your responsibilities: Perform and review chemical and physical analysis for finished products of market release and stability study batches. Prepare and review all documents related to finished product chemical and physical analysis for market release and stability study batches. Record all analysis results on SAP system. Perform and review daily calibration for chemical and physical lab equipment’s. Share in preparation working standards used for chemical analysis of finished products if required and control reference samples for finished product. Participate in identifying chemical and physical lab needs for analysis. Participate in investigations and out of specifications related to chemical and physical analysis. Qualifications & Experience: Education: Bachelor’s degree of pharmacy or science (Chemistry) Experience: 3 to 5 years of solid experience in quality department Excellent command of English language is a must ** You can apply for the position through the following link: https://acino.bamboohr.com/careers/803?source=aWQ9MTQ%3D This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you! Show more

The ideal candidate will be responsible for providing care to patients while adhering to compliance standards. This candidate should be able to recognize patient needs and prioritize those needs with the needs outlined by physicians. Responsibilities Assure quality care by adhering to standards set by the physicians Provide care education to patients in person or over the phone Adhere to compliance guidelines throughout processes (OSHA, FDA, HIPAA) Qualifications Must be a Registered Professional Nurse with current licensure CPR, ACLS, and BCLS Certification Knowledge of OSHA, FDA, and HIPAA compliance Candidate must be able to lift and position patients on endoscopy stretcher and transport patients Show more