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Company Description Founded in 1919, AUC moved to a new 270-acre state-of-the-art campus in New Cairo in 2008. The University also operates in its historic downtown facilities, offering cultural events, graduate classes, and continuing education. Student housing is available in New Cairo. Among the premier universities in the region, AUC is Middle States accredited; its Engineering programs are accredited by ABET, its Chemistry program is accredited by the Canadian Society for Chemistry, and the School of Business is accredited by AACSB, AMBA and EQUIS. The AUC Libraries contain the largest English-language research collection in the region and are an active and integral part of the University's pursuit of excellence in all academic and scholarly programs. AUC is an English-medium institution. Faculty salary and rank are based on qualifications and professional experience. According to AUC policies and procedures, faculty are entitled to generous benefits. Job Description The Department of Psychology welcomes applications for a Professor of Practice position (associate professor-level or professor-level) in counseling or clinical psychology. This is a full-time appointment for a five-year renewable term beginning in Spring 2027. The successful candidate will be expected to contribute to the MA Counseling Psychology program by teaching practicum and internship courses, as well as teaching other counseling psychology theoretical and applied courses. The candidate will also be expected to teach undergraduate courses. The candidate should continue to maintain a program of professional practice. The candidate will be an active member of the psychology faculty and participate in departmental, school, and university service. Requirements Candidates should have a doctorate in counseling psychology, clinical psychology, or related field, preferably with a practitioner-scholar or scientist-practitioner model. Familiarity with U.S. standards in practitioner training and ethics is preferred. We are seeking candidates with experience in diverse or integrative psychotherapy modalities and commitment to cultural competence. As a professor of practice, the candidate should have experience in providing psychotherapy and/or counseling services and a positive reputation in the professional community. The candidate should have previous experience with graduate level teaching and clinical supervision. Expertise in multicultural counseling, career counseling, couples counseling, and/or group counseling is preferred. Valid professional licensure in U.S., Canada, or U.K. is preferred. Additional Information Review of applications will begin immediately and continue until the position is filled. Application Instructions Applicants must submit the following documents via the online system: (a) an updated CV; (b) letter of interest or cover letter for the position that details research/practice focus and experience; (c) statement on teaching goals and philosophy, including courses that the candidate would like to teach/develop; (d) a writing sample or publication; (e) a completed AUC Personnel Information Form (PIF); (f) names and contact information for at least three references familiar with the applicant's professional background. Letters of reference may be sent directly by the referees to psych@aucegypt.edu. Inquiries can be submitted through the online application system or by email to psych@aucegypt.edu. Apply Here PI287057040 Show more

About The Job Responsible for planning, designing, implementing, and reporting for Real-World Evidence (RWE) and Health Economics & Outcomes Research (HEOR) studies. This includes working closely with pharmaceutical, medical device, and diagnostics clients, among others in the development of project-specific methods and project deliverables. The person in this role will also contribute to face-to-face client meetings, teleconference calls, study design, reporting and publication strategies. RWE clinical study scope includes both prospective and retrospective site-based studies, pragmatic trials, decentralized trials, existing secondary data only studies as well as HEOR projects, including literature reviews, meta-analyses, and medical writing activities What You'll Do: Develop Real-World Evidence study protocols/analysis plans, clinical study reports, abstracts and manuscripts ensuring quality and completeness of client deliverables. Lead the conduct of systematic literature reviews and meta-analyses Lead studies involving health economics and outcomes research, including patient/provider perspective, patient reported outcomes measures (PROMs), and cost/benefit analyses Lead studies utilizing existing secondary data sources (e.g., registries, medical claims, electronic healthcare records). Includes programming requirements, analysis and final reporting writing. Interact with clients and team members to determine real-world evidence (RWE) or health economics and outcomes research (HEOR) needs, objectives, and project scope. Participate in internal and client launch meetings to understand the project background, study requirements, timelines and deliverables. Identify appropriate literature, data sources and tools for research to meet client needs. Distill input from clients, clinicians, medical coders, existing data and published literature to assist in the overall study design. Provide epidemiologic input into the statistical analysis plan and output required to meet study objectives. Responsible for ongoing data review from an epidemiologic standpoint. Prepare for and attend expert panels and advisory boards, assist in collection of information and elaboration of meeting reports. Responsible for interpreting clinical outcomes research results and providing epidemiologic expertise in using the most appropriate statistical analysis methods for each study. Work closely with a statistician in the analysis and reporting of clinical study results Prioritize and manage time effectively to meet the needs of multiple clients. Work within project budgets and complete high-quality deliverables in a timely manner. Assist in developing proposals, including providing input into the scientific rationale, methodology, timelines, and budgets. Collaborate with various CTI departments, based on project or study scope What You'll Bring: At least 3 years’ experience in working in outcomes research and/or epidemiology. Master’s degree in public health, epidemiology, health services research, pharmacy, nursing, natural science, biostatistics, or closely related discipline About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI? Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department. Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program. Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market. Important Note In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page. Please Note We will never ask for your bank account information at any point during the recruitment process Show more

Job objective The Center Physician (CP) works under the supervision of Center Manager and the Plasma Operations and Medical Director. The CP plays a critical role in the donation process where he\she has supervision on the whole process and relevant staff to ensure donors safety and plasma quality. The CP ensures that the centers medical staff follows the applicable policies, procedures & regulations. Rotational Shifts (not fixed), 5 working days and 2 days off, 8 working hours (Morning & Night) Key responsibility Ensure the proper selection of suitable plasmapheresis donors according to the effective policies and procedures as well as the as the clinical experience. Observe and confirm compliance of the Center's medical procedures as they affect the safety of the donors and the collected plasma. Responsible for the certification, training and performance of the center medical staff as it pertains to the donor assessment and to compliance with the company's policies and procedures. Provide additional necessary training, re-certification and corrective actions for the center's medical staff, in collaboration with the training department. Perform the required physical examination for donors. Review donors related documents carefully. Carefully explain the Informed Consent and witness the donor's signature on the form. In a private and confidential setting, discuss the high-risk behavior educational material and definitions of high-risk behavior categories in order to provide the donor with the ability to self-exclude from donating. Participate in the notification and counselling of donors found to be positive for various infectious disease markers such as HBV, HIV, HCV, syphilis, and other required tests. Management of Donor Adverse Event Reactions and the appropriate level of care. Timely review of accumulated data to confirm established donor suitability, donor safety and product safety. Review the accumulated laboratory data of SPE, syphilis and Total Protein results in a timely basis, as well as the collection records, to determine whether the donor should be deferred for further donation. Approve a donor whose SPE results were abnormal for plasmapheresis when normal results are obtained. Recommend changes and improvements to Standard Operating Procedures. Provide education sessions to the center medical staff according to the company's Standard Operating Procedures (SOP). Learn, understand and be independent working with the PDS (Plasma Donor System). Follows all cGMP and good documentation practice guidelines. Review the QA reports for timely and appropriate actions on moderate complexity procedures for test problems. Job Requirements Academic experience required Essential: Bachelor's degree in medicine. Preferred: Post graduate studies in Medicine, preferrable. Professional Experience Required Clinical experience. Experience in GxP-regulated environment. Computing Skills Proficiency in all Microsoft Office applications. Personal Skills Clinical skills. Assertiveness and decision-making ability. Quality mindset. Excellent customer service skills. Organized and able to manage time effectively. Ability to work within a highly regulated and fast paced medical environment. Ability to influence and direct center medical staff through effective leadership skills. Ability to understand, explain, follow, and enforce SOPs and protocols. Ability to plan, communicate and execute activities for the improvement of overall operations. Languages Excellent written and spoken English and Arabic. Show more

Supervise and monitor all finishing works at the project site. Ensure that construction and finishing activities are executed according to approved drawings, specifications, and project requirements. Coordinate with subcontractors, suppliers, and other site teams to ensure smooth workflow. Monitor the quality of finishing works and ensure compliance with required standards. Follow up on daily site activities and report progress to the Project Manager / Site Management. Review drawings and coordinate with relevant teams to resolve technical issues. Ensure proper execution of works within the agreed project timeline. Monitor materials used on-site and ensure they meet the required specifications. Identify and report any site issues, delays, or discrepancies and support in finding appropriate solutions. Conduct regular site inspections and ensure proper completion of finishing activities. Coordinate with other engineering disciplines to avoid conflicts and ensure proper project execution. Prepare and maintain daily site reports and required documentation. Requirements Bachelor's degree in Civil or Architectural Engineering. Graduates from 2019 to 2022. Previous experience in finishing works and construction sites is preferred. Good knowledge of finishing materials, construction methods, and site execution. Ability to read and understand engineering drawings. Good communication and coordination skills. Ability to work under pressure and meet project deadlines. Willingness to work at different project locations. Benefits Accommodation: Company-provided accommodation for candidates relocating from outside the project location, when required. Daily Transportation: Transportation from home to the project site and back is the engineer's responsibility. Inter-site Transportation: Transportation between different project sites will be covered by the company or provided through a company vehicle. Salary: To be discussed and determined during the interview based on experience and overall fit. Show more

Welcome to GROW: Our Post Graduate Program at Holcim Egypt. This 1-year program is designed to accelerate your professional growth and provide hands-on experience in your field of interest. This Program Starts on October 15th, 2026 WHO IS HOLCIM? A global leader in innovative and sustainable building solutions, Holcim is enabling greener cities, smarter infrastructure, and improved living standards all over Egypt. With sustainability at the core of our strategy, we are becoming a net-zero company, thriving with our people and communities. Holcim Egypt launched one of the largest cement plants in the MENA region which is located in Ain Al-Sokhna, with a plant capacity of 9.5 MT and 5 state-of-the-art production lines. Through its established business operations in Cement & Ready-Mix concrete; Holcim Egypt has demonstrated its commitment to the provision of sustainable building materials. Qualifications: Civil Engineering Grads. Graduates of 2025 to 2026 ONLY. Completed or postponed military status (Males) Cairo Residents. Show more

ISS International SpA has an open vacancy in Cairo as Junior Civil Design Engineer for fresh graduates at an international company operating in the Oil & Gas Industry. Location: New Cairo Starting date: 01/10/2026; Duration: 30/09/2027, liable to extension; Working schedule: 8 hours a day / 5 days a week; Rotation: Resident Show more