26 Healthcare Project jobs in Egypt

Clinical Project Lead

EGP100000 - EGP200000 Y MCT-CRO

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Job Description

The Clinical Project Lead (CPL) will work in the Clinical Operations with an emphasis placed on ensuring the highest ethical and clinical standards.

  • The CPL assumes responsibility for an individual project or many projects, for one or more Sponsors and reports on the project level to the Account Operations Manager (AOM) responsible for that Sponsor's account.
  • The CPL is the liaison with the Sponsor and communicates in an optimal way, making sure that the specific Sponsor's objectives are met.
  • The CPL is the leader and the responsible for the project team. The CPL plays an active role in the planning and monitoring of the study.
  • The CPL might be required to act as CRA III and act as back-up CRA where needed.

The Position is for MENA Region

Applicant should have as a minimum:

  • 6 years of experience as a Clinical Project Lead
  • Bachelor's degree in a health-related field
  • Working knowledge of relevant regulations related to clinical research studies, ICH Guidelines and GCP
  • Business proficiency in English & use of Office Suite
  • Excellent organizational and communication skills
  • Detail oriented
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Clinical Project Manager

EGP900000 - EGP1200000 Y PDC CRO

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Job Description

Pharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region. Our clients include pharmaceutical, biotechnology, medical device industries, other CROs, and academic organizations. Our team is experienced in managing clinical projects from beginning to completion, PDC has been recognized among the leaders as Clinical Research Organization in the region.

Due to our successful development, we are looking for highly motivated and responsible candidates for the position of:

Name of position: Clinical Project Manager- Location: Egypt

Essential Functions and Other Job Information

  1. Being and serve as the first point of contact to client.
  2. Coordination and control over the feasibility, start-up, clinical and site-management activities related to a specific clinical trial within the Division.
  3. Strict control over the compliance of study milestones: start, patients' enrolment (overall study) and timelines as per the contract obligations.
  4. Control over budget, issue, task, and time management of the project/s under their supervision.
  5. Oversights of submission/ approval process to EC/ RA.
  6. Communication with sponsors, partner CROs, physicians, third parties and regulatory authorities.
  7. Manages the process of creation, approval of all essential documents developed or tailored in-house as ICF, patient material and translated documents.
  8. Responsible for distribution within the team of final approved version of all essential documents (Protocol, IB, CRF, ICF, etc.).
  9. Initiate qualification and approval, ongoing management, oversight and dealing with all third parties involved in the study; complete re-assessment activities.
  10. Develops and communicates all study specific plans as PMP, monitoring plan, TMF maintenance plan, communication plan, quality plan, project risk matrix (if applicable) as well as any other study-specific instructions and guidelines.
  11. Ensures on time study team trainings, meetings, and customization of study-specific forms and plans.
  12. Control over all logistic procedures related to the study.
  13. Identify changes, work with team members to quantify financial/ time impact and communicate those changes to appropriate personnel.
  14. Ensures the contracting process, when required.
  15. Timely coverage of all assigned trainings.
  16. Adheres to the rules and regulations of ICH-GCP and other regulatory and ethical guidelines and data protection regulations.
  17. Coordinates activities between different stakeholders and determine interim study time points.
  18. Providing any requested internal progress reports and completion of the relevant files.
  19. Preparation and conducting of Investigator Meetings in close collaboration with the client.
  20. Collaboration with internal/ external auditors, co-monitors, or regulatory inspectors in review of files and patient data.
  21. Executes any activities in compliance with applicable SOPs, instructions, and principles.
  22. Development and update of company SOPs and policies in close collaboration with Management.
  23. Support Business Development activities in terms of meetings and budget development as applicable.
  24. Supervises and assesses the performance of team members and provides feedback to respective line manager/ HR for appraisal.
  25. Perform CPL activities as per assigned clinical trials in all cases as deemed necessary by superior management levels, while avoiding risk of conflict of interest.

Education and Experience


• University degree with life science background or equivalent and relevant formal academic/ vocational

qualification.


• At least 6 years of experience in the field of clinical research; Managing at least 5 Interventional CT.

Knowledge, Skills, and Abilities


• Advanced knowledge of GCP guideline and all applicable clinical research requirements


• Proficiency in English language


• Leadership and good sense of teamwork


• Excellent analytical, organizational, negotiation and decision-making skills


• Ability to communicate information and ideas so others will understand; with the ability to listen to

and understand information and ideas presented through spoken words and sentences.


• Good time management and multitasking skills to coordinate several issues simultaneously.


• Solid interpersonal skills


• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.


• Appropriate MS Office Skills


• May interact with others, relating and gathering sensitive information. Interaction includes diverse

groups.


• Performs a wide range of variable tasks as dictated by variable demands and changing conditions based on task prioritization.


• Ability to perform under stress.


• Regular and consistent attendance

Working Conditions and Environment


• Work is performed in an office or clinical environment with exposure to electrical office equipment.


• Often travels/ drives to site locations. Frequent travel both domestic and international.

The Company Offer:

  • Job-specific training

  • Work for successful international company, excellent career development opportunity in a perspective professional field

  • Very competitive remuneration package

  • Additional benefits related to work performance.

Website

The Assigned Country: Egypt

Only short-listed candidates will be contacted for interviews.

Note: By submitting your application, you agree that your personal data will be processed by PDC in accordance with the applicable Data Protection Law and in strictly keeping your confidentiality.

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Clinical Project Lead

EGP120000 - EGP240000 Y GENOVA

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Job Description

Company Description

GENOVA is a global clinical research organization that offers a wide range of clinical drug development services and innovative solutions from Phase I to IV clinical trials and HEOR. We are dedicated to enabling our partners in the pharmaceutical, biotechnology, and medical device sectors to navigate the complexities of drug development and achieve their strategic objectives in European and MEA markets. Our comprehensive services include Clinical Trials Management, Project Management, Site Management, Regulatory Support, Medical Affairs, Medical Writing, Biostatistics, Data Management, Pharmacovigilance, and Market Access Preparation. Based in the EMEA region, our focus is on delivering top-notch quality services to our clients.

Job Summary

GENOVA is a leading global CRO dedicated to accelerating drug development for our clients. We are seeking a dynamic and experienced
Clinical Project Lead - Project based
to oversee the planning, execution, and completion of clinical trials across various therapeutic areas. In this role, you will lead a cross-functional team and serve as the primary point of contact for our clients, ensuring that all projects are delivered on time, within budget, and to the highest quality standards.

Key Responsibilities

  • Project Leadership: Lead and motivate a multidisciplinary team, including Clinical Research Associates (CRAs), data managers, biostatisticians, and medical writers, to achieve project milestones.

  • Study Management: Develop, manage, and execute comprehensive project plans, including timelines, budgets, and resource allocation.

  • Client Communication: Act as the main point of contact for clients, providing regular updates on project status, managing expectations, and proactively addressing any issues or risks.

  • Regulatory Compliance: Ensure all trial activities comply with regulatory requirements, including ICH-GCP (International Conference on Harmonisation - Good Clinical Practice) and relevant local regulations.

  • Risk Management: Identify potential risks to the project and develop and implement mitigation strategies to keep the trial on track.

  • Financial Oversight: Monitor and manage the project budget, ensuring profitability and controlling costs.

  • Quality Assurance: Oversee the quality of all project deliverables, from study documents to data collection, and support internal and external audits.

Qualifications

  • Bachelor's degree in a life science or a related field; an advanced degree (Master's or PhD) is a plus.

  • Minimum of 4-5 years of experience in clinical research, with at least 2-3 years in a project management or leadership role within a CRO or pharmaceutical company.

  • Strong knowledge of clinical trial processes, ICH-GCP, and regulatory guidelines.

  • Excellent leadership, communication, and negotiation skills.

  • Proven ability to manage complex projects, multiple priorities, and cross-functional teams.

  • Project Management Professional (PMP) or other relevant certifications are highly desirable.

Apply now or share your CV at
-

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Local Clinical Project Manager Sponsor-dedicated

EGP900000 - EGP1200000 Y IQVIA

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Job Description

Job Overview:
Local Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial team is delivering quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), and regulatory requirements. Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Site Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level.

Deliverables:

  • Services rendered will adhere to applicable sponsor's SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.
  • Complies with relevant training requirements.
  • Contribute to quality Site Selection
  • Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget
  • Act as primary contact for assigned trial at the country level, may attend/participate in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting.
  • Drive study compliance
  • Contribute to site level recruitment strategy and contingency
  • Delivers competent vendor management at the country level
  • Ensures high standards for study monitoring
  • Contributes to patient understanding of protocol and patient safety
  • Ensures trial subject safety
  • Ensures Inspection readiness
  • Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements and developing therapeutic knowledge enough for role and responsibilities.
  • With focus on quality and compliance, will work closely with CRAs to ensure CAPA is implemented for audits/inspections or any quality related visits. May conduct accompanied site visits with CRAs, if delegated by FM.
  • Ensure accurate finance reporting and trial delivered within budget
  • Keeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals in cooperation with the local Start Up team, if as applicable.
  • May contribute as a trainer of systems/processes or provide input to functional area in process initiatives, if applicable.
  • Full utilization by timely and accurate time reporting.
  • Experience in management and startup of complex Early Phase trials projection with internal matrix clinical teams and sites, as applicable.

Education and Experience Requirements:

  • BA/BS degree.
  • Degree in a health or science related field.
  • 2 years of local trial management or mutually agreed clinical trial experience.
  • Fluency in Arabic and English

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

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Local Clinical Project Manager Sponsor-dedicated - Hybrid

New Cairo IQVIA

Posted 22 days ago

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Job Description

**Job Overview:**
Local Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial team is delivering quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), and regulatory requirements. Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Site Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level.
**Deliverables:**
+ Services rendered will adhere to applicable sponsor's SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.
+ Complies with relevant training requirements.
+ Contribute to quality Site Selection
+ Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget
+ Act as primary contact for assigned trial at the country level, may attend/participate in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting.
+ Drive study compliance
+ Contribute to site level recruitment strategy and contingency
+ Delivers competent vendor management at the country level
+ Ensures high standards for study monitoring
+ Contributes to patient understanding of protocol and patient safety
+ Ensures trial subject safety
+ Ensures Inspection readiness
+ Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements and developing therapeutic knowledge enough for role and responsibilities.
+ With focus on quality and compliance, will work closely with CRAs to ensure CAPA is implemented for audits/inspections or any quality related visits. May conduct accompanied site visits with CRAs, if delegated by FM.
+ Ensure accurate finance reporting and trial delivered within budget
+ Keeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals in cooperation with the local Start Up team, if as applicable.
+ May contribute as a trainer of systems/processes or provide input to functional area in process initiatives, if applicable.
+ Full utilization by timely and accurate time reporting.
+ Experience in management and startup of complex Early Phase trials projection with internal matrix clinical teams and sites, as applicable.
**Education and Experience Requirements:**
+ BA/BS degree.
+ Degree in a health or science related field.
+ 2 years of local trial management or mutually agreed clinical trial experience.
+ Fluency in Arabic and English
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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Project Management

EGP90000 - EGP120000 Y Systems Limited

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Job Description

Key Responsibilities

1. Project Management & Scheduling

  • Lead project planning, execution, monitoring, and closure following
    PMBOK, PRINCE2, or Agile methodologies.
  • Develop and maintain project schedules, timelines, and reports.
  • Prepare and manage project documentation such as
    Charters, WBS, Risk Registers,
    and status updates.
  • Coordinate with stakeholders to ensure projects are delivered on time, within scope, and budget.

2. Data Analytics, Forecasting & Dashboard Creation

  • Perform data analysis to generate insights and support forecasting models.
  • Design and build interactive dashboards using tools such as
    Power BI, Tableau,
    or similar platforms.
  • Monitor KPIs and provide data-driven recommendations to improve performance and decision-making.
  • Translate complex data into clear and actionable insights for stakeholders.

3. Desktop Research & Strategic Analysis

  • Conduct desktop research, benchmarking, and market analysis.
  • Synthesize findings into meaningful insights and recommendations.
  • Support strategy development with comparative analysis and forecasting.
  • Prepare research reports and presentations for senior management.

Qualifications:

  • Bachelor's degree in business administration, Data Analytics, Engineering, or related field
  • 4+ years of proven experience in Project Management and Data Analytics.
  • Hands-on project management experience (PMBOK/PRINCE2/Agile).
  • Proficiency in Power BI, Tableau, or other BI tools.
  • Strong analytical and problem-solving skills, with proven ability to conduct desktop research and deliver actionable insights.
  • Experience in KPI monitoring and forecasting to support decision making.
  • Excellent communication, presentation, and stakeholder management skills.
  • Ability to work independently and manage multiple priorities.
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Project Management

EGP120000 - EGP240000 Y Kantar

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Job Description

We go beyond the obvious, using intelligence, passion and creativity to inspire new thinking and shape the world we live in.

To start a career that is out of the ordinary, please apply.

Job Details

Project Management- Specialist 1

Kantar

Cairo, Egypt

Kantar stands out as a best-in-class data, insights, and consulting company. We understand more about how people think, feel, shop, share, vote and view than anyone else. Combining our expertise in human understanding with advanced technologies. Kantar's 30,000 people based in more than 100 countries help the world's leading organizations succeed and grow.

Nobody knows people better than Kantar. We provide insight and inspiration to help our clients, our people and society to create and thrive in an outstanding world. Our insights colleagues are specialists in comprehending human behavior. With expertise covering brand, innovation, creative, media, commerce, and customer experience, they help clients define what brands should stand for, how to disrupt and renew their offer, how to connect with audiences and how to win with consumers and customers

Role Deliverables:

Direction:

  • Support the day-to-day management of the actual project throughout the project lifecycle in conjunction with Managers.

Efficiency, Quality & Productivity:

  • Deliver on project tasks and activities, ensuring effective management and delivery of projects as per standard methodologies.

Project Management:

  • Fulfill and finalize project tasks within the timeline, ensuring quality standards are met.
  • Implement project schedules and processes.
  • Coordinate between CS and DP on KPI checks and ensure sharing with client service team.
  • React promptly and efficiently to project adjustments to ensure alignment.
  • Assist in collation of project costs.
  • Collate timelines based on project discussions and process for sign-off.
  • Attend debrief/wrap-up meetings and collate information on challenges, takeaways, and highlights.
  • Ensure timely readiness and sign-off of translated questionnaires.
  • Send questionnaire, sample, adverts, videos, and other materials to Scripter.
  • Attend kick-off meetings when required.
  • Follow-up with Scripter for pilot readiness.
  • Brief Supervisors/Field Managers for UAE and KSA jobs.
  • Accompany clients in field visits and attend CLT projects.
  • Final sample to Data Validation team.
  • Deliver final data to analyst teams or suppliers.
  • Liaise with suppliers and communicate project needs.
  • Check Kantar Projects timeline for accuracy.
  • Coordinate and implement translations and supplier quotations.

Costs & Proposals:

  • Proficient user of the costing system.
  • Participate in project proposals and cost collation.
  • Develop and orchestrate approval for incentive requests.
  • Check trip plans and FSOC against project budget and arrange sign-off.

Communication & Relationships:

  • Communicate timely information to managers regarding deadlines or problems.
  • Daily project-related communication with OPS and Suppliers.
  • Share status report updates with CS team and ensure alignment.

Basic Functions:

  • Raise resource issues with managers.
  • Bring up partner concerns and field feedback for timely resolution.

Training:

  • Proactively responsible for own learning and development.

Capabilities:

  • Tertiary education, preferably a degree (B.Com/Business Administration/Project Management/Post Graduate qualification).
  • Confirmed understanding of MS Office.
  • Minimum 1-2 years of relevant project management experience.

Behavioral Dimensions:

  • Solution driven with good communication skills.
  • Good negotiating and conflict resolution skills.
  • Innovative, enforce to Deadline, quality, and is detail oriented.
  • Ability to run and empower people and Lead by example.
  • Maintain personal well-being and balance for self and team.

Kantar is an equal opportunities provider.

Why join Kantar?

We go beyond the obvious, using intelligence, passion and creativity to encourage new thinking and shape the world we live in. We understand more about how people think, feel, shop, share, vote and view than anyone else. Combining our expertise in human understanding with advanced technologies, nobody knows people better than Kantar.

And because we know people, we like to make sure our people are looked after as well. Equality of opportunity for our people are our highest priority, and we encourage our people to work in a way that supports their health and wellbeing. While we encourage our colleagues to spend part of their working week in the office, we understand no one size fits all, and we're flexible in our approach to ensure people feel included and accepted.

We're committed to creating an inclusive culture and value the diversity of our people, clients, suppliers and communities, which is why we welcome applications from all background and sections of society. Even if you feel like you're not a perfect fit, we'd love to receive your application and talk to you about this job or others at Kantar.

Interested?

Send us your application (including CV) today

LI- Hybrid
LI-PO1

Location

Cairo, Downtown MallEgypt

Kantar Rewards Statement

At Kantar we have an integrated way of rewarding our people based around a simple, clear and consistent set of principles. Our approach helps to ensure we are market competitive and also to support a pay for performance culture, where your reward and career progression opportunities are linked to what you deliver.

We go beyond the obvious, using intelligence, passion and creativity to inspire new thinking and shape the world we live in. Apply for a career that's out of the ordinary and join us.

We want to create an equality of opportunity in a fair and supportive working environment where people feel included, accepted and are allowed to flourish in a space where their mental health and well being is taken into consideration.

We want to create a more diverse community to expand our talent pool, be locally representative, drive diversity of thinking and better commercial outcomes.

Kantar is the world's leading data, insights and consulting company. We understand more about how people think, feel, shop, share, vote and view than anyone else. Combining our expertise in human understanding with advanced technologies, Kantar's 30,000 people help the world's leading organisations succeed and grow.

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Project Management Instructor

EGP40000 - EGP120000 Y Smart Investment Solution - SIS

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Job Description

We're Hiring – Project Management Instructor

We're launching a new online learning platform and looking for an experienced Project Management Instructor to deliver a complete diploma program (recorded courses).

Requirements:

Solid professional experience in Project Management

Proven teaching/training background

Strong presentation and communication skills.

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Project Management Officer

EGP900000 - EGP1200000 Y DMS Egypt

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Job Description

We're looking for a proactive and experienced Project Manager to join our team at DMS EGYPT

If you're passionate about leading software development projects, especially in
ERP
or
healthcare
domains, and thrive in dynamic, fast-paced environments — this opportunity is for you.

Qualifications:

  • 15+ years of experience managing
    software development projects
    , preferably in
    ERP
    or
    healthcare systems
    .
  • Solid knowledge of project management methodologies (
    Agile
    ,
    Scrum
    ,
    Waterfall
    ).
  • Strong
    leadership
    ,
    communication
    , and
    problem-solving
    skills.
  • Familiarity with
    ERP platforms
    and/or
    healthcare systems
    is a must.
  • Certifications like
    PMP
    ,
    PRINCE2
    , or
    Agile
    are a strong plus.

About the Role:

  • Lead and manage full project lifecycles – from initiation to closure.
  • Coordinate cross-functional teams and ensure alignment with project goals.
  • Monitor project scope, timelines, budgets, and risks.
  • Ensure high-quality delivery through structured planning and stakeholder communication.
  • Contribute to continuous improvement of project management practices.
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Project Management Officer

EGP600000 - EGP1200000 Y Nok Human Capital

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Job Description

Project Management Officer | Digital Transformation

Join a top-tier S&P 500 technology company that's redefining how millions of customers shop, connect, and grow. We're committed to innovation at scale, fostering a culture of ownership, and delivering world-class products across the globe.

As a PMO Lead within our Engineering Services team, you will own the full lifecycle governance of high-impact engineering and infrastructure programs. From data center expansion to digital tools integration, you will establish and uphold governance frameworks that ensure clarity, accountability, and delivery excellence across all phases of execution.

  • Develop and maintain robust PMO governance structures, including project charters, RAID logs, risk/issue management, and performance dashboards.
  • Lead project planning, resource forecasting, and scheduling activities to align cross-functional teams toward shared goals.
  • Deliver executive-level insights through data-driven reporting (Power BI) and enterprise PMIS tools.
  • Facilitate seamless collaboration across engineering, operations, procurement, and vendor stakeholders.
  • Monitor and ensure compliance with financial, timeline, and quality standards.
  • Champion process innovation, including digital transformation initiatives such as automation, AI dashboards, BIM, and advanced analytics.
  • Drive continuous improvement through structured lessons learned, change management, and knowledge sharing practices.

Required Qualifications

  • Bachelor's degree in Engineering, Management Information Systems, or Project/Construction Management.
  • Minimum 8 years of relevant experience.
  • Demonstrated track record in managing large-scale engineering, infrastructure, or IT programs.
  • Strong background in multinational or cross-border project environments.
  • Expertise in PMO tools, digital project controls, and stakeholder engagement.

What We Offer

  • A high-impact role within a global technology leader.
  • Exposure to complex, enterprise-scale engineering and digital transformation initiatives.
  • Opportunities to innovate with leading-edge tools and scalable processes.
  • Dynamic, collaborative culture focused on performance, inclusion, and growth.
  • Competitive compensation, professional development, and global mobility pathways.

About Us

NOK Human Capital, founded in 2018 as part of NOX Holding, delivers end-to-end HR services across the Middle East and Europe. Backed by NOX's IT, logistics, shipping and financial portfolios, we offer fast, cost-efficient solutions for recruiting and managing talent at all levels. With 300 trusted partners, over 10,000 hires and a 132,000-strong candidate database, we operate in Egypt, Jordan, UAE, KSA, Italy, Germany, Canada and India.

Job Type: Full-time

Application Question(s):

  • Have you worked on engineering or infrastructure projects (e.g., data centers, telecom, or large-scale IT)?
  • Have you worked in a multinational or regional environment with cross-border teams?
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