clinical research associate sponsor-dedicated Jobs in Egypt

clinical research associate sponsor-dedicated

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consultant, program management - arc

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regulatory affairs senior associate

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clinical research associate sponsor dedicated

IQVIA

<div>
 
 Job Overview
 
 
 
 Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
 </li>
 <li>
 Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
 </li>
 <li>
 Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
 </li>
 <li>
 Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
 </li>
 <li>
 Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
 </li>
 <li>
 Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
 </li>
 <li>
 Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
 </li>
 <li>
 Collaborate and liaise with study team members for project execution support as appropriate.
 </li>
 <li>
 If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
 </li>
 <li>
 If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 High School Diploma or equivalent Degree in scientific discipline or health care preferred.
 </li>
 <li>
 Requires at least 1 year of on-site monitoring experience.
 </li>
 <li>
 Equivalent combination of education, training and experience may be accepted in lieu of degree.
 </li>
 <li>
 Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
 </li>
 <li>
 Good therapeutic and protocol knowledge as provided in company training.
 </li>
 <li>
 Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
 </li>
 <li>
 Written and verbal communication skills including good command of Arabic and English language.
 </li>
 <li>
 Organizational and problem-solving skills.
 </li>
 <li>
 Effective time and financial management skills.
 </li>
 <li>
 Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
 
 
 </li>
 </ul>
 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
</div>

Clinical Research Associate Sponsor-dedicated

<div>Job Overview 
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.<div>
Essential Functions 
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul></div><div>
Qualifications 
<ul><li>High School Diploma or equivalent Degree in scientific discipline or health care preferred.</li><li>Requires at least 1 year of on-site monitoring experience.</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree.</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of Arabic and English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></div>
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</div>

<div><div><div>New Cairo, Egypt | Full time | Hybrid | R1520390</div></div><div><div> 
Job Overview 
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.</div><div>
Essential Functions 
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.</li><li>Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li><li>Collaborate and liaise with study team members for project execution support as appropriate.</li><li>If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.</li><li>If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.</li></ul></div><div>
Qualifications 
<ul><li>High School Diploma or equivalent Degree in scientific discipline or health care preferred.</li><li>Requires at least 1 year of on-site monitoring experience.</li><li>Equivalent combination of education, training and experience may be accepted in lieu of degree.</li><li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).</li><li>Good therapeutic and protocol knowledge as provided in company training.</li><li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).</li><li>Written and verbal communication skills including good command of Arabic and English language.</li><li>Organizational and problem-solving skills.</li><li>Effective time and financial management skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li></ul></div><div>
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</div></div></div><div></div>

Ray-CRO

Calling Clinical Project Leaders &ndash; EgyptAt RAY-CRO, we don&rsquo;t just execute studies &mdash; we lead them, own them, and deliver real impact.As we expand our regional clinical operations, we are looking for an experienced Clinical Project Leader (CPL) who can:Take full ownership of clinical studies from start to finish Serve as the primary point of contact for sponsors and key stakeholders Lead CRAs and cross-functional teams with confidence and clarity Drive timelines, quality, and compliance across Egypt &amp; KSA Proactively manage risks, decisions, and escalations with accountabilityIf you are someone who: Thinks beyond tasks and focuses on outcomes Thrives in sponsor-facing roles and high-responsibility environments Brings solid CRO or pharma clinical project experienceThis role is made for you.Location: Egypt Apply: careers@ray-cro.comJob Type: Full-time

Clinical Project Lead

Kasrawy Group Careers

Job SummaryThe Project Manager is responsible for leading the planning, execution, and closing of projects, ensuring they are delivered on time, within budget, and to the specified scope and quality. The PM serves as the central point of contact for all project stakeholders, leading a cross-functional team to achieve the defined business objectives.Key ResponsibilitiesA. Project Initiation &amp; Planning<ul><li>Define Scope &amp; Objectives: Work closely with the Project Sponsor and stakeholders to define the project charter, detailed scope, and measurable objectives.</li><li>Develop Project Plan: Create a comprehensive project plan, including the Work Breakdown Structure (WBS), detailed schedule, and resource allocation plan.</li><li>Budget Management: Establish and manage the project budget, tracking expenditure and forecasting financial performance to ensure cost control.</li></ul>B. Project Execution &amp; Leadership<ul><li>Team Leadership: Lead, motivate, and manage the project team, assigning tasks, providing direction, and fostering a collaborative environment.</li><li>Stakeholder Management: Maintain clear, consistent, and proactive communication with all internal and external stakeholders (e.g., clients, vendors, management) to manage expectations and report progress.</li><li>Vendor &amp; Contract Management: Oversee external vendors and contractors, managing contracts and deliverables and ensuring quality adherence.</li></ul>C. Monitoring, Control, &amp; Risk Management<ul><li>Progress Tracking: Monitor and track project progress against the baseline schedule and budget, utilizing project management tools (e.g., MS Project, Jira, Asana).</li><li>Risk &amp; Issue Resolution: Proactively identify potential risks, develop mitigation strategies, and manage a log of all issues to ensure timely resolution and minimize project impact.</li><li>Change Management: Manage changes to the project scope, schedule, or cost using a formal change control process to secure approvals and update the project plan.</li></ul>D. Project Closure<ul><li>Delivery &amp; Sign-off: Ensure all project deliverables are formally accepted by the client/sponsor.</li><li>Documentation: Conduct a final project review, document Lessons Learned, and archive all project documentation for future reference.</li></ul>Required Qualifications &amp; SkillsA. Qualifications (Hard Skills)<ul><li>Education: Bachelors degree in a relevant field (e.g., Business Administration, Engineering, IT, or related field). Masters degree is a plus.</li><li>Experience: 5 years of progressive experience in project management, successfully delivering projects of similar scope and complexity.</li><li>PMP&reg; Certification (Project Management Professional) is required.CAPM&reg; Certification (Certified Associate in Project Management) or Scrum Master (CSM) certification is additional.</li><li>Tool Proficiency: Expertise in project management software (e.g., Microsoft Project, Trello, JIRA, or Primavera P6).</li><li>Methodology: Proven working knowledge of both Waterfall and Agile (Scrum/Kanban) methodologies.</li></ul>Job Type: Full-time

Project Manager

Marc

<div>MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.
MARC is looking to have an experienced candidate for Business Development Specialist
<ul><li>Key responsibilities:</li>
<li>Identify potential clients and collaborators across CRO, pharmaceutical, and biotech sectors.</li>
<li>Conduct market research to map industry trends, competitors, and potential new service areas.</li>
<li>Assist in maintaining an updated database of prospects and outreach activities (CRM support).</li>
<li>Assist in the development of commercial proposals, quotations, and service presentations tailored to client needs.</li>
</ul>
Requirements<ul>
<li>
Bachelor&rsquo;s degree in pharmacy, Biotechnology, Business Administration, or related field.</li>
<li>0&ndash;2 years of experience in business development, sales, marketing, or internship in a CRO, pharma, or life science company.</li>
<li>Familiarity with clinical research services, the CRO business model, or healthcare sector is preferred.</li>
<li>Professional with Digital marketing tools
</li><li>Strong interest in client-facing roles and market growth strategy.</li>
<li>Proficiency in English (written and spoken).</li>
<li>Based in Cairo, Giza, or 6th of October City preferred</li></ul></div>

Business Development Specialist

Work wonders 

Job Title: Business Development Executive / Business Development AssociateCompany: LEO Trading Agency Location: Cairo, Egypt Job Type: Full-TimeAbout Us:LEO Trading Agency is a growing HR services company dedicated to helping businesses attract, retain, and develop top talent. We provide innovative HR solutions, recruitment services, and workforce strategies that drive organizational success.Job Summary:We are seeking a proactive and results-driven Business Development professional to join our team. The ideal candidate will help expand our client base, identify new business opportunities, and promote our HR solutions and services.Key Responsibilities:<ul><li>Identify and pursue new business opportunities in HR services and staffing solutions</li><li>Build and maintain strong relationships with clients, understanding their HR needs</li><li>Present and promote HR services, including recruitment, staffing, and HR consulting</li><li>Conduct market research and stay updated on HR industry trends</li><li>Prepare proposals, presentations, and client reports</li><li>Collaborate with internal HR and operations teams to ensure successful client delivery</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree in Business, HR, Management, or related field</li><li>Strong communication, negotiation, and relationship-building skills</li><li>Self-motivated, proactive, and target-oriented</li><li>Analytical thinking and problem-solving abilities</li><li>Experience in sales, business development, or HR services is a plus</li></ul>What We Offer:<ul><li>Competitive salary with performance-based incentives</li><li>Opportunities for professional growth and career development</li><li>Supportive and dynamic work environment</li></ul>Job Type: Full-timePay: From E&pound;12,000.00 per monthWork Location: Hybrid remote in Heliopolis

Business Developer

Explore 673+ Clinical research associate sponsor dedicated in Egypt this January. Find roles across top companies and apply now to boost your career.

673 clinical research associate sponsor dedicated jobs IN Egypt

Clinical Research Associate Sponsor-dedicated

Clinical Research Associate Sponsor-dedicated

Clinical Research Associate Sponsor-dedicated

Clinical Project Lead

Project Manager

Business Development Specialist

Business Developer