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clinical research associate

Ray-CRO

<p>Clinical Research Associate (CRA) Opportunity &ndash; Saudi Arabia</p><p>RAY-CRO is expanding its operations in Saudi Arabia and is seeking a qualified Clinical Research Associate (CRA) to support regional clinical research activities and contribute to high-quality study execution.</p><p>The successful candidate will be responsible for:</p><ul><li>End-to-end site management from initiation through close-out</li><li>Ensuring compliance with ICH-GCP, study protocols, and applicable regulatory requirements</li><li>Effective communication with investigative sites, sponsors, and internal teams</li><li>Proactive issue identification and resolution</li><li>Maintaining high standards of quality, timelines, and patient safety</li></ul><p>Location: KSA<br/>Applications: careers@ray-cro.com</p><p>This is an excellent opportunity to join a regional CRO with an expanding clinical research footprint in Saudi Arabia.</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

Clinical Research Associate

IQVIA

<div><p><b>Job Overview</b><br>
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.</p><p></p><div><b>
Essential Functions</b><br>
<ul><li>Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.</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><p></p><div><b>
Qualifications</b><br>
<ul><li>High School Diploma or equivalent Degree in scientific discipline or health care preferred.</li><li>Requires at least 2 years of 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.</li><li>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><p></p><p>
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</p></div>

Experienced Clinical Research Associate Sponsor-dedicated

<div><div><div>Riyadh, Saudi Arabia | Full time | Hybrid | R1508170</div></div><p></p><div><div><b><br>
Job Overview</b><br>
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.<br>
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<b>Essential Functions</b><br>
<ul><li>Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.</li><li>Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.</li><li>Assist with periodic review of study files for completeness.</li><li>Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.</li><li>Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.</li><li>May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.</li><li>May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.</li></ul><br>
<b>
Qualifications</b><br>
<ul><li>High School Diploma or equivalent Req</li><li>At least 1 year experience as CTA with Finance responsibilities</li></ul></div><ul><li>Experience in contracts, payments, budgeting, invoicing</li><li>Equivalent combination of education, training and experience.</li><li>Minimum one year clinical research experience strongly preferred.</li><li>Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.</li><li>Written and verbal communication skills including good command of Arabic and English language.</li><li>Effective time management and organizational skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li><li>Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.</li><li>Knowledge of applicable protocol requirements as provided in company training.</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></div>

Clinical Trials Assistant with Finance Responsibilities Sponsor-dedicated

Coloplast

<div>
 At Coloplast, we are dedicated to making life easier for people with intimate healthcare needs. We are looking for passionate individuals to join our team and contribute to our mission.
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 Coloplast is one of the world&rsquo;s leading suppliers of healthcare products and services, specializing in ostomy care, continence care, wound &amp; skin care, and urology care.
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 Our mission is to make life easier for people with intimate healthcare needs. This requires both an understanding of their medical challenges and the many other concerns that impact their lives. These can be related to social situations, travel, work, intimacy, exercise or just a trip to the shops. We gain this understanding by listening to them and to nurses and specialists who care for them. It is what inspires us and enables us to deliver the products and services that can make a difference.
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  Position Overview
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 We are seeking a motivated Associate Clinical Manager to support Coloplast&rsquo;s clinical agenda across Saudi Arabia and the UAE in the fields of ostomy care and continence care. The role combines clinical education, research support, cross-functional collaboration, and field-based activities, requiring frequent travel within the region. The successful candidate will play a vital role in advancing patient care, supporting healthcare professionals, and enabling the company&rsquo;s mission of making life easier for people with intimate healthcare needs.
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  Key Responsibilities
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  Clinical Education &amp; Support
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   Deliver training and education programs to nurses, physicians, and other healthcare professionals on Coloplast&rsquo;s ostomy and continence care portfolios and tools.
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   Provide clinical support during patient care activities, including bedside and outpatient settings, to optimize outcomes and reduce complications.
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   Demonstrate strong presentation and facilitation skills during workshops, hospital sessions, and conferences.
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  Research &amp; Evidence Generation
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   Support ongoing clinical studies, surveys, and real-world evidence projects in ostomy and continence care.
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   Assist in data collection, analysis, and dissemination of clinical insights.
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   Collaborate with internal and external stakeholders to identify gaps in clinical practice and contribute to research publications and advisory board initiatives.
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  Cross-Functional Collaboration
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   Work closely with sales, marketing, and Care-Consumer Support teams to ensure alignment of clinical messages with business priorities.
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   Provide clinical input to marketing campaigns, educational materials, and patient support programs.
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   Support sales colleagues with clinical expertise during customer field visits.
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  Product Expertise &amp; Case Support
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   Develop deep knowledge of Coloplast&rsquo;s product portfolio and competitive landscape.
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   Provide in-field support for product trials, case coverage, and troubleshooting in both surgical and outpatient settings.
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   Offer technical and clinical guidance to healthcare providers to ensure correct product adoption.
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  Market Insight &amp; Development
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   Monitor clinical trends, healthcare regulations, and competitive activities in Saudi Arabia and UAE.
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   Share market insights with internal stakeholders to shape strategy, innovation, and service models.
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   Contribute to initiatives that establish clinical centers of excellence, nurse education programs, and new care pathways.
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  Compliance &amp; Quality
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   Uphold the highest standards of patient safety, ethical conduct, and compliance with hospital protocols and local regulations.
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   Ensure all activities align with Coloplast&rsquo;s global compliance framework and healthcare facility requirements.
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  Qualifications
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   Bachelor&rsquo;s degree in Medicine, Health Education, Nursing or a related healthcare discipline (Master&rsquo;s degree in Public Health, Healthcare Quality, or Medical Research preferred).
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   1&ndash;3 years of clinical experience in colorectal field, urology field, ostomy care, continence care, wound care, or surgical specialties.
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   Strong presentation and communication skills with the ability to engage diverse healthcare audiences.
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   Experience or interest in clinical research, data analysis, and publication support.
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   Ability to collaborate with marketing, sales, and clinical teams to execute integrated projects.
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   Flexible and willing to travel within Saudi Arabia and the UAE.
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   Fluency in English required; Arabic preferred.
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  What We Offer
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   Purpose-Driven Work At Coloplast, our mission is to make life easier for people with intimate healthcare needs. Your work will have a meaningful impact on our users' lives.
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   Collaborative Culture We believe in closeness &ndash; to our customers and to each other. Our open and honest dialogue fosters a supportive and inclusive environment.
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   Passion for Innovation We are driven by a passion to make a difference. This motivates us to find new ways to improve and innovate, ensuring we bring the best solutions to those who need them.
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   Respect and Responsibility We respect each other and the world around us. Integrity and honesty are at the heart of everything we do, ensuring we act responsibly in all our endeavours.
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  Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16.000 people and with products available in more than 143 countries, we are one of the world&acute;s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward &ndash; we explore, learn and look for new ways of doing things.
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  Coloplast is committed to being an inclusive organization, where people bring their differences to work each day, fulfil their potential and have a strong sense of belonging because &ndash; and not despite &ndash; of their differences. We therefore encourage all qualified candidates to apply regardless of gender, age, race, nationality, ethnicity, sexual orientation, religious belief or physical ability.
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  Visit us on Coloplast.com.
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  Watch the film. Follow us on LinkedIn. Like us on Facebook.
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Associate Clinical Manager - OC & CC (KSA & UAE)

Alfaisal University

<div><div><div><h3 class="jobSectionHeader"><b>Associate Professor of Epidemiology (CoM#171225)</b></h3><div><ul><li>College of Medicine (CoM)</li>
</ul></div></div></div><div><h4 class="jobSectionHeader"><b>Job Title</b></h4>
<p>Associate Professor of Epidemiology
</p><h4 class="jobSectionHeader"><b>Background</b></h4>
<p>Alfaisal University College of Medicine invites applications for a full-time Associate Professor of Epidemiology in the Department of Biostatistics, Epidemiology &amp; Public Health. This senior academic role will support the expansion of research programs, MPH and PhD tracks, and national collaborations aligned with Vision 2030 health transformation priorities.</p>
<p>We seek a scholar with a strong record of research excellence in epidemiologic methods, chronic disease epidemiology, lifestyle and behavioral epidemiology, digital health surveillance, infectious disease modeling, environmental/occupational epidemiology, or health services research. Candidates should demonstrate a robust track record of competitive grant funding, interdisciplinary collaborations, and leadership in graduate education.</p>
<p>The successful candidate will join a rapidly growing academic environment with active institutional partnerships across Saudi Arabia&mdash;including public health authorities, healthcare clusters, national registries, and digital health platforms. The role includes teaching, supervising thesis research, leading funded projects, mentoring junior faculty, and contributing to departmental and university development.</p>
<h4 class="jobSectionHeader"><b>Job Description</b></h4>
<ul><li>Teach epidemiology and public health courses at the undergraduate, MPH, and PhD levels.</li>
<li>Lead research projects and contribute to national and international collaborations.</li>
<li>Supervise MSc, MPH, and PhD theses, and mentor junior faculty and postdoctoral researchers.</li>
<li>Conduct independent, high-impact epidemiologic research aligned with institutional and national priorities.</li>
<li>Develop advanced methodologies for population health, disease surveillance, causal inference, and public health analytics.</li>
<li>Publish in high-impact journals and participate in grant writing and funded research initiatives.</li>
<li>Contribute to curriculum development, accreditation, and academic governance.</li>
<li>Support community engagement, professional training, and capacity-building initiatives.</li>
<li>Participate in departmental.</li>
</ul><h4 class="jobSectionHeader"><b>Job Type</b></h4>
<ul><li>Full Time Faculty Member</li>
</ul><h4 class="jobSectionHeader"><b>Discipline</b></h4>
<ul><li>Department of Biostatistics, Epidemiology &amp; Public Health<br>
College of Medicine, Alfaisal University<br>
Riyadh, Saudi Arabia
</li></ul><h4 class="jobSectionHeader"><b>Preffered Qualification
</b></h4><ul><li>PhD in Epidemiology or a closely related field.</li>
<li>Minimum of 5&ndash;7 years of academic experience post-PhD, with evidence supporting appointment at the Associate Professor rank.</li>
<li>Strong publication record in Q1 journals, with demonstrated leadership in epidemiologic research.</li>
<li>Experience in designing and leading large-scale epidemiologic studies, surveillance systems, or health assessments.</li>
<li>Proficiency in epidemiologic software and statistical packages (R, STATA, SAS, Python).</li>
<li>Demonstrated excellence in teaching, supervision, and mentorship at graduate levels.</li>
<li>Experience collaborating with national health authorities, research centers, or healthcare systems.</li>
<li>Track record of securing competitive grants and leading funded public health projects.</li>
<li>Expertise in digital health, real-time surveillance, or advanced epidemiologic modeling.</li>
<li>Experience contributing to the development of MPH, PhD, or professional training programs.</li>
<li>Experience in academic leadership roles (program director, committee chair, research lead).</li>
<li>Qualification from the western accredited universities will be preferred.</li>
</ul><br>
<b>Please upload CV in ENGLISH ONLY</b></div></div><p></p>

Associate Professor of Epidemiology

<div><div><div><h3 class="jobSectionHeader"><b>Assistant Professor of Biostatistics (CoM#171225)</b></h3><div><ul><li>College of Medicine (CoM)</li>
</ul></div></div></div><div><h4 class="jobSectionHeader"><b>Job Title</b></h4>
<p>Assistant Professor of Biostatistics</p>
<h4 class="jobSectionHeader"><b>Background</b></h4>
<p>Alfaisal University College of Medicine invites applications for a full-time Assistant Professor of Biostatistics in the Department of Biostatistics, Epidemiology &amp; Public Health. This position supports the College&rsquo;s expanding research enterprise, MPH program, PhD tracks, and ongoing collaborations with national partners in health policy, epidemiology, and digital health.</p>
<p>We seek a candidate with strong expertise in advanced statistical analysis and modeling, epidemiological methods, causal inference, survival analysis, machine learning applications in healthcare, and the design/analysis of clinical and population-based studies.
</p><p>Scholars whose research aligns with noncommunicable diseases, health services research, digital health analytics, lifestyle epidemiology, or national surveillance systems are strongly encouraged to apply.</p>
<p>The successful candidate will join a dynamic academic environment with active collaborations across Saudi Arabia, the GCC, and international institutions. The role includes teaching, supervising graduate students, leading methodological research, and contributing to departmental and institutional growth in biostatistics and public health analytics.</p>
<h4 class="jobSectionHeader"><b>Job Description</b></h4>
<ul><li>Teach biostatistics and quantitative methods at the undergraduate and graduate levels.</li>
<li>Contribute to curriculum development for MPH, MBBS, and PhD programs.</li>
<li>Conduct independent research in applied and theoretical biostatistics, epidemiologic modeling, or health data science.</li>
<li>Support faculty and students through statistical consultation and research design guidance.</li>
<li>Supervise MSc, MPH, and PhD theses involving quantitative and statistical methodologies.</li>
<li>Publish in peer-reviewed journals and contribute to collaborative, grant-funded research.</li>
<li>Participate in departmental, college, and university service and accreditation activities.</li>
</ul><h4 class="jobSectionHeader"><b>Job Type</b></h4>
<ul><li>Full Time Faculty Member</li>
</ul><h4 class="jobSectionHeader"><b>Discipline</b></h4>
<ul><li>Department of Biostatistics, Epidemiology &amp; Public Health<br>
College of Medicine, Alfaisal University<br>
Riyadh, Saudi Arabia
</li></ul><h4 class="jobSectionHeader"><b>Preffered Qualification
</b></h4><ul><li>PhD in Biostatistics, Statistics, Epidemiology (with advanced quantitative focus), or equivalent.
</li><li>Minimum 2-3 years of experience in a university</li>
<li>Strong record of peer-reviewed publications, preferably in Q1 journals.</li>
<li>Demonstrated expertise in regression modeling, longitudinal data analysis, survival analysis, causal inference, multilevel models, and statistical programming.</li>
<li>Proficiency in SPSS, R, STATA, SAS, Python, or similar statistical platforms.</li>
<li>Evidence of teaching effectiveness and mentorship at the undergraduate or graduate level.</li>
<li>Experience in Bayesian statistics, machine learning, or predictive analytics.</li>
<li>Experience collaborating on public health, clinical, or population-based research.</li>
<li>Experience supervising graduate research or contributing to academic program development.</li>
<li>Experience contributing to national surveys, lifestyle surveillance systems, or health policy analytics.</li>
<li>Qualification from the western accredited universities will be preferred.</li>
</ul><br>
<b>Please upload CV in ENGLISH ONLY</b></div></div><p></p>

Assistant Professor of Biostatistics

Novartis

<div>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 The primary responsibility of this role is to plan, develop, design and execute Real World Evidence (RWE) studies in Saudi Arabia to develop and demonstrate the value of Novartis marketed and pipeline products to payers and clinicians across different therapeutic areas.
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  About The Role
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 </strong>
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  Major Accountabilities:
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   Design and implement innovative Real-World Evidence (RWE) programs to address drug development challenges, support regulatory decisions (e.g., label changes, new indications), and enable payer decision-making for reimbursement success.
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   Lead implementation research initiatives, including population health models, to drive adoption of Novartis innovations aligned with patient and healthcare system needs.
  </li>
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   Map and license Real World Data (RWD) sources, build research collaborations, and execute RWE projects in close partnership with cross-functional teams.
  </li>
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   Develop and integrate RWE strategies into product/disease area plans and launch strategies, ensuring alignment with global and local evidence plans.
  </li>
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   Support integrated evidence planning, cost-effectiveness modeling, and external HEOR partnerships to strengthen access and reimbursement efforts.
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   Manage collaborations with investigators, KOLs, vendors, and external stakeholders to co-design innovative study designs and ensure quality delivery of research projects.
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   Communicate scientifically valid RWE to stakeholders (HCPs, payers, regulators) and lead internal training on advanced RWE methodologies and implementation science.
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  Minimum Requirements
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   A degree as Medical Doctor (MD) or PharmD or PhD. Also, if they have a master's degree in health science and/or master's in Evidence Generations / Clinical Research.
  </li>
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   Languages: Fluent in English (oral and written), Arabic (native) is preferable.
  </li>
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   Minimum 3+ years of experience in conducting RWE research for pharmaceutical products within pharma, CROs, or academic institutions; or in a closely related discipline (e.g., clinical research, statistics, epidemiology, pricing).
  </li>
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   Strong understanding of Medical Affairs, Drug Development, Market Access/HEOR, Safety, or related areas to generate value evidence from both retrospective and prospective studies.
  </li>
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   Good Understanding of Saudi Arabia market research landscape.
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 <strong>
  Why Novartis:
 </strong>
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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  Benefits and Rewards:
 </strong>
 Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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Evidence Generation Head

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