78 Medical Research jobs in the United Arab Emirates

A distinguished molecular entomologist is sought to lead a research team and conduct innovative scientific research in bio-control and crop protection.

The successful candidate will have a proven track record of scholarly productivity and excellence in molecular biology, physiology, and genetics of insect pests.

• Lead a multidisciplinary research team and conduct cutting-edge research in molecular entomology and bio-control.
• Conduct comprehensive research on the biology of insect pests and develop strategies for biological control and genome-editing technologies.
• Publish high-impact findings in peer-reviewed journals and contribute to grant proposals.
• Collaborate with experts from various disciplines and supervise students/postdocs.

• A Ph.D. in entomology or a related field.
• At least 5 years of postgraduate experience.
• Demonstrated expertise in molecular entomology and biocontrol.

• Experience in pest management using molecular, immunological, or protein assays.
• Strong background in biology and ecology of insect pests.

• Advanced knowledge of entomology: rearing, feeding, analysis, and experimentation.
• Ability to work independently and collaborate effectively in multicultural teams.
• Strategic thinking and problem-solving skills.
• Excellent writing and editing skills for publishing in peer-reviewed journals.

This position requires a highly motivated and accomplished scientist who can make significant contributions to the field of molecular entomology.

We are seeking a highly motivated and experienced clinical researcher to lead and execute clinical research initiatives that support the organization's strategic priorities in digital health and telemedicine.

This role requires strong expertise in clinical data analysis, research methodology, biostatistics, and scientific communication, including peer-reviewed publishing and white paper development.

• Design and execute clinical and health services research projects aligned with our mission and strategic goals.
• Lead real-world evidence (RWE) and real-world data (RWD) studies, interpreting results into actionable healthcare insights.
• Develop detailed study protocols, ethical submissions, data collection methodologies, and statistical analysis plans.
• Analyze and interpret complex clinical datasets using statistical tools and visualization platforms.
• Draft, submit, and publish high-quality manuscripts in peer-reviewed journals and develop white papers to support our thought leadership.
• Collaborate with internal stakeholders including data analytics, medical operations, and quality teams to validate research data and findings.
• Monitor emerging trends and literature in digital health, remote patient monitoring, and value-based care to identify and propose new research opportunities.

• Master's degree or PhD in Public Health, Epidemiology, Biostatistics, Health Services Research, Clinical Research, or a related field.
• Minimum of 3–5 years of experience in clinical or health services research, preferably in digital health or telemedicine.
• Proven track record with 10+ publications in peer-reviewed journals and experience authoring white papers.
• Proficiency in statistical analysis software such as SPSS, R, SAS, or STATA, and data visualization tools.
• Strong knowledge of biostatistics, research ethics, and regulatory guidelines.
• Exceptional skills in scientific writing, critical thinking, and data interpretation.
• Demonstrated ability to work both independently and within multidisciplinary teams in a fast-paced, innovative environment.

We are seeking an experienced Equity Research professional to join our team in MENA Healthcare and Consumer Research. As a key member of our research team, you will be responsible for providing thought-leadership to institutional clients on the Healthcare sector.

• Key Responsibilities:
• Collaborate with senior colleagues to provide insights on the Healthcare sector.
• Maintain and update valuation models and databases.
• Prepare materials for regular publication of research reports including data analysis and presentation.
• Contribute to writing research reports including quarterly results alerts stock reports and thematic pieces.
• Communicate with institutional investors and company representatives as well as internal clients.

Requirements:

• A minimum of 3 years of Equity Research experience.
• Strong interest in the Healthcare sector and willingness to specialize in this area.
• Strong modelling skills with ability to forecast.
• Excellent communication skills both verbal and written.
• Team-focused environment where each individual's insight and expertise is valued.
• Analytical approach to building and maintaining financial models.
• Strong numeracy skills.
• Great attention to detail.
• Relationship-building skills.

Benefits:

As a member of our research team, you will have the opportunity to work closely with top-tier analysts, contribute to high-impact research projects, and develop your skills in a collaborative and dynamic environment.

About Us:

We are a leading Global Research franchise with a strong presence in MENA. Our team is dedicated to providing actionable ideas and thematic insights that empower our institutional clients to make informed investment decisions.

Kawader Research Assistant Fellow Job Opportunity

• This position offers a unique chance to be part of an innovative research project focused on the molecular structure and function of eumelanin, utilizing solid-state NMR spectroscopy and other analytical techniques.

IROS CRO Abu Dhabi Emirate, United Arab Emirates

IROS CRO Abu Dhabi Emirate, United Arab Emirates. IROS is a leading Contract Research Organisation (CRO) in the Middle East, specializing in clinical trials across diverse therapeutic areas and integrating real-world data. We are seeking a highly qualified Clinical Research Associate (CRA) to join our team and play a key role in advancing clinical research excellence.

As a Clinical Research Associate, you will be responsible for supporting clinical trial operations from study start-up through to close-out. You will collaborate with study sites, sponsors, and internal teams to ensure compliance, data integrity, and adherence to international standards of Good Clinical Practice (GCP).

• Conduct feasibility studies and site qualification assessments.
• Support study setup, including regulatory submissions and documentation.
• Manage regulatory compliance and maintain essential study records.
• Perform monitoring visits, review protocol deviations, and report adverse events.
• Ensure data integrity and adherence to GCP.
• Provide timely updates to clients and internal stakeholders.
• Oversee study site closure and final documentation.

Education:

• Bachelor’s degree in Life Sciences.

Experience:

• 4–6 years in clinical research, with direct involvement in at least five interventional clinical trials.

Skills & Knowledge:

• Strong organizational, decision-making, and time management skills.
• Excellent communication and collaboration abilities, particularly in cross-cultural environments.
• Proficiency in Microsoft Office applications.
• Certification in Good Clinical Practice (GCP).
• Demonstrated ability to lead, document thoroughly, and work effectively in a matrixed structure.

• Associate

• Full-time

• Research

• Research Services

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The job holder is responsible to coordinate and conduct clinical research trials, ensuring the safety and well-being of study participants while maintaining the integrity of study data. This role involves direct patient care, data collection, and collaboration with multidisciplinary teams in clinical facilities and clinical trial units.

Core Responsibilities

Clinical Trial Coordination:

• Assist in the execution of clinical trial protocols, including the identification of eligibility criteria and setting up study procedures.

• Recruit and screen potential study participants, obtain informed consent, and assess eligibility based on study criteria.

• Provide comprehensive nursing care to study participants, including monitoring vital signs, administering medications, and managing study-related interventions.

• Collect, record, and maintain accurate patient data according to study protocols and regulatory requirements, ensuring data integrity and confidentiality.

• Coordinate the collection, processing, and shipment of biological samples as required by the study protocol.

Compliance and Regulatory:

• Ensure adherence to clinical trial protocols and regulatory requirements, including Good Clinical Practice (GCP) guidelines.

• Maintain thorough and accurate documentation of all study-related activities, including patient interactions, data collection, and adverse event reporting.

• Prepare for and support internal and external audits by maintaining organized and compliant study records.

Communication and Collaboration:

• Serve as the primary contact for study participants, answering questions and addressing concerns throughout the trial period.

• Collaborate with principal investigators, research staff, and clinicians to ensure the successful execution and completion of clinical trials.

Patient Education and Support:

• Educate study participants and their families about the clinical trial process, study procedures, and potential risks and benefits.

• Provide emotional and psychological support to participants, ensuring a patient-centered approach and addressing any concerns.

Quality Assurance:

• Monitor adherence to study protocols, ensuring compliance with regulatory standards and institutional policies.

• Identify areas for process improvement to enhance study quality and efficiency.

Training and Mentorship:

• Train and mentor research staff in clinical trial procedures and best practices.

• Participate in educational sessions and seminars to stay current with developments in clinical research and nursing practices.

Educational Requirements:

• Master's degree in nursing (MSN) or related advanced program.

• Bachelor's degree in nursing (BSN).

• Licensed to practice nursing and able to perform basic procedures including collecting, handling and processing samples

Overall Experience:

• Minimum of 2 years of clinical nursing experience and clinical research or clinical trial nursing, preferably within research institution or hospital setting.

• Direct clinical care experience, including patient assessment, medication administration, and monitoring.

• Experience with clinical research protocols, patient recruitment, data collection, and regulatory compliance.

• Knowledge of GCP guidelines and experience with IRB submissions and clinical trial auditing.

• Seniority level Not Applicable

• Employment type Full-time

• Job function Other
• Industries Hospitals and Health Care

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Dubai, Dubai, United Arab Emirates 19 hours ago

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Get AI-powered advice on this job and more exclusive features.

The job holder is responsible to coordinate and conduct clinical research trials, ensuring the safety and well-being of study participants while maintaining the integrity of study data. This role involves direct patient care, data collection, and collaboration with multidisciplinary teams in clinical facilities and clinical trial units.

Core Responsibilities

Clinical Trial Coordination:

• Assist in the execution of clinical trial protocols, including the identification of eligibility criteria and setting up study procedures.

• Recruit and screen potential study participants, obtain informed consent, and assess eligibility based on study criteria.

• Provide comprehensive nursing care to study participants, including monitoring vital signs, administering medications, and managing study-related interventions.

• Collect, record, and maintain accurate patient data according to study protocols and regulatory requirements, ensuring data integrity and confidentiality.

• Coordinate the collection, processing, and shipment of biological samples as required by the study protocol.

Compliance and Regulatory:

• Ensure adherence to clinical trial protocols and regulatory requirements, including Good Clinical Practice (GCP) guidelines.

• Maintain thorough and accurate documentation of all study-related activities, including patient interactions, data collection, and adverse event reporting.

• Prepare for and support internal and external audits by maintaining organized and compliant study records.

Communication and Collaboration:

• Serve as the primary contact for study participants, answering questions and addressing concerns throughout the trial period.

• Collaborate with principal investigators, research staff, and clinicians to ensure the successful execution and completion of clinical trials.

Patient Education and Support:

• Educate study participants and their families about the clinical trial process, study procedures, and potential risks and benefits.

• Provide emotional and psychological support to participants, ensuring a patient-centered approach and addressing any concerns.

Quality Assurance:

• Monitor adherence to study protocols, ensuring compliance with regulatory standards and institutional policies.

• Identify areas for process improvement to enhance study quality and efficiency.

Training and Mentorship:

• Train and mentor research staff in clinical trial procedures and best practices.

• Participate in educational sessions and seminars to stay current with developments in clinical research and nursing practices.

Educational Requirements:

• Master’s degree in nursing (MSN) or related advanced program.

• Bachelor’s degree in nursing (BSN).

• Licensed to practice nursing and able to perform basic procedures including collecting, handling and processing samples

Overall Experience:

• Minimum of 2 years of clinical nursing experience and clinical research or clinical trial nursing, preferably within research institution or hospital setting.

• Direct clinical care experience, including patient assessment, medication administration, and monitoring.

• Experience with clinical research protocols, patient recruitment, data collection, and regulatory compliance.

• Knowledge of GCP guidelines and experience with IRB submissions and clinical trial auditing.

• Seniority levelNot Applicable

• Employment typeFull-time

• Job functionOther
• IndustriesHospitals and Health Care

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Dubai, Dubai, United Arab Emirates 19 hours ago

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As a skilled professional in clinical research nursing, you will play a vital role in ensuring the safety and well-being of patients while maintaining the integrity of study data.

The job holder is responsible for coordinating and conducting clinical research trials, involving direct patient care, data collection, and collaboration with multidisciplinary teams in clinical facilities and clinical trial units.

Clinical Trial Coordination:

• Assist in executing clinical trial protocols, including identifying eligibility criteria and setting up study procedures.
• Recruit and screen potential study participants, obtain informed consent, and assess eligibility based on study criteria.
• Provide comprehensive nursing care to study participants, including monitoring vital signs, administering medications, and managing study-related interventions.
• Collect, record, and maintain accurate patient data according to study protocols and regulatory requirements, ensuring data integrity and confidentiality.
• Coordinate the collection, processing, and shipment of biological samples as required by the study protocol.

Compliance and Regulatory:

• Ensure adherence to clinical trial protocols and regulatory requirements, including Good Clinical Practice (GCP) guidelines.
• Maintain thorough and accurate documentation of all study-related activities, including patient interactions, data collection, and adverse event reporting.
• Prepare for and support internal and external audits by maintaining organized and compliant study records.

Communication and Collaboration:

• Serve as the primary contact for study participants, answering questions and addressing concerns throughout the trial period.
• Collaborate with principal investigators, research staff, and clinicians to ensure the successful execution and completion of clinical trials.

Patient Education and Support:

• Educate study participants and their families about the clinical trial process, study procedures, and potential risks and benefits.
• Provide emotional and psychological support to participants, ensuring a patient-centered approach and addressing any concerns.

Quality Assurance:

• Monitor adherence to study protocols, ensuring compliance with regulatory standards and institutional policies.
• Identify areas for process improvement to enhance study quality and efficiency.

Training and Mentorship:

• Train and mentor research staff in clinical trial procedures and best practices.
• Participate in educational sessions and seminars to stay current with developments in clinical research and nursing practices.

Required Skills and Qualifications:

• Bachelor's degree in nursing (BSN).
• Licensed to practice nursing and able to perform basic procedures including collecting, handling and processing samples
• Minimum of 2 years of clinical nursing experience and clinical research or clinical trial nursing, preferably within research institution or hospital setting.

Benefits:

This role offers opportunities for growth and development in a dynamic environment. You will have the chance to work with a talented team of professionals and contribute to the advancement of medical knowledge.

Others:

Please note that this is a full-time position. If you are a motivated and dedicated individual who is passionate about clinical research nursing, we encourage you to apply.

A clinical research coordinator with nursing background is needed to manage and participate in all phases of the research process. The role involves supporting professional nursing practice across practice settings and the continuum of care to meet the needs of the research participant and family.

The nurse will be accountable for advocating human subject rights and coordinating participant/family education in the clinical research setting. Work is primarily self-directed with guidance from staff physicians and/or principal investigators.

• Collects and reviews health data in a comprehensive and systematic format by assessing, observing, and evaluating a patient/family based on established guidelines and protocols.
• Assesses patient/family educational needs and readiness to learn, considering age-related factors and using appropriate resources.
• Uses communication techniques appropriate to the patient/family's age and abilities.
• Interprets assessment data to reflect the patient's status and documents relevant data in a retrievable form.
• Develops and documents the plan of care, including continuity of care with the patient, family, and health team members.
• Implements the plan of care in collaboration with the health care team and conducts patient and family teaching consistently.
• Performs treatments and procedures according to research protocol guidelines and maintains a safe, clean, and organized environment.
• Applies asepsis and infection control principles; documents actions, outcomes, and future plans.
• Provides ongoing evaluation of patient progress toward research outcomes and involves the patient, family, and health care team in the evaluation process.
• Makes ethical decisions and acts as a patient advocate, respecting privacy, dignity, personal preferences, and culture.
• Reviews protocol, develops budget justifications, determines feasibility, and interfaces with investigators and sponsors to initiate protocol and draft budgets.
• Develops and conducts training for staff responsible for non-nursing protocol procedures and participates in study meetings as required.
• Develops effective screening tools and patient eligibility processes and coordinates recruitment activities according to approved procedures.
• Ensures protocol compliance, reports adverse events to IRB and principal investigator/sponsor, and maintains accurate documentation and drug/device accountability as required.

• Required: Bachelor's degree in nursing from an accredited program; current Registered Nurse (RN) license; Basic Life Support (BLS) competency; minimum of two years RN experience in ambulatory and/or acute care settings.
• Desirable: Certification from an accredited body (e.g., ACRP or SOCRA) is strongly preferred.
• Required: Extensive knowledge of research study design, development, disease processes, and at least three years of related research experience in a healthcare institution; at least four years of experience as a registered nurse.
• Desirable: More than five years of experience in clinical research and conducting clinical trials.

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Health Care Provider
• Industries: Hospitals and Health Care