14 Clinical Dermatology jobs in the United Arab Emirates

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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 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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• 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.

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 level Not Applicable

• Employment type Full-time

• Job function Other
• Industries Hospitals and Health Care

Referrals increase your chances of interviewing at Dubai Health by 2x

Dubai, Dubai, United Arab Emirates 19 hours ago

We're unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Clinical research professionals play a pivotal role in the success of clinical trials. Their responsibilities include ensuring that studies are conducted according to Good Clinical Practice (GCP) guidelines and regulations.

Key aspects of their job include conducting feasibility studies and site qualification assessments to determine whether a study can be successfully implemented at a particular site.

The ideal candidate will have a thorough understanding of clinical research principles, including GCP and International Conference on Harmonisation (ICH) guidelines.

In this role, you will be responsible for:

• Conducting feasibility studies and site qualification assessments to identify potential sites for clinical trials
• Supporting study setup, including regulatory submissions and documentation
• Managing regulatory compliance and maintaining essential study records
• Performing monitoring visits, reviewing protocol deviations, and reporting adverse events
• Ensuring data integrity and adherence to GCP guidelines

To succeed in this position, you will need:

• A Bachelor's degree in Life Sciences or a related field
• 4-6 years of experience in clinical research, with direct involvement in at least five interventional clinical trials
• 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)

We seek a highly motivated and organized individual who is passionate about clinical research and has a strong desire to work in a dynamic and fast-paced environment.

Senior CRA Job Opportunity

We are seeking a highly skilled Senior Clinical Research Associate to join our team. As a Senior CRA, you will be responsible for ensuring the smooth execution of clinical trials and maintaining compliance with regulatory requirements.

The ideal candidate will have extensive experience in clinical research, preferably in a senior CRA role, and possess comprehensive knowledge of ICH-GCP guidelines and regulatory requirements.

Key Responsibilities

• Trial Management: Coordinate and lead all aspects of clinical trials to ensure flawless execution and compliance with regulatory requirements.
• Study Site Monitoring: Monitor study sites to ensure accurate data collection and adherence to study protocols.
• Feasibility and Startup Activities: Support different aspects of feasibility and startup activities, including tracking RFPs, site identification, EC/RA submissions, contract/budget negotiations.
• Cross-Functional Collaboration: Collaborate with cross-functional teams to successfully implement study plans and resolve any issues that arise.
• Documentation and Record Keeping: Maintain all documentation and records according to company and regulatory standards.
• Mentorship and Training: Provide guidance and mentorship to junior CRAs, encouraging a culture of inclusion and continuous improvement.

Requirements

• Experience: Proven experience in clinical research, preferably in a senior CRA role.
• Knowledge: Comprehensive knowledge of ICH-GCP guidelines and regulatory requirements.
• Skills: Strong analytical skills and attention to detail, excellent communication and organizational skills, ability to work independently and as part of a collaborative team.
• Languages: Fluency in Arabic and English language.

About the Role

This is a full-time position with a standard work schedule. The successful candidate will be based in the United Arab Emirates and will be part of an outstanding team.

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

Registered Nurse - Clinical Research Coordinator (RN-CRC) role at Sheikh Shakhbout Medical City - SSMC. The RN-CRC is accountable for managing and/or participating in all phases of the research process, supports professional nursing practice across practice settings and the continuum of care to meet the needs of the research participant and family, advocates for human subject rights, and coordinates participant/family education in the clinical research setting. Work is primarily self-directed with guidance from staff physicians and/or principal investigators. The RN-CRC participates in organizing and monitoring protocols, staff education in protocol areas, and coordinates study data collection, storage, retrieval, and related procedures to comply with local and international regulatory laws and institutional guidelines.

• 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

A Specialist Dermatologist plays a pivotal role in diagnosing, treating, and managing skin conditions and disorders. They provide specialized care and consultations to patients. With their knowledge and expertise, they evaluate symptoms, conduct examinations and biopsies, prescribe treatment plans, and perform non-invasive procedures when required.

• Conduct comprehensive dermatological assessments to diagnose various skin conditions.
• Manage patient history and document case notes for ongoing care.
• Develop individualized treatment plans addressing patient-specific needs.
• Perform diagnostic tests, such as skin biopsies and patch tests effectively.
• Educate patients on preventing skin conditions and skincare routines.

Responsibilities also include collaborating with medical professionals, staying informed about advancements in dermatology practices, performing cosmetic procedures, providing prompt treatment for emergencies, and handling laboratory work related to skin samples and results. The Specialist Dermatologist participates in research to improve patient care standards.

To excel in this role, you will require:

• A Doctor of Medicine (MD) degree for practice.
• Board certification in Dermatology from a recognized medical board.
• A valid license to practice dermatology in the UAE.
• Proven experience working as a specialized dermatologist in a clinical setting.
• Keen clinical acumen and adept diagnosis skills.
• Superior communication skills for patient education and collaboration.

Role Description:

We are seeking an experienced Aesthetic General Practitioner with DHA and UAE certification to join our esteemed clinic. The ideal candidate will have a strong background in delivering top-quality care to diverse patient bases.