17 Academic Medicine jobs in the United Arab Emirates

Medical Training Coordinator page is loaded

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Medical Training Coordinator

UAE, Dubai

Job Description

Support the Medical Education activities for HCPs in all field-based medical activities required aiming to achieve company objectives in the region.

Job Responsibilities

• Responsible for managing, designing, developing, coordinating, and conducting all Ax HCP training programs.

• Implementation of Galderma training and medical education strategies

• Coordinate training modules and materials with local Trainers

• Support local congress workshops and participation

• Support the Medical Education, Market access and Sales Team in the implementation of the Product Portfolio Clinical Trials program, Pharmacovigilance and Medical Affairs activities.

• To support governing the ethical practices of all medical activities with the aim to foster the ethical and scientific image of the company as a leading pharmaceutical company.

• Facilitate the implementation of the regional training and medical Education plan

• Support in reviewing professional publications, participating in professional societies, and establishing personal networks.

• Support in planning for the achievement of individual and divisional targets in alignment with the strategies and policies of Galderma.

Minimum Requirements

• Strong medical / pharmaceutical background

• Preferably with a Medical degree or Pharmacy/Biology. Marketing /Project management is advantage.

• More than 5 years Experience in injectable aesthetics market, medical education and Neuro modulators category.

• Minimum 2 years of experience in coordinating medical trainings / medical affairs within the aesthetic Industry.

• Excellent computer skills, including in Microsoft Outlook, Word, Excel, and Power Point

• Strong digital understanding

• Demonstrable experience in Medical Affairs day-to-day duties and responsibilities.

• Previous marketing experience is an advantage

• Good communication skills – including understanding how to clearly communicate messages to consumer and key stakeholders.

• Excellent analytical skills.

• Willingness to learn.

• Interest in trends and new technology.

What we offer in return

• You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

• You will receive a competitive compensation package with bonus structure and extended benefit package.

• You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take accountability.

Next Steps

• Please apply with an English language CV.

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.

• The next step is a virtual conversation with the hiring manager.

• The final step is a panel conversation with the extended team.

Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

About Us

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives, we are advancing dermatology for every skin story.

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About this role

We are seeking a skilled and motivated professional to support medical device implementations and clinical education across the region.

Key responsibilities:

• Conduct hands-on training for healthcare professionals on clinical use of medical diagnostic devices.
• Develop educational resources: workshops, product videos, presentations, and support tools.
• Promote awareness of new medical pathways (e.g. Endocrinology & Bariatric applications).
• Support collaborations with pharmaceutical partners by drafting clinical workflows and co-developing educational initiatives.

Product implementation & support:

• Work with sales and implementation teams to ensure smooth installations and integrations in hospitals, clinics, and private practices.
• Respond to clinical and technical inquiries from healthcare staff ensuring timely resolution.
• Support local trainers and application specialists in regional markets.

Clinical consultation & strategy:

• Gather insights from the field to contribute to product development and clinical strategy.
• Build long-term strategic plans to expand product use in clinical and pharmaceutical environments.

Stakeholder engagement:

• Establish and nurture strong relationships with physicians, nurses, and healthcare administrators.
• Represent the company at medical congresses, industry events, and strategic meetings.

Profile requirements:

• Degree in Nursing, Public Health, Biomedical Engineering, or a related healthcare field (advanced degree preferred).
• Strong clinical background with a deep understanding of medical workflows.
• Experience delivering training in a healthcare or MedTech setting.
• Excellent communication, presentation, and relationship-building skills.
• Ability to work independently in a fast-paced, cross-functional environment.
• Fluent in English and Native Arabic speaker.
• Willingness to travel up to 50% across the region.

Medical Training Coordinator page is loaded

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Medical Training Coordinator

UAE, Dubai

Job Description

Support the Medical Education activities for HCPs in all field-based medical activities required aiming to achieve company objectives in the region.

Job Responsibilities

• Responsible for managing, designing, developing, coordinating, and conducting all Ax HCP training programs.

• Implementation of Galderma training and medical education strategies

• Coordinate training modules and materials with local Trainers

• Support local congress workshops and participation

• Support the Medical Education, Market access and Sales Team in the implementation of the Product Portfolio Clinical Trials program, Pharmacovigilance and Medical Affairs activities.

• To support governing the ethical practices of all medical activities with the aim to foster the ethical and scientific image of the company as a leading pharmaceutical company.

• Facilitate the implementation of the regional training and medical Education plan

• Support in reviewing professional publications, participating in professional societies, and establishing personal networks.

• Support in planning for the achievement of individual and divisional targets in alignment with the strategies and policies of Galderma.

Minimum Requirements

• Strong medical / pharmaceutical background

• Preferably with a Medical degree or Pharmacy/Biology. Marketing /Project management is advantage.

• More than 5 years Experience in injectable aesthetics market, medical education and Neuro modulators category.

• Minimum 2 years of experience in coordinating medical trainings / medical affairs within the aesthetic Industry.

• Excellent computer skills, including in Microsoft Outlook, Word, Excel, and Power Point

• Strong digital understanding

• Demonstrable experience in Medical Affairs day-to-day duties and responsibilities.

• Previous marketing experience is an advantage

• Good communication skills – including understanding how to clearly communicate messages to consumer and key stakeholders.

• Excellent analytical skills.

• Willingness to learn.

• Interest in trends and new technology.

What we offer in return

• You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

• You will receive a competitive compensation package with bonus structure and extended benefit package.

• You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take accountability.

Next Steps

• Please apply with an English language CV.

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.

• The next step is a virtual conversation with the hiring manager.

• The final step is a panel conversation with the extended team.

Our people make a difference

At Galderma, you’ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives, we are advancing dermatology for every skin story.

About Our Team

We are a dynamic organization that specializes in non-invasive diagnostics. Our global presence spans over 100 countries, and we have earned recognition for our patented medical technologies.

Our team is passionate about providing life-changing solutions while fostering a culture of innovation and collaboration.

About the Role

We are seeking a skilled Clinical Specialist to support medical device implementations and clinical education across the region. This role combines technical expertise, clinical training, and strategic support to empower healthcare providers in effectively adopting and using our client's solutions.

Key Responsibilities

• Clinical Education & Training
• Conduct hands-on training for healthcare professionals on the clinical use of medical diagnostic devices.
• Develop educational resources: clinical workshops, product videos, presentations, and support tools.
• Promote awareness of new medical pathways (e.g., Endocrinology & Bariatric applications).
• Support collaborations with pharmaceutical partners by drafting clinical workflows and co-developing educational initiatives.
• Product Implementation & Support
• Work with sales and implementation teams to ensure smooth installations and integrations in hospitals, clinics, and private practices.
• Respond to clinical and technical inquiries from healthcare staff, ensuring timely resolution.
• Support local trainers and application specialists in regional markets.
• Clinical Consultation & Strategy
• Gather insights from the field to contribute to product development and clinical strategy.
• Build long-term strategic plans to expand product use in clinical and pharmaceutical environments.
• Stakeholder Engagement
• Establish and nurture strong relationships with physicians, nurses, and healthcare administrators.
• Represent the company at medical congresses, industry events, and strategic meetings.

Requirements

• Degree in Nursing, Public Health, Biomedical Engineering, or a related healthcare field (advanced degree preferred).
• Strong clinical background with a deep understanding of medical workflows.
• Experience delivering training in healthcare or MedTech settings.
• Excellent communication, presentation, and relationship-building skills.
• Ability to work independently in a fast-paced, cross-functional environment.
• Fluent in English and native Arabic speaker.
• Willingness to travel up to 50% across the region.

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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• 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.

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.

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.