11 Academic Medicine jobs in the United Arab Emirates

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

Job Responsibilities

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

Implement Galderma training and medical education strategies.

Coordinate training modules and materials with local Trainers.

Support local congress workshops and participation

Assist the Medical Education, Market Access, and Sales Teams in implementing the Product Portfolio Clinical Trials program, Pharmacovigilance, and Medical Affairs activities.

Ensure ethical practices in all medical activities to foster the ethical and scientific image of the company.

Facilitate the implementation of regional training and medical education plans.

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

Assist in planning for achieving individual and divisional targets aligned with Galderma's strategies and policies.

Qualifications

• Strong medical/pharmaceutical background; preferably with a Medical degree or Pharmacy/Biology. Marketing or Project Management experience is an advantage.
• Over 5 years of experience in the injectable aesthetics market, medical education, and Neuro modulators category.
• At least 2 years of experience coordinating medical trainings or medical affairs within the aesthetic industry.
• Excellent computer skills, including Microsoft Outlook, Word, Excel, and PowerPoint.
• Demonstrable experience in Medical Affairs duties and responsibilities.
• Previous marketing experience is an advantage.
• Good communication skills to clearly convey messages to consumers and stakeholders.
• Excellent analytical skills and willingness to learn.
• Interest in trends and new technology.

What we offer in return

• Work in an organization that values diversity and inclusion, believing it leads to better outcomes.
• Competitive compensation package with bonus and extended benefits.
• Opportunity to grow in a company that encourages ownership and accountability from day one.

Next Steps

Please apply with an English language CV. If your profile matches, you will be invited for a virtual initial conversation with the recruiter, followed by a discussion with the hiring manager, and finally a panel interview with the extended team.

Our people make a difference

At Galderma, we value the unique contributions of every team member. We foster professionalism, collaboration, and a friendly, supportive environment for everyone to thrive.

Deliver impactful training programs on aesthetic dermatology products and medical devices.

• Develop and implement comprehensive training initiatives.
• Lead trainings on aesthetic dermatology products and medical devices.

Requirements:

• Strong background in aesthetic dermatology products and medical devices.
• Fluency in Arabic language essential for effective communication.

Join our team of professionals who are passionate about delivering exceptional results. As a Medical Training Specialist, you will be responsible for creating engaging training programs that drive business growth. If you have a strong background in aesthetic dermatology products and medical devices, we encourage you to apply.

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.

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.

ID

Category

Research

Asset : Name

IROS

City

Abu Dhabi

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.

About the Role

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.

M42 is a global health champion powered by artificial intelligence (AI), technology and genomics to advance innovation in health for people and the planet. Headquartered in Abu Dhabi, M42 combines its specialized, state-of-the-art facilities with integrated health solutions like genomics and biobanks, and harnesses advanced technologies to deliver precise, preventive and predictive care, to impactfully disrupt traditional healthcare models and positively impact lives globally.

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).

Responsibilities

• 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.

Qualifications

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.

Clinical operations are at the forefront of delivering quality care and ensuring regulatory compliance in healthcare settings.

This role is pivotal in managing daily clinical trial operations for efficiency and quality, while developing operational strategies that align with organizational goals and compliance standards.

Maintaining effective communication between clinical staff, stakeholders, and regulatory bodies is crucial in this position. The successful Clinical Operations Specialist must have a strong understanding of clinical trial management, industry regulations, and attention to detail.

A Bachelor's degree in life sciences, healthcare management, or a related field is required, along with a minimum 3 years' experience in clinical operations or clinical trial management.

Excellent organizational and time-management skills, as well as analytical and problem-solving skills, are essential in addressing operational challenges and coordinating efforts across departments.

The ideal candidate will possess excellent communication and interpersonal skills, with the ability to manage multiple projects and priorities effectively.

This role involves coordinating clinical trials, project timelines, and collaborating with various stakeholders such as medical professionals, regulatory bodies, and internal teams.

A successful Clinical Operations Specialist requires a strong understanding of clinical research processes and regulatory requirements.

Key responsibilities include:

• Coordinate daily clinical trial operations for efficiency and quality.
• Develop operational strategies aligning with organizational goals and compliance standards.
• Monitor project timelines and budgets for adherence to planned schedules and cost constraints.
• Maintain effective communication between clinical staff, stakeholders, and regulatory bodies.
• Ensure clinical operations adhere to ethical guidelines and industry regulations.
• Collaborate with research teams on clinical trials and studies.
• Identify and resolve operational issues, optimizing processes for improved clinical outcomes.
• Present reports on clinical operations performance and progress to senior management.
• Train staff on clinical procedures, compliance requirements, and operational protocols.
• Assist in quality assurance and risk management plans.
• Maintain comprehensive documentation of clinical trial activities.

Job Title:

We are seeking an accomplished educator to lead our medical education curriculum development, implementation, and evaluation.

The ideal candidate will work closely with department stakeholders to deliver high-quality teaching and assessment programs that meet the needs of students and healthcare professionals.

• Curriculum Development: Design and implement outcome-based medical education curriculum that aligns with departmental goals and standards.
• Collaboration: Liaise with program directors, course coordinators, and faculty to ensure effective delivery of medical education curriculum.
• Evaluation: Contribute to the evaluation of faculty teaching and learning outcomes to inform curriculum improvement.

About the Role:

• Teach and assess students in various medical education settings.
• Lead and contribute to the development and implementation of medical education policies and procedures.
• Provide expert advice and guidance on medical education matters to senior leaders.
• Supervise and mentor junior faculty members.

Qualifications:

• PhD in Medical Education or a related field, with a Master's degree in Education (minimum requirement).
• MBBS(MD) with a PhD in Medical Education (preferred qualification).

Preferred Skills:

• Experience in Problem-Based Learning and/or Team-Based Learning.
• Leadership experience in medical education curriculum development and implementation.
• Research experience and publication record.
• Excellent organizational, interpersonal, and leadership skills.

About Us:

We offer a dynamic and supportive work environment that fosters growth and collaboration. Our team is dedicated to delivering exceptional educational experiences for students and healthcare professionals.

CATEGORY

Faculty Members College of Medicine

COLLEGE

Medicine

DEPARTMENT

Family and Community Medicine and Behavioral Sciences

JOB PURPOSE

To participate in the teaching, curriculum management and educational innovation in the college, to work closely with the Dean of College of Medicine, to supervise the PhD Program in Medical Education and Master of Leadership in Health Professions Education. Moreover, to plan and implement faculty development activities aiming at enhancing the effectiveness of the teaching and Learning, students' assessment, and educational research in the College of Medicine

MAIN ACCOUNTABILITIES & EXPECTATIONS

• Supervise the proposed PhD in Medical Education and the existing Master of Leadership in Health Professions Education.
• Provide support and advice to the Dean in matters pertaining to the curriculum delivery and assessment at under and post graduate level.
• Supervise the development of the policies and procedures for effective management of the curricula in the college of Medicine.
• Contribute to faculty development program provided by the medical education center.
  Supervise the activities of the Medical Education Centre.

REQUIRED SKILLS

• Experience in Leadership in Medical/Health Professions Education with proved track records in Medical Education field.
• Significant teaching record at both undergraduate and graduate level.
• Substantial track record of research in Medical/Health Profession Education
• Significant research activities in highly impact journals.
• Experience in supervising students in PhD Programs in Medical/Health Professions Education.
• Leadership in Medical/Health Professions Education

Qualifications:

• PhD in Medical/Clinical or Health Profession Education
• Qualification in Leadership in Medical/Health Professions Education will be an added value
• Bachelor in Medicine will be an added value

DESIRABLE REQUIREMENTS

JOB LOCATION

University of Sharjah (Main)

JOB CRITERIA

GENDER

, Male, Female,

QUALIFICATIONS

Phd

RELEVANT EXPERIENCE

9

LIVING IN UAE

Open for all

NATIONALITY

, All,