7 Clinical Trials jobs in the United Arab Emirates

Unlocking Medical Research Innovations

A forward-thinking company is seeking an exceptional Lead Data Science Researcher to spearhead high-impact research initiatives and drive innovation in applied machine learning.

This opportunity offers a chance to explore uncharted territory with a strong technical team and push the boundaries of medical and clinical data analysis.

The ideal candidate will lead a compact team of data scientists, guiding them on experimental projects and high-impact research initiatives that transform complex problems into innovative solutions using machine learning techniques.

Key Responsibilities:

• Driving innovation in applied machine learning, particularly in medical and clinical data.
• Leading a team of data scientists on high-impact research initiatives and guiding them on experimental projects.
• Developing innovative solutions to complex problems using machine learning techniques.

Requirements:

• Exceptional analytical and statistical skills, with a strong background in machine learning techniques.
• Proficiency in deep learning frameworks like PyTorch or TensorFlow.
• Excellent Python skills, with the ability to build clean, testable, production-ready code.
• Familiarity with medical or life science data is a significant advantage.
• Expertise in SQL, Pandas, Scikit-learn, and modern data workflows.
• Comfortable working in Google Cloud Platform (GCP) environments.

Preferred Experience:

• State-of-the-art NLP models, Transformers, and mixed data analysis and summarization.
• Experience with pipeline orchestration tools like Airflow, Argo, etc.
• Proven expertise in Anomaly Detection and Forecasting with explainability for temporal and mixed data.
• Intermediate+ English language proficiency, with the ability to participate in written discussions with international teams and clients.

We are seeking a highly skilled and experienced Advanced Radiologic Technologist to join our team as an Instructor. The ideal candidate will have a strong background in medical imaging research and a passion for teaching.

• Responsibilities:

1. Teaching & Training:
• Develop and deliver courses in advanced medical imaging research methodologies.
• Train students in MRI techniques and AI diagnostics.
• Supervise students in imaging research projects.
2. Research & Technical Support:
• Operate and optimize MRI protocols.
• Assist in AI-driven imaging research.
• Ensure compliance with international imaging standards.
3. Industry & Clinical Research Collaboration:
• Support clinical trials in various fields.
• Collaborate with healthcare institutions to advance research.

Requirements:

• Bachelor's degree in Radiologic Sciences or a related field.
• Professional MRI certification.

Preferred Qualifications:

• Additional certifications and experience in MRI imaging.
• Knowledge of patient safety protocols.
• Active HAD license.

Expected Skills:

• Proficiency in MRI research protocols.
• Experience in clinical research and industry collaborations.
• Graduate or professional teaching experience.

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.

Join a team of innovative researchers in formulation development and play a key role in creating cutting-edge pharmaceutical products for regulated markets.

This exciting position involves hands-on research and development activities, cross-functional collaboration, and end-to-end project management from literature review to technology transfer. The successful candidate will work closely with various departments to ensure project timelines are met and deliver high-quality results.

• Conduct comprehensive literature surveys and patent searches to identify best practices and emerging trends.
• Develop Quality Target Product Profiles (QTPP) based on literature and reference product characterization, ensuring compliance with regulatory requirements.
• Finalize API and excipient sources for new product development, considering cost-effectiveness and supply chain reliability.
• Execute pre-formulation studies and drug-excipient compatibility assessments to optimize product performance.
• Drive process optimization and reformulation activities, documenting all changes and closures thoroughly.
• Prepare regulatory dossiers and support CTD documentation for submissions, working closely with regulatory affairs teams.
• Design and execute pharmaceutical experiments using Quality by Design (QbD) principles, ensuring data integrity and accuracy.
• Review analytical development data and compile comprehensive product development reports, highlighting key findings and recommendations.
• Support batch manufacturing for process optimization, regulatory submissions, and bioequivalence (BE) studies, collaborating with production teams.
• Assist with pilot and scale-up batches, including documentation and technology transfer to production, ensuring seamless execution.
• Develop and maintain R&D Standard Operating Procedures (SOPs) aligned with current Good Manufacturing Practice (cGMP) and Good Distribution Practice (GDP) standards.
• Submit periodic project reports to management for review and alignment, providing progress updates and key metrics.
• Collaborate with various departments, including Analytical R&D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs, to ensure project success.

• A Master's degree in Pharmacy or a related field is preferred, but a Bachelor's degree in Pharmacy with relevant experience may also be considered.
• A minimum of 8 years of hands-on experience in Formulation Development for regulated markets, with a proven track record of addressing regulatory queries and inquiries.
• Strong background in developing and handling multiple dosage forms, particularly Biosimilars and Injectables, with expertise in Technology Transfer and Contract Manufacturing processes.

We value diversity and inclusion, and welcome applications from talented individuals who share our commitment to excellence and innovation. Apply today and join our dynamic team of researchers and scientists!