3 Clinical Safety jobs in the United Arab Emirates

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

We are seeking an experienced Drug Safety Coding Specialist with a strong background in pharmacovigilance terminology and regulatory coding standards.

• Perform accurate and consistent coding of adverse events, medical history, lab terms, and concomitant medications using MedDRA and WHO-DD.
• Review and validate terms in Individual Case Safety Reports (ICSRs) to ensure alignment with global PV standards.
• Perform recoding or dictionary version updates in compliance with regulatory requirements.
• Collaborate with case processors, medical reviewers, and data management teams to resolve coding discrepancies.
• Ensure compliance with ICH-GCP, GVP, and internal SOPs.
• Maintain and update code lists and contribute to coding conventions development.
• Support training of new team members on dictionary use and coding best practices.
• Participate in audits, inspections, and quality control checks related to coding.

• B.Pharm / M.Pharm / PharmD / MBBS / BDS / B.Sc. Life Sciences
• MedDRA coding training or pharmacovigilance certification is a plus
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team

Interested to apply can share CV or call/WhatsApp to