Medical Writer Job at M42 Health | Apply Now
Medical writer job opportunities are growing rapidly in the healthcare and clinical research industry, and M42 Health is offering an exciting role in Abu Dhabi, United Arab Emirates. This clinical research job is ideal for experienced professionals with expertise in medical writing, real-world evidence studies, and clinical trial documentation. Candidates looking for jobs in Abu Dhabi within a leading AI-powered healthcare organization can explore this excellent opportunity with IROS under M42 Health.
- Job Position: Medical Writer
- Location: Abu Dhabi, United Arab Emirates
- Department: Clinical Research
- Organization: IROS (Insights Research Organization & Solutions)
- Job Code: 5417
About the Company
Medical writer job opportunities at M42 Health provide professionals with the chance to work in an innovative healthcare environment powered by artificial intelligence, genomics, and advanced technology. M42 is a global healthcare organization headquartered in Abu Dhabi and focuses on delivering precise, preventive, and predictive healthcare solutions.
Under M42, Insights Research Organization & Solutions (IROS) operates as the UAE’s first homegrown Contract Research Organization (CRO). IROS is dedicated to advancing healthcare research through world-class clinical trials, regulatory expertise, and data-driven healthcare solutions that support global healthcare innovation.
Medical Writer Job Description
Medical writer job responsibilities at IROS involve supporting both clinical trial and real-world evidence (RWE) studies. The Medical Writer will independently lead the development of high-quality medical writing deliverables across multiple projects while ensuring compliance with regulatory standards and agreed timelines. The role supports business growth by increasing writing capacity and ensuring study documentation is delivered with scientific accuracy, clarity, and consistency. The Medical Writer will collaborate closely with cross-functional teams, medical writers, sponsors, and investigators throughout the document lifecycle, from study design to finalization.
Qualifications Required
Medical writer job applicants should possess strong scientific writing expertise and experience within pharmaceutical companies or CRO environments.
Educational Qualifications
- Bachelor’s or Master’s degree in Life Sciences or a related discipline such as:
- Biology
- Biochemistry
- Physiology
- Genetics
Experience Required
- Minimum 4 years of experience as a Medical Writer in a pharmaceutical company or CRO.
- Experience independently authoring:
- Clinical trial protocols
- Informed consent forms (ICFs)
- Study reports
- Experience in real-world evidence (RWE) and observational research writing.
Skills and Knowledge
- Strong understanding of ICH-GCP and regulatory guidelines including FDA and EMA.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects within tight deadlines.
- Strong organizational and time-management skills.
- Ability to work independently and collaboratively.
- GCP certification preferred.
Key Responsibilities – Medical Writer Job
Medical writer job duties include managing clinical research documentation and collaborating with multiple healthcare teams to ensure high-quality deliverables. Responsibilities Include:
- Independently develop clinical trial and real-world evidence documents.
- Design and develop retrospective and prospective clinical study protocols and amendments.
- Prepare study concepts, synopses, and feasibility documents.
- Develop and review informed consent forms (ICFs).
- Author and contribute to clinical study reports (CSRs).
- Review tables, figures, listings (TFL) shells, and narrative content with biometrics and biostatistics teams.
- Collaborate with clinical operations, biometrics, biostatistics, and regulatory teams.
- Manage multiple projects and documentation timelines simultaneously.
- Participate in internal and external review cycles and resolve comments accurately.
- Engage with sponsors, investigators, and internal stakeholders during document development.
- Ensure compliance with ICH-GCP guidelines, FDA, EMA, and internal SOPs.
- Maintain document version control and quality review standards.
Why Apply for This Clinical Research Job?
Medical writer job seekers searching for jobs in Abu Dhabi can benefit from working with a globally recognized healthcare innovator. M42 Health offers exposure to advanced healthcare technologies, genomics, and impactful clinical research projects while supporting professional growth in the healthcare and pharmaceutical industry.
This opportunity is ideal for professionals looking to expand their expertise in clinical trial documentation, real-world evidence studies, and regulatory medical writing within a leading CRO environment.
