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Profile Details
USD 80 /hr
Hire Dr. Reham M.
United Arab Emirates
USD 80 /hr

Medical Communications Consultant & Writer

Profile Summary
Subject Matter Expertise
Writing Clinical Trial Documentation, Medical Writing, General Proofreading & Editing
Research Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection
Consulting Healthcare Consulting
Work Experience

Medical Communications Consultant & Writer


April 2016 - Present

Assistant Professor of Natural and Applied Sciences

University of Dubai

August 2017 - January 2020

Postdoctoral Fellow | Postgraduate researcher

United Arab Emirates University

March 2011 - April 2016

Science Advisor | Curriculum Support Specialist

Nord Anglia Education

August 2007 - March 2011

Research and Teaching Assistant

Jordan University of Science and Technology

August 2000 - August 2002


PhD in Molecular Cellular Pathology

United Arab Emirates University

March 2011 - February 2015

MSc Clinical Biochemistry

University of Newcastle-upon-Tyne, UK

September 1996 - September 1997

  • Certification details not provided.
Milhem, R.M., Ali, B.R.(2019). Disorders of FZ-CRD; Insights towards FZ-CRD folding and therapeutic landscape . Molecular Medicine. 26. (1).
Ahmad, M.A., Milhem, R.M., Panicker, N.G., Rizvi, T.A., Mustafa, F.(2016). Electrical characterization of DNA supported on nitrocellulose membranes . Scientific Reports. 6.
Milhem, R.M., Al-Gazali, L., Ali, B.R.(2015). Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome . International Journal of Biochemistry and Cell Biology. 60. p. 119-129.
Matlik, H.N., Milhem, R.M., Saadeldin, I.Y., Al-Jaibeji, H.S., Al-Gazali, L., Ali, B.R.(2014). Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian family . Pediatric Neurology. 51. (1). p. 165-169.
Milhem, R.M., Ben-Salem, S., Al-Gazali, L., Ali, B.R.(2014). Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy . Investigative Ophthalmology and Visual Science. 55. (6). p. 3423-3431.
Saadeldin, I.Y., Milhem, R.M., Al-Gazali, L., Ali, B.R.(2013). Novel KCNQ2 mutation in a large emirati family with benign familial neonatal seizures . Pediatric Neurology. 48. (1). p. 63-66.
Ali, B.R., Ben-Rebeh, I., John, A., Akawi, N.A., Milhem, R.M., Al-Shehhi, N.A., Al-Ameri, M.M., Al-Shamisi, S.A., Al-Gazali, L.(2011). Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia . PLoS ONE. 6. (10).