Clinical Communications Specialist

Clinical Communications Specialist
  • posted job: 2025-07-08
  • Dubai
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  • Job Country: UAE
  • Job Industry: Biotechnology & Life Sciences
  • Job Profile: Medical Affairs Specialist
  • Training Duration: Not Required
  • Number of Jobs Opening: 50
  • Salary: 190000 ( 190000 Per Month)
  • Job Type: Full Time
  • Visa: Provided by company
  • Food: Provided by company
  • Accommodation: Provided by company
  • Air ticket: Provided by company
  • Medical Insurance: Provided by Company
  • Commuting to job location: Provided by company
  • Required Experience: 4 Years
  • Minimum Education Level: Bachelor’s Degree
  • Employee Acceptance: International
  • Work Location: Work at Office/Being at Work
  • Hiring Need: Immediate

Job Description:

The Clinical Communications Specialist plays a key role in developing, reviewing, and disseminating scientific and clinical content tailored to healthcare professionals, regulatory bodies, and internal stakeholders. This role ensures that complex clinical information is accurately translated into clear, concise, and compliant communication materials. Responsibilities include preparing medical newsletters, clinical slide decks, educational materials, manuscripts, abstracts, and regulatory submissions. The specialist will collaborate with medical writers, regulatory teams, clinical researchers, and brand managers to align messages with therapeutic strategies and scientific standards. They may also support internal training, external presentations, and conference materials. This role requires the ability to interpret clinical data, conduct literature reviews, and adapt tone and format to suit various audiences. It is essential to ensure scientific accuracy, regulatory compliance, and brand consistency in all outputs. The specialist must maintain up-to-date knowledge of therapeutic areas, competitive landscape, and regulatory guidelines, contributing to effective knowledge dissemination and medical education initiatives.

Job Requirement:

A bachelor’s or master’s degree in biomedical sciences, pharmacy, or medical communications is required, with 3–5 years of experience in scientific writing, medical affairs, or regulatory communications. Strong command of English language, attention to detail, and the ability to work under pressure are essential. Proficiency with referencing tools (EndNote), literature databases (PubMed), and formatting guidelines (e.g., ICMJE, AMA) is expected. Candidates should possess excellent organizational skills and be comfortable working across multiple projects simultaneously.

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