Medical Writer

Position Overview

The SerenaGroups is looking for a highly skilled and detail-oriented Medical Writer to join our growing team. In this role, you’ll put your scientific expertise and writing talent to work, translating complex medical and scientific information into content that’s clear, accurate, and genuinely engaging. You’ll craft materials for a wide range of audiences—from healthcare professionals and regulatory authorities to patients and the general public.

Your projects might range from technical, scientific documents (regulatory submissions, clinical research reports, journal articles) to marketing and educational content (press releases, patient brochures, training modules). If you’re passionate about clear communication and want your work to make a difference, you’ll fit right in.

Key Responsibilities

• Work closely with subject matter experts, researchers, and technical teams to gather and organize information on new products, treatments, and procedures.
• Research and review medical topics; help physicians draft research articles and review papers.
• Prepare and edit press releases, training materials, and marketing communications.
• Write concise articles, reports, and summaries on medical and scientific discoveries.
• Communicate complex medical concepts in accessible, audience-appropriate language.
• Collaborate with clinical research teams on study protocols and trial documents.
• Draft, edit, and review clinical research materials (study reports, investigator brochures, regulatory submissions).
• Prepare annual reports, abstracts, brochures, and presentation materials.
• Develop training manuals and eLearning content tailored to various audiences.
• Ensure all work complies with relevant guidelines, regulations, and industry standards.
• Stay current on evolving medical terminology, research trends, and regulatory requirements.

Why Join Us?

At SerenaGroups, our values drive everything we do: integrity, putting patients first, service, respect, collaboration, and a proper family environment. We’re passionate about making a difference for our partners and patients and always strive to grow and innovate.

Here’s what you’ll find here:

• The chance to work on diverse and meaningful healthcare and life sciences projects.
• Collaboration with leading experts and forward-thinking innovators in the field.
• Competitive pay, benefits, and real opportunities for professional growth.

If you’re ready for your work to have a real impact—and want to be part of a values-driven team—we’d love to hear from you.

To Apply:
Send your resume, a brief cover letter, and relevant writing samples to [your email address].

SerenaGroups is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Education & Experience Requirements

• Bachelor’s degree in English, Journalism, Life Sciences, or a related field (Master’s or Ph.D. preferred; equivalent experience considered).
• Solid grounding in life sciences, medicine, pharmacy, or a related discipline is highly desirable.
• Previous experience in medical writing—scientific, technical, or marketing—is required.
• Certification from a recognized medical writing association is a plus, but not required.

Core Competencies & Personal Attributes

• Outstanding written and verbal communication skills.
• Meticulous attention to detail and scientific accuracy.
• Mastery of grammar, language usage, and style guidelines.
• Ability to interpret and communicate statistical results.
• Strong research and analytical skills.
• Critical thinking and problem-solving ability.
• Self-motivated, curious, and committed to continuous learning.
• Capable of managing multiple projects and meeting deadlines.
• Collaborative mindset, comfortable working independently or as part of a multidisciplinary team.

Technical Skills

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and online research databases (e.g., PubMed, Medline).
• Familiarity with AMA, APA, or other scientific style guides.
• Understanding of clinical research processes, regulatory guidelines (FDA, EMA, ICH), pharmacology concepts, and drug safety requirements.