About Job

Job Title: Training Content Writer (Entry Level)

Summary:

This entry-level position requires excellent writing and communication skills, plus a commitment to creating informative, accurate, and engaging training materials. The primary focus is on developing content related to standard operating procedures for clinical trials, with opportunities to support other training initiatives as well.

Essential Functions:

Develop and Produce Training Content: Design, develop, and write comprehensive training materials for diverse audiences, including clinical research professionals, site staff, and patients involved in clinical trials.
Content Formats: Create a range of materials such as protocols, case report forms, informed consent forms, study reports, manuscripts, regulatory submissions, educational videos, web-based modules, and presentation slides.
Research and Subject Matter Expertise: Conduct in-depth research on wound care topics, clinical trial methodology, and relevant regulatory guidelines (e.g., FDA, EMA, ICH). Work closely with clinicians, researchers, and regulatory specialists to gather and verify information.
Regulatory Compliance: Ensure all training materials comply with regulatory requirements, industry standards, and Good Clinical Practice (GCP) guidelines.
Simplify Complex Information: Translate complex medical and scientific content into clear, concise, and audience-appropriate language.
Leverage AI Technologies: Use AI tools to maintain accuracy, consistency, and standardization across all training materials.
Edit and Proofread: Review and refine content for grammar, clarity, style, and technical precision.
Project Management: Handle multiple projects simultaneously and meet strict deadlines.
SOP and Medical Writing: Develop or revise standard operating procedures and contribute to clinical trial-related medical writing.
Continuous Learning: Stay up-to-date with new medical discoveries, regulatory changes, and industry best practices.
Contribute to Training Programs: Support the design and implementation of training programs, workshops, and educational initiatives.

Qualifications:

Technical Proficiency: Experience with AI platforms/technologies, presentation software, and content management systems.
Education: Bachelor’s degree in a relevant field (medical sciences, journalism, communications) or equivalent experience.
Experience: 1-2 years’ experience (internships, freelance, or full-time) in medical or scientific writing, with an emphasis on clinical trials.
Writing Skills: Exceptional written and verbal communication skills, with the ability to produce clear, concise, and engaging content.
Medical Knowledge: Willingness and ability to learn medical terminology, concepts, and principles, especially in wound care and clinical research.
Regulatory Knowledge: Ability to learn and apply regulatory guidelines and best practices for clinical trials and medical devices.
Research Skills: Demonstrated research and analytical ability for gathering and evaluating scientific information.
Attention to Detail: High degree of accuracy and meticulousness.
Collaboration: Strong teamwork skills and the ability to work effectively with subject matter experts.