Medical Writer
Full time, hybrid (in the office 2 days per week)
We are looking for a talented and detail-oriented Medical Writer to join our dynamic team. This role offers an exciting opportunity for an individual with a strong background in medical writing to contribute to the creation of high-quality content that communicates complex scientific information to various audiences.
Position summary: You will play a crucial role in translating scientific and clinical data into clear and compelling written content for a variety of purposes, including regulatory documents, clinical trial protocols, scientific publications, promotional materials and educational resources. You will work closely with cross-functional teams to ensure accurate and effective communication of medical and scientific information.
Key responsibilities
- Content development
- Create, edit, and review scientific and medical content for regulatory submissions, clinical trial documentation, and other written materials
- Develop clear and concise summaries of complex clinical trial results, data analyses, and scientific literature
- Regulatory compliance
- Ensure that all written materials comply with relevant regulatory guidelines and industry standards
- Collaborate with regulatory affairs professionals to support the preparation of regulatory submissions
- Cross-functional collaboration
- Work closely with cross-functional teams to understand project requirements and contribute to the development of strategic communication plans
- Collaborate with subject matter experts to gather information and ensure accuracy in content
- Literature review
- Conduct literature reviews to stay informed about the latest developments in the field and incorporate relevant information into written materials
- Quality assurance
- Implement quality control processes to ensure accuracy, consistency and adherence to company standards in all written deliverables
- Qualifications
- Advanced degree in a relevant scientific or medical field (e.g., Masters, PhD, MD, PharmD)
Core capabilities
- Proven experience in medical writing
- Strong understanding of regulatory guidelines (e.g., ICH, FDA)
- Excellent written and verbal communication skills
- Ability to work collaboratively in a fast-paced, team-oriented environment
- Proficiency in using relevant software tools for document preparation and management
How to apply
Interested candidates should submit their resume, a cover letter, and writing samples demonstrating their medical writing expertise. If you choose to contact us via email, please include ‘Medical Writer Application’ in the subject line.
Frontera Group is an equal opportunity employer and encourages candidates from diverse backgrounds to apply. We thank all applicants for their interest; however, only those selected for an interview will be contacted.