Senior Medical Writer - job 1 of 2

As a Senior Medical Writer at Eikon Therapeutics, you'll be responsible for authoring and editing a range of critical documents including clinical protocols, study reports, and investigator brochures. You'll collaborate with various cross-functional teams to ensure that documents are high-quality, accurate, and fit for use in clinical studies. Additionally, you'll manage the document lifecycle, which encompasses timelines, writing assignments, and quality management.

To be considered for the Senior Medical Writer role at Eikon Therapeutics, candidates typically need a doctoral-level degree in Life Sciences, or a Master’s degree with relevant experience. A Bachelor’s degree with extensive experience in medical writing is also acceptable. Experience in writing clinical study protocols and knowledge of regulatory guidelines is desirable for this position.

At Eikon Therapeutics, the work environment for the Senior Medical Writer is collaborative, fast-paced, and dynamic. The role requires onsite presence at least three days a week in our Jersey City office or other locations, fostering collaboration with team members to ensure effective project management and high-quality deliverables for our clinical studies.

Successful Senior Medical Writers at Eikon Therapeutics should possess excellent communication, presentation, and project management skills. It's also important to have strong attention to detail, the ability to interpret scientific data, and familiarity with regulatory documents. Technical skills in document preparation software and a deep understanding of clinical development processes are critical for success in this role.

Eikon Therapeutics values the growth of its employees. Senior Medical Writers can find numerous opportunities for professional development, including the chance to take on additional responsibilities, lead projects, and participate in team collaborations that may pave the way for career advancement within the organization as Eikon continues to expand.

In answering this question, focus on specific examples of clinical research documents you have authored or edited, such as clinical protocols or study reports. Highlight key challenges you faced and how you overcame them to ensure regulatory compliance and quality of the documents.

To answer this, talk about the processes you follow, such as using style guides, implementing quality control checks, and soliciting feedback from peer reviews. Mention any tools or software you utilize that help maintain accuracy across documents.

Detail your time management and prioritization strategies. Mention tools you use for organizing deadlines and assignments and how you communicate effectively with team members to keep projects on track.

Choose a specific example where you interpreted scientific data. Discuss your approach to translating complex data into clear and concise formats, ensuring it aligns with regulatory requirements and maintains clarity for the intended audience.

Emphasize the importance of team interactions, how you work with cross-functional teams to gather input and insights, and how collaboration enhances the quality of medical writing. Provide examples where collaboration led to improved outcomes.

Discuss specific types of regulatory documents you have worked on, such as investigator brochures or clinical study reports. Explain your familiarity with guidelines and how you ensure compliance in your writing.

Talk about the resources you use, such as professional organizations, conferences, webinars, and journals that keep you informed about the ever-evolving field of medical writing and regulatory requirements.

Share your thoughts on essential qualities like attention to detail, adaptability, excellent communication skills, and strong analytical abilities. Provide examples of how these qualities have positively impacted your work.

Discuss trends you've observed in the industry, such as the growing importance of compliance, the role of technology in document management, or shifting regulatory landscapes. Highlight your readiness to adapt to upcoming changes.

Be sure to express your passion for Eikon's mission in developing innovative therapies. Discuss how your skills align with their objectives and how you see yourself contributing to their growth and success.