[Voronoi, Inc.] Medical Writer (Hybrid Work)

VORONOI, Inc.; Cambridge (MA); Hybrid; USD 110,000 - 170,000; Full time

Job summary

Voronoi, Inc. is seeking an experienced Medical Writer with a strong background in oncology clinical trials.

This hybrid role requires minimum 2 days onsite in Waltham, MA / Cambridge area, supporting regulatory and scientific documents for oncology programs. The candidate will write, edit, and manage sections of regulatory submissions, while mentoring junior writers and aligning with ICH-GCP guidelines and SOPs.

Qualifications

• Advanced degree in life sciences or related field.
• 5+ years medical writing experience, with 3+ years in oncology.
• Experience with Phase I–III oncology trials & regulatory submissions.
• Strong knowledge of ICH-GCP and FDA/EMA guidelines.
• Excellent written and verbal communication; attention to detail.

Responsibilities

• Develop, write, and edit clinical and regulatory documents for oncology trials.
• Prepare protocols, CSRs, IBs, informed consent forms, and briefing documents.
• Contribute to regulatory submissions (INDs, NDAs, BLAs) and timelines.
• Collaborate with cross-functional teams to ensure accuracy and consistency.
• Mentor junior medical writers and stay current with guidance and trends.

Skills

Medical writing

Oncology knowledge

Regulatory writing

ICH-GCP knowledge

Project management

Editorial rigor

Education

PhD/MD/PharmD/MSc in life sciences or related

Tools

MS Office Suite

Document management systems

Job description

[Voronoi, Inc.] Medical Writer (Hybrid Work)

Medical Writer - Oncology Clinical Trials

Location: minimum 2 days onsite in Waltham, MA office Cambridge / Greater Boston

Position Summary:

We are seeking an experienced Medical Writer with a strong background in oncology clinical trials to join our growing company. The ideal candidate will have a deep understanding of oncology therapeutic areas and a proven track record of preparing high-quality regulatory and scientific documents in support of clinical development programs.

Key Responsibilities:

• Develop, write, and edit clinical and regulatory documents related to oncology clinical trials, including but not limited to:
• Clinical study protocols and amendments
• Investigator brochures
• Clinical study reports (CSRs)
• Informed consent forms
• Briefing documents
• Clinical sections of INDs, NDAs, BLAs, and other regulatory submissions
• Collaborate with cross-functional teams including Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and Safety teams to ensure content accuracy and consistency
• Interpret and synthesize complex clinical and scientific data into clear, concise, and scientifically sound documents
• Ensure all documents comply with ICH guidelines, regulatory requirements, and internal SOPs
• Participate in strategic planning and document timelines
• Mentor junior medical writers or contractors as needed
• Stay current with therapeutic area developments, industry trends, and regulatory guidance

Qualifications:

• Advanced degree (PhD, PharmD, MD, or MSc) in life sciences, medicine, or a related field
• Minimum 5 years of medical writing experience, with at least 3 years focused on oncology clinical trials
• In-depth understanding of oncology disease areas and clinical endpoints
• Extensive experience in authoring documents for Phase I–III oncology trials and regulatory submissions
• Strong knowledge of ICH-GCP, FDA/EMA guidelines, and clinical trial processes
• Excellent written and verbal communication skills
• High attention to detail, strong analytical skills, and ability to manage multiple projects under tight deadlines
• Proficiency with document management systems and MS Office Suite; experience with templates and style guides

Preferred Qualifications:

• Experience working in a CRO, biotech, or pharmaceutical company
• Familiarity with submission processes (eCTD) and regulatory publishing
• Membership in professional organizations such as AMWA or EMWA is preferred