Clinical Scientist

Voronoi; Waltham (MA); Hybrid; USD 190,000 - 270,000; Full time

Benefits offered by this job

Hybrid work environment

Travel up to 15%

Job summary

Voronoi, an oncology-focused biopharmaceutical company, seeks a senior-to-director level clinical development expert to lead the design, execution, and reporting of early-phase oncology trials. You will author core documents, review clinical data, and collaborate with Regulatory, Translational Science, and Clinical Operations to ensure data integrity and regulatory readiness.

You will mentor junior staff, drive scientific communication, and contribute to cross-functional study teams in a

Qualifications

• 10+ years of clinical development experience in oncology.
• Experience with protocol development, data review, CSR preparation, and cross-functional study teams.
• Familiarity with GCP, ICH, FDA/EMA regulatory guidelines.
• Strong communication skills and ability to work in a global, fast-paced environment.

Responsibilities

• Design, execution, and reporting of early-phase oncology trials.
• Lead authoring/review of study protocols, investigators brochures, CSRs, and informed consent forms.
• Medical data review, safety surveillance, and interim/final analyses preparation.
• Ensure consistent scientific messaging across documents, publications, and presentations.
• Mentor junior team members and contribute to process improvements within Clinical Science.

Skills

Oncology clinical development

Data interpretation

Regulatory submissions

Scientific communication

Mentoring

Education

PhD/PharmD/MD

Master’s with oncology development experience

Job description

Location: minimum 2 days on site in Waltham, MA office

Reports to: Head of Clinical Development

Employment Type: Full-time

Experience Level: 10+ years (PhD, PharmD, or MD preferred) / Senior to Director

[Company Description]

Founded in 2015, Voronoi, Inc. (KOSDAQ:310210) is a clinical-stage biopharmaceutical company developing innovative, precision-targeted therapies in oncology. Operating across the U.S. and South Korea, we combine translational research, structure-based drug design, and data-informed development to advance next-generation treatments that address critical unmet needs for patients with oncologic diseases.

[Position Overview]

This position will serve as a key scientific member of the Clinical Development team, providing scientific and operational contributions across one or more clinical studies.

The individual in this role will ensure the design, execution, and reporting of high-quality clinical trials through effective data review, document authorship, and cross-functional collaboration.

Success in this role requires substantial oncology experience, strong teamwork across clinical and scientific functions, and the ability to synthesize complex data into clear, actionable outputs that inform clinical decision‑making.

[Key Responsibilities]

Study Execution and Scientific Oversight

• Contribute to the design, implementation, and reporting of early phase oncology trials.
• Lead authoring and review of clinical documents including study protocols, investigator brochures, clinical study reports (CSRs), and informed consent forms.
• Participate in medical data review, safety surveillance, and preparation of interim and final study analyses.
• Ensure consistency of scientific messaging across study documents, publications, and presentations.

Cross‑Functional Collaboration

• Partner with Clinical Operations, Biostatistics, Regulatory Affairs, and Translational Science to ensure data quality and scientific integrity.
• Support preparation of regulatory submissions and responses
• Contribute to KOL engagement and investigator interactions as part of clinical team representation.

Data Interpretation and Communication

• Summarize and interpret emerging efficacy and safety data for internal meetings and external dissemination.
• Support preparation of abstracts, posters, and manuscripts for scientific conferences.

Functional Excellence

• Mentor junior team members and contribute to the continuous improvement of Clinical Science processes.

[Qualifications]

• PhD, PharmD, or MD in a life‑science discipline strongly preferred; Master’s degree with significant oncology development experience will be considered.
• Approximately 10 years years of clinical development experience in oncology within a biopharma or biotech setting.
• Hands‑on experience with protocol development, data review, CSR preparation, and cross‑functional study team participation.
• Familiarity with GCP, ICH, and global regulatory guidelines (FDA/EMA).
• Strong communication skills with ability to convey complex scientific concepts clearly.
• Proven ability to work effectively in a global, matrixed, fast‑paced environment.

[Additional Information]

• Hybrid work environment (minimum 2 days onsite in Cambridge / Greater Boston).
• Flexible hours to accommodate collaboration across global teams.
• Occasional travel (≤15%) for investigator meetings, conferences, and cross‑site activities.

Join a dynamic oncology biotech where your scientific expertise directly contributes to advancing first‑in‑class therapies for patients with oncologic diseases worldwide.

At Voronoi, we value collaboration, integrity, and curiosity — and we empower every team member to make a meaningful impact.

Voronoi is proud to be an equal opportunity employer. We are committed to fostering a diverse and inclusive workplace where every individual is valued, respected, and empowered to contribute to our shared mission of advancing transformative oncology therapies. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other characteristic protected by applicable law.