About Galvanize Therapeutics Galvanize is a biomedical platform company operating at the convergence of engineering, biology, and healthcare delivery, aiming to deliver life-changing solutions to patients and their doctors. Backed by Norwest.
About the role
This role pays between $145,000 and $165,000 pe r year, and your actual base pay will depend on your location, skills, qualifications, and experience. Galvanize offers a robust benefits package to full-time employees, including medical, dental, and vision coverage, life insurance, short- and long-term disability protection, 401(k), and flexible paid time off. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Experience in the medical device industry required, oncology clinical trials is preferred
- Experience in authoring and reviewing clinical documents
- Working knowledge of the GCP, ICH and FDA guidance and regulations for clinical trials
- Comfortable analyzing data and preparing audience-appropriate summaries (e.g. reports, presentations, etc.) for various stakeholders
- Proficiency with one or more standard statistical software packages (e.g. SAS, R, SPSS, MiniTab, etc.) preferred
- Highly curious, and self-motivated to use existing data to drive future clinical and medical development
More about this role
The focus of the Sr. Clinical Scientist will be to provide scientific and writing support for clinical strategy, clinical trial development, data analysis and visualization, and clinical data dissemination via presentations and publications. The Sr. Clinical Scientist will be responsible for critical reviews of internally and externally facing documents, and for interaction with internal and external stakeholders including, regulatory and commercial teams, and KOLs, physicians, and clinical staff.
Qualifications
- Bachelor’s degree in Life Sciences, engineering, statistics, or related field required. Advanced degree (MS, PhD, MD) preferred.
- A minimum of 12 years’ experience in clinical research focused on managing clinical science/research activities.
- Experience in the medical device industry required; oncology clinical trials is preferred.
- Experience in authoring and reviewing clinical documents
- Working knowledge of the GCP, ICH and FDA guidance and regulations for clinical trials
- Comfortable analyzing data and preparing audience-appropriate summaries (e.g. reports, presentations, etc.) for various stakeholders.
- Proficiency with one or more standard statistical...
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