Senior Clinical Scientist
Confirmed live in the last 24 hours
Verve Therapeutics

201-500 employees

Develops gene editing therapies for heart disease
Company Overview
Verve Therapeutics, a clinical-stage biotechnology company, is a leading player in the fight against heart disease, leveraging its expertise in cardiovascular medicine, human genetics, and gene editing to develop transformative, once-and-done therapies. The company's unique approach to gene editing, designed to permanently lower LDL cholesterol and triglyceride levels, sets it apart from competitors and positions it at the forefront of precision genetic medicine. With a culture that fosters passion and drive, Verve has been recognized as a "Best Places to Work" by the Boston Globe, demonstrating its commitment to both its mission and its employees.
Biotechnology

Company Stage

N/A

Total Funding

$419.3M

Founded

2018

Headquarters

Boston, Massachusetts

Growth & Insights
Headcount

6 month growth

3%

1 year growth

15%

2 year growth

94%
Locations
Cambridge, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
CategoriesNew
Medical, Clinical & Veterinary
Diagnostics & Laboratory Professionals
Requirements
  • Healthcare degree such as RN, NP, PA, BSN, MSN, Pharm D
  • 7+ years of clinical healthcare experience with a BS level degree
  • 5+ years of clinical healthcare experience with an advanced degree
  • Experience ideally in internal medicine or cardiology
  • Experience with clinical research studies or clinical development experience in industry is preferred
  • Familiarity with key clinical study documents
  • Experience with the review of clinical data
  • Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies
  • Strong attention to detail and organizational skills
  • Exceptional verbal and written communication skills
  • Ability to build strong relationships and work effectively with cross-functional teams
Responsibilities
  • Partners with other clinical scientists and medical monitor on oversight of clinical trial activities, including safety reviews and site interactions
  • Organize and lead process for review of potential patients for study participation
  • Review, analyze, and interpret emerging clinical trial data
  • Liase with the broader clinical development team at Verve (clinical operations, data management, and regulatory teams)
  • Contribute to authoring key study and regulatory documents (e.g. protocol, ICF, study manuals)
  • Leads internal meetings to review topics and develop mitigation plans
  • Contribute to the development of presentations emerging from clinical studies
  • Ensure compliance of all activities with ICH/GCP guidelines, applicable regulatory requirements, and Verve SOPs
  • Other duties as assigned