Verve Therapeutics is a biotechnology company created with a singular focus to protect the world from heart disease. Verve is committed to discovering and developing therapies that safely edit the genome of adults to confer lifelong protection from coronary artery disease, the most common form of heart disease and the leading cause of death worldwide. Headquartered in Cambridge, Massachusetts, Verve was founded by world-leading experts in cardiovascular medicine and gene editing and is backed by a top-tier syndicate of investors, including GV (formerly Google Ventures), ARCH Venture Partners, F-Prime Capital Partners, and Biomatics Capital.
Verve is seeking a Preclinical Study Coordinator to support multiple preclinical programs and be responsible for establishing and maintaining effective sourcing of in vitro and in vivo pharmacology studies. The individual will act as the liaison between Verve and its Contract Research Organizations (CROs) to confirm and track deliverables of collected samples, data and reports to ensure alignment of supporting studies is properly coordinated. Responsibilities may include some or all the following:
• Collaborate closely with internal study teams and CROs to coordinate and track study deliverables
• Assist in scheduling creation, distribution and review of study-related documents
• Support study project time-lines and protocol execution
• Provide project management support with current studies
• Support implementation and management of study data through file management and document control
• Assist in the planning and preparation for study-related meetings with internal study teams and CROs
• Assist with study reports and presentations
This role requires excellent communication skills and the ability to rapidly identify and escalate issues and opportunities as appropriate. Candidates should have earned a degree in biology, biochemistry, pharmacy or related area and should Have a BS/MS or equivalent degree with a focus in in biology, biochemistry, toxicology or a related field and at least 3 years of experience in a biopharmaceutical company. Experience as a study monitor and/or project management tools in a preclinical setting is essential.
Verve Therapeutics is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability or special need that requires accommodation, please let us know.
Recruitment & staffing agencies
Verve Therapeutics does not accept agency resumes unless contacted directly by internal Verve Talent Acquisition. Please do not forward resumes to our email@example.com account, Verve employees or any other company location; Verve Therapeutics is not responsible for any fees related to unsolicited resumes.