Senior Manager
Etmf Management
Posted on 1/31/2024
Tango Therapeutics

51-200 employees

Develops targeted cancer therapies using synthetic lethality
Company Overview
Tango Therapeutics, a biotechnology firm, stands out due to its unique approach to cancer treatment, utilizing advances in DNA sequencing and CRISPR-based target discovery to develop novel medicines targeting cancer vulnerabilities. The company's focus on synthetic lethality, a method that targets specific genes in cancer cells leaving normal cells largely unaffected, offers a potential for enhanced anti-tumor efficacy and reduced toxicity. Furthermore, Tango's patient-centric approach and deep understanding of genetic subtypes of cancer enable it to identify novel drug targets and combinations, accelerating the development of transformational new therapies for patients with well-defined populations currently lacking effective treatment options.
Data & Analytics
Biotechnology

Company Stage

N/A

Total Funding

$537M

Founded

2017

Headquarters

Boston, Massachusetts

Growth & Insights
Headcount

6 month growth

9%

1 year growth

16%

2 year growth

47%
Locations
Cambridge, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
Management
Google Cloud Platform
PowerPoint/Keynote/Slides
CategoriesNew
Product
Requirements
  • Life sciences degree or certification in a related allied health field
  • 3-5 years’ experience with clinical trials (e.g., study coordinator, regulatory operations) and electronic TMF document management experience
  • Clear and timely communication skills
  • Understanding of GCP and regulatory requirements as well as a working knowledge of clinical research documents, their contents and purpose
  • Demonstrated proficiency with MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint
Responsibilities
  • Maintain effective communication with project teams, CRO staff, and vendors throughout study start-up, maintenance, and close-out
  • Support study document filing into the trial TMF
  • Review and ensure compliance and oversight of TMF plans
  • Perform routine quality checks of documents uploaded into the TMF across trials, and ensure findings are documented and resolved in a timely manner
  • Respond to inquiries regarding TMF management and contents
  • Attend departmental and study-specific meetings and discussions, as required
  • Run routine TMF reports and monitor for completeness and trends
  • May provide TMF training to new team members
  • Perform general administrative tasks
  • Complete other study document-related tasks as required by the study teams
  • Additional duties and responsibilities as required