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Director – Clinical Operations
Confirmed live in the last 24 hours
Locations
Dorchester, Boston, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Google Cloud Platform
PowerPoint/Keynote/Slides
Communications
Requirements
  • Bachelor's Degree in a life science or allied health field (e.g. Nursing, Medical or Laboratory Technology) is required
  • Minimum of 5 years of experience in clinical trial operations is required
  • Minimum of 2 years of oncology experience is required
  • Early phase experience, including IND submissions, is required
  • Strong vendor management and project management skills are critical
  • Excellent written and oral communication skills
  • Strong working knowledge of GCP/ICH and other applicable regulations/guidelines is required
  • Good organizational/prioritization skills with strong attention to detail and an eye for quality
  • Strong proficiency with MS Office programs such as Outlook, Word, Excel, PowerPoint, and SharePoint is required
  • A collaborative spirit for working successfully with cross-functional teams and partners is essential
  • When safe to do so, travel will be required
Responsibilities
  • Manage clinical trials from start-up through close-out to ensure that both internal and external deliverables are on time and on budget as well as strong collaboration across functional areas
  • Work cross-functionally to coordinate the relevant and timely exchange of information and materials to support clinical trial deliveries
  • Oversee the development of clinical trial project timelines and ensure communication and understanding of risks and challenges; establish plans and monitor metrics; ensure that timelines are accurate and comprehensive
  • Proactively manage clinical trial outsourced partners, including identification of risk, to ensure trial deliverables and performance goals are met
  • Maintain daily partnership with CRO counterpart; review and identify potential issues or problems with the sites and communicate/escalate to clinical leadership
  • Collaborate with CRO to keep the clinical study database current and accurate
  • Proactively manage project scope and change orders, for clinical trial operations
  • Additional duties and responsibilities as required
Desired Qualifications
  • Biotechnology experience is a plus
Tango Therapeutics

51-200 employees