Background

TrialSpark is a technology company that brings new medical treatments to patients faster by reimagining the clinical trial process. We’re fundamentally changing how clinical trials are run, rethinking the trial process both from a technology and operational perspective. To achieve this, we’re bringing together talent from top technology, CRO, and biopharma companies to work side by side.

Job Description

The Medical Director will be responsible for providing clinical support to our operational teams. They will take active roles in our network/PI growth and engagement strategies, as well as work closely with our research coordinators and be a close advisor on clinical operations.

Responsibilities

• Medical advisory
  • Protocol review - advise on recruitment and execution feasibility
  • Clinical go/no-go decision for Bid decision
    
  • EHR mining strategy definition and structure
• Patient Recruitment
  • Input into marketing brief, helping to educate on condition and patient population 
  • Creation of new channels recruitment strategies - i.e. creative ideas/channels for where we can find patients
  • Define organization structure and hiring roadmap to execute against our strategy
    
• Training
  • Clinical training for the TrialSpark team including but not limited to overviews of specific disease areas, drug MOA
    
• Network engagement
  • Physician marketing / recruitment support
  • Participating in meetings with new physician groups and health systems
• Trial operations
  • SMO services
    • Clinical support for CRCs - questions, escalations, etc.
    • Clinical evaluation of clinical ops processes and trainings
    • Clinical and Medical oversight of study activities (supporting on SAEs, etc).
  • Central TrialSpark site oversight
    • Conducting patient screenings and visits (if appropriate)
    • Oversight of other physician activities at the central TrialSpark site
• Regulatory
  
  • Lab director for CLIA
    

About you

• Practice experience (4+ years):
• Preferably in a speciality related to our priorities, but flexible
• Should be able to confidently speak to other conditions outside of specialty
• Written and verbal communication:
• Experience serving as a PI for clinical trials
• In-depth knowledge of GCP for PIs and trial sites
• Should have experience working on structured projects, ideally from a consulting or non-practice role
• Should be able to take complex requirements and structure them into a plan of execution
• Should demonstrate reliability and high level of organization
• Should demonstrate clear, organized written communication abilities
• Should be a strong verbal communicator to both patients and PIs
• Execution and project management
• GCP/CT knowledge (research experience)

Bonus points for

• BioPharma experience (2+ years):
• Experience working in some capacity at a BioPharma or CRO
• Experience in tech/management consulting

You will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.