Careers

Cancer Targeted Technology develops specific imaging agents and personalized therapy for cancer that accurately detect advanced disease, monitor treatment efficacy and improve patient survival and quality of life.

CTT is pioneering the development of novel drug products targeting pivotal enzyme targets in cancer. We are searching for highly qualified individuals who are looking to make a difference in improving people's lives while working in a motivated and enthusiastic start-up environment. CTT offers an exciting opportunity for growth and development and competitive salary.

For more information, please contact: hr@cancertargetedtechnology.com

NEW JOB POSTING:  Medical Consultant - Prostate Cancer  

We are looking for a Medical Consultant who can help develop and articulate a clinical development plan for CTT's chemotherapy programs, and helpp with the submission of an IND and oversee the clinical trial. 

Location

Remote

Key Responsibilities

  • Provide feedback on the translation into clinic using preclinical animal data
  • Participate in discussions on prostate cancer therapy landscape, both preclinical and clinical therapies
  • Advise on content of clinical protocol, investigator brochure, and other clinical documents as needed
  • Review and sign off on Data Safety Monitoring Plan
  • Serve on Data Safety Monitoring Board for new compounds
  • As needed, review AE/SAE form sent by clinical study site
    • After review by the primary clinical site, advise sponsor principal investigator whether an AE or SAE is likely an adverse reaction
    • Work with sponsor’s regulatory representative to address requisite steps and direct queries regarding AEs and SAEs
    • Ensure regulatory reporting timelines are met as per the Data Safety Monitoring Plan and FDA regulations in collaboration with the sponsor’s regulatory representative, clinical research associate, program manager, and principal investigator
  • As needed, review safety data collected to advise the Data Safety Monitoring Board and study sponsor on matters related to study dose and dose/regimen
  • Prepare a safety data report at completion of clinical trials for presentation to the FDA to support future clinical trials
  • Be available for interactions with regulatory authorities as needed
  • Be available for phone calls/virtual meetings as needed to discuss clinical trial protocol or strategy
  • Provide feedback on CSRs as needed
  • Provide feedback on design of electronic clinical trial database

Requirements

  • Professional degree - MD 
  • Board certification in medical oncology
  • Extensive knowledge of prostate cancer, current treatment algorithms, and treatment research
  • Knowledge of pharmaceutical drug development and product lifecycle
  • Knowledge of Good Clinical Practices and FDA regulations and guidelines for drug safety and event reporting
  • Strong communication and interpersonal skills

Time Commitment

5-10 hrs of work is expected in 2024, with hours expecting to reach 30- 40    hours per year in 2025 and 2026.

Rate

$250-400/hr dependent on prior experience

Policies

CTT is an Equal Opportunity Employer

Financial Conflict of Interest Policy: PDF