Curebase
Curebase

Principal Investigator, Oncology

This job is no longer available and isn't accepting applications.

Curebase is seeking a Principal Investigator (Oncology) who will oversee oncology  clinical research studies enabled by our decentralized clinical trial platform. 

About the role

The Principal Investigator (Oncology) is responsible for ensuring that all research team members have appropriate education, training, and qualifications to assume delegated study tests. Principal Investigator is responsible for ensuring that the conduct of the study is compliant with federal and industry guidance and regulations. Principal Investigators manage Phase 1 – Phase 4 studies, with demonstrated decision-making capabilities. They will also engage with the sponsor’s monitor to discuss findings and ensure timely correction and documentation of any identified issues.

The administrative structure of investigational sites under the decentralized site model requires a nontraditional approach. The Principal Investigator will be responsible for the oversight of trial conduct at one or more facilities where participants are located. Since the facilities may not be in close proximity, oversight will be provided in accordance with a well-laid-out Decentralized Clinical Trials Oversight Plan.

This is a fully remote position, where the oversight for sub-investigators, research coordinators, research nurse practitioners, etc. is provided over email, phone, video conferencing, etc. This will be a temporary contract/project based role and you will be compensated for your time spent on study-specific duties.

What you’ll do

  • Oversee Phase 1 – Phase 4 oncology clinical studies
  • Ensure study compliance on all clinical trials/studies according to International Conference on Harmonization-Good Clinical Practice (ICH-GCP), local regulations, and the study protocol
  • Provide clinical oversight and ensure quality of decentralized clinical studies.
  • Meet with study-assigned monitors at regular intervals
  • Train sub-investigators and study personnel on protocol and protocol-specific procedures
  • Participate and engage in driving the delivery of study targets, such as participant recruitment, enrollment and retention

About you

  • Active MD/DO License in good standing
  • Willing/able to obtain multi-state licensure as needed
  • Board certification (any): Medical Oncology, Pathology, Hematology, Internal Medicine

Major pluses

  • Prior clinical research experience (Industry-sponsored preferred)
  • Previous telemedicine, or remote clinical study oversight experience

About Curebase

Curebase is reinventing decentralized clinical trials to help the vast majority of potential patients that currently cannot access clinical research. Our vision is that any patient, no matter where they are located, should be able to participate in clinical trials at home and with their own doctors. This is made possible through a unique suite of tools Curebase’s has designed to engage patients in clinical trials across all settings, be it at home, at their local clinic, or other places in their community.  

This starts with Curebase’s leading decentralized clinical trial software platform that is an all-in-one, purpose built eClinical software system, with every tool needed to manage and collect data for decentralized clinical trials. This includes ePRO, eCOA, eConsent, Telemedicine, and much more. Curebase also offers a virtual research site, complete with virtual investigators, research coordinators, mobile nursing, and other healthcare staff that administer care to patients where convenient for them, just like any other research site, but with the ability to stand up anywhere and with greater patient convenience and reach. Notably, Curebase is the pioneer of the “BYOP” or Bring Your Own Physician model, allowing patients to use their own doctors to participate in clinical trials. 


We are reinventing a $45B market, enabling drug and device companies to increase the volume, quality, and speed of data collection regardless of patients’ physical location. COVID-19 tailwinds have created massive demand for telemedicine and home-based trials, with two new FDA guidance letters and industry-wide adoption of remote remote research that will only accelerate in the years to come. You can learn more about Curebase and our next stage of growth in Crunchbase, Fierce Biotech, and MedCity News!

Not sure you qualify?

Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Curebase we are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles.

Curebase provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

No longer accepting applications

This job is no longer available