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Biomedical Ops Director / Sr. Management Consultant (Remote)

New York (Fully Remote), NY · Biotech/Pharmaceutical
Biomedical Ops Director / Sr. Management Consultant (Remote)

Work for one of the most dynamic and diverse NexGen fully integrated drug development partners committed to the field of clinical research. With a great leadership team, incredible employee appreciation and undeniable chances to grow – look what we have to offer you! 

*Amazing Pay: $80,000 to $200,000 Base Salary, Plus up t o10% annual bonus and stock equity options.

COMPANY PROFILE:
 
  • Throughout our history, we have partnered with drug and medical device manufacturers to enact innovative change within the CRO space.
  • We strive to deliver a concierge like experience to our partners while demonstrating unmatched flexibility.
  • Supporting local clinical sites with our white-label administration approach and individualized medical technologies, we are liberating the siloed boundaries of research for everyone.
  • Our team consists of proven clinical researchers spanning the medical, scientific, and operations fields built on experience with healthcare professionals, universities, and leading institutions.
  • Alongside drug and device manufacturers, our goal is to enact lasting innovative change in the clinical research landscape, benefiting consumers alike


FEATURES AND BENEFITS:
Highly competitive benefits, salary, profit sharing perform incentives:
  • Be part of an employee-owned company.
  • Remote telehealth at no cost.
  • In/Out Network Coverage
  • Generous Employer Coverage of Health Premiums
  • Plus, Religiously Minded Specialized Plan Options


THE ROLE YOU WILL PLAY:
Seeking “Rockstar” Biomedical Operational Research Candidates for this exciting role of Biomedical Operations Director.

Qualified candidates must have a high level of expertise in biomedical operational research and must also be able to oversee multiple studies remotely. The ideal candidate will also have experience managing multiple programs and people.


BACKGROUND PROFILE:

  • 7+ years of expertise in industry clinical research experience working at a contract research organization or a pharmaceutical company

  • 2 – 4 years or more experience in the oversight of novel oncology and advanced cellular therapeutic protocols

  • 3+ years specifically in Ph I/II Onsite Clinical Trial Monitoring (Complex indications)

  • 1+ years overseeing clinical operations and CRO / vendors

  • ICH-GCP certification, Cybersecurity Awareness, Emotional Focus

  • Master’s degree or MD/PhD in a life or physical sciences discipline from an accredited US institution.
 
It would also be an advantage to have the following:
  • At least one year of mentoring and/or supervising experience of 2-3 people or more
  • Clinical Research Certification (i.e., SoCRA, RAPs, ACRP)

 
The Patriot Group, Inc. (TPGI)
www.thepatriotsgrp.com
Info@thepatriotsgrp.com
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