Physician Investigator

2 weeks ago

Houston, United States Axsendo Clinical Full time
Job DescriptionJob DescriptionSalary: $200-$250/hr

The Role: Become a Physician Investigator within the Axsendo Clinical Research Network


Here at Axsendo Clinical Research (ACR), we streamline the research process, empowering physicians to drive innovation and outcomes through advanced clinical research, without the administrative, financial, or operational complexities of managing it on their own.


We're expanding our network of clinical research sites, specializing in Cardiology, Endocrinology, Gastroenterology, Neurology, Metabolic Disease, Vaccines and Medical Devices  and seeking enthusiastic physicians eager to offer innovative care options to patients in their local communities. Our physician partners will play a crucial role in conducting clinical evaluations of patients for specific studies, ensuring adherence to protocols, overseeing study conduct, and ensuring patient safety. As an Investigator, you will be supporting cutting edge research and industry leading projects, impacting and improving health outcomes.


This is an opportunity to conduct clinical trials with Axsendo Clinical Research where ACR provides the physicians with full support staff, industry standard systems and processes, as well as a full business development team so you can focus on what you do best


Responsibilities:


As a Physician Investigator, your responsibilities involve pivotal tasks in clinical trials, including but not limited to:

  • Comprehensive training in relevant research protocols, specimen collection, regulatory compliance, and administrative protocols.
  • Attendance at Pre-Site Qualification and Site Initiation Visits
  • Completion of study-specific training.
  • Thoroughly informing and engaging patients about clinical trial participation opportunities.
  • Conducting detailed examinations and assessments of trial participants.
  • Active participation in mandatory study team meetings.
  • Execution of all necessary Research Project documentation and agreements.
  • Documenting any observed side effects or adverse reactions.
  • Compliance with FDA and Sponsor-directed requirements, including Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training.
  • Maintaining board certification in the specified specialty.
  • Ensure that the safety and well-being of all participants

Your Credentials:

  • Medical Doctor (MD) or Doctor of Osteopathic Medicine (DO) degree.
  • Active Medical License in good standing in Texas and/or Arizona.
  • Board Certification in Cardiology, Endocrinology, Family Medicine/Internal Medicine, Gastroenterology, Neurology, or Pulmonology.
  • Prior clinical research experience is advantageous but not required.
  • Proficiency in both English and Spanish is advantageous.


Locations: Houston, TX


Travel: Limited to commuting to and from the research site.


Highlights

  • Create an additional revenue stream for yourself and your practice without any upfront cost.
  • Bring new, cutting-edge therapies to your patients. Provide new care options for your patient population.
  • Elevate your personal brand and grow your experience.

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