AxoGen Overview

AxoGen (AXGN) is a global leader in innovative surgical solutions for peripheral nerve injuries. AxoGen is focused on the science, development and commercialization of technologies for peripheral nerve regeneration and repair. Peripheral nerves provide the pathways for both motor and sensory signals throughout the body. Every day, people suffer traumatic injuries or undergo surgical procedures that impact the function of their peripheral nerves.  Damage to a peripheral nerve can result in the loss of muscle or organ function, the loss of sensory feeling or the initiation of pain. Injuries to peripheral nerves can significantly impact the patient’s quality of life.

AxoGen's portfolio of products includes Avance® Nerve Graft, an off-the-shelf processed human nerve allograft for bridging severed nerves without the comorbidities associated with a second surgical site, AxoGuard® Nerve Connector, a porcine submucosa extracellular matrix ("ECM") coaptation aid for tensionless repair of severed nerves, AxoGuard® Nerve Protector, a porcine submucosa ECM product used to wrap and protect injured peripheral nerves and reinforce the nerve reconstruction while preventing soft tissue attachments and Avive Soft Tissue Membrane, a minimally processed human umbilical cord membrane that may be used as a soft tissue covering to reduce inflammation and scar tissue formation. Along with these core surgical products, AxoGen also offers AxoTouch Two-Point Discriminator and AcroValTM Neurosensory & Motor Testing System. These evaluation and measurement tools assist healthcare professionals in detecting changes in sensation, assessing return of sensory, grip and pinch function, evaluating effective treatment interventions, and providing feedback to patients on nerve function. The AxoGen portfolio of products is available in the United States, Canada, the United Kingdom and several European and international countries. 

AxoGen maintains its corporate offices in Alachua, Florida.  

AxoGen provides a great work environment that includes a fast-paced innovative team with a strong commitment to restoring quality of life to patients with nerve injuries.

Job Summary

This position will operate as a corporate office based Clinical Research Associate (CRA) who will function as the main point of contact for assigned sponsored and investigator initiated studies. The CRA will perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs) including site GCP compliance, trouble shoot issues and facilitate resolution, and monitor safety at the site.

A qualified clinical research associate will conduct site initiation visits, interim visits, monitoring visits and close-out visits; writing reports or reviewing monitoring reports provided by Contract Research Organizations (CRO).

Job Responsibilities

Principal duties and responsibilities include the following:

  • Ensures compliance with protocol and all regulatory policies, procedures and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions
  • Assist with development and implementation of protocol design, study training documents, study documents, and plan management.
  • Conduct Site Qualification, initiation visits, on-site monitoring visits, co-monitoring visits, and site closure visits of all phases of clinical trials
  • Interfaces with clinical sites/investigators on-site and through off-site administrative site management to ensure compliance with protocols and regulatory compliance
  • Prepares and/or tracks required documentation for clinical sites (contracts, budgets, IRB documentation)
  • Assists with information gathering, literature searches, data analysis, report generation, and creation of presentations
  • Prepares reports of study progress to upper management
  • Assists with the development and maintenance of study databases
  • Participates in in-house and/or external training and educational opportunities to build field expertise

Educational Requirements/Qualifications:

  • Bachelor’s degree in a scientific discipline with 2 years previous clinical research experience
  • Demonstrates the ability to interface with clinical sites/investigators to ensure compliance with protocols and regulatory requirements
  • Ability to read and critically interpret relevant literature. Serve as a resource for clinical knowledge.
  • Oral and written communication skills are essential!
  • Capable of working on clinical monitoring issues of moderate scope
  • Exercises judgment on routine clinical procedures and practices to determine appropriate action
  • Strong interpersonal skills, exceptional organizational and time-management skills
  • Ability to work independently and collaboratively in a team environment
  • Ability to quickly adapt to changes in departmental priorities and goals to meet company strategies and directives
  • Knowledge of GCP/IHC regulatory requirements
  • Must be willing to travel (50% of time)


We are seeking candidates who are AxoGenic, which means:

  • Respect is the foundation for communication and action.
  • Patient safety is our first priority.
  • In being effective stewards of the gift of human tissue.
  • In creating and maintaining a company culture that encourages and rewards honesty, openness, passionate debate – and fun!
  • Individual ownership and empowerment lead to superior team results.
  • The organization, its members and partners must consistently achieve agreed upon results with flexibility and mutual support.
  • Speed is critical!
Qualified candidates click here to submit Cover Letter & Resume