Current Open Positions at RevBio and RevBio Animal Health
The Clinical Research Manager will lead and support clinical operations across multiple indications and geographic regions, including the United States, Europe, and the United Kingdom. This individual will be responsible for the overall operational management of clinical studies, including planning, execution, oversight, and cross-functional coordination, to ensure trials are conducted in compliance with applicable regulations, study protocols, timelines, and corporate objectives.
In addition to overseeing day-to-day study operations, the Clinical Research Manager will play a key role in developing and maintaining strategic relationships with surgeons, clinical staff, hospital administrators, and research partners. These relationships will support collaboration opportunities, site identification and qualification, and recruitment of new Principal Investigators and study centers. The role may include oversight of internal Clinical Research Associates and/or external contract research organizations (CROs), with responsibility for ensuring high-quality monitoring, site performance, and consistent study execution.
This role requires a balance of operational leadership and external engagement. The successful candidate will develop a strong knowledge of RevBio’s product portfolio and clinical applications and will be responsible for ensuring sites are appropriately trained and supported on study protocols, investigational use requirements, and study procedures. They will oversee study-specific compliance, data collection progress, site performance, monitoring activities, and issue escalation and resolution, while supporting regulatory submissions and facilitating effective communication between study sites and RevBio headquarters.
The Clinical Research Manager will also represent RevBio at scientific and medical meetings, support the preparation and presentation of clinical and scientific materials, and contribute to manuscripts, abstracts, and grant applications as needed. This individual will be expected to proactively engage with the surgical and research communities to expand RevBio’s clinical network, strengthen the company’s credibility, and support the growth of its clinical efforts in the United States and internationally.
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The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United Kingdom. This individual will work closely with investigative sites, internal team members, and external partners to help ensure that clinical trials are conducted in accordance with study protocols, applicable regulations, Good Clinical Practice, and corporate objectives.
The Clinical Research Associate will play a key role in site management and study execution, including supporting site initiation, training, routine monitoring, and close-out activities as applicable. They will assist in ensuring that sites are properly trained on study protocols, investigational use requirements, and study procedures, and will help monitor adherence to protocol, informed consent requirements, data collection expectations, and reporting obligations. The Clinical Research Associate will also support the review of study data, identification and follow-up of discrepancies or compliance issues, and timely communication of site needs, risks, and study progress to RevBio headquarters.
This role requires strong attention to detail, organization, and communication skills, as well as the ability to build productive working relationships with surgeons, clinical staff, and research coordinators. The Clinical Research Associate will help maintain effective communication between clinical sites and RevBio, support site performance and enrollment efforts, assist with essential study documentation, and contribute to inspection readiness and overall study quality.
In addition to supporting study execution, the Clinical Research Associate may assist with conference attendance, investigator engagement, clinical material preparation, and other activities that strengthen RevBio’s clinical operations and external relationships. The successful candidate will be expected to develop a detailed understanding of RevBio’s products, clinical studies, and therapeutic applications, and to serve as a reliable operational partner in the advancement of the company’s clinical programs.
APPLY ON LINKEDIN: https://www.linkedin.com/jobs/view/4393563614/