Clinical Research Manager

RevBio, Inc. is a medical device company revolutionizing bone repair with its innovative TETRANITE® regenerative bone adhesive. Currently in seven FDA-approved clinical trials, TETRANITE® provides superior wet-field adhesion, rapid mechanical stability, and facilitates bone growth during the natural remodeling process. Bioengineered for applications in neurosurgery, orthopedics, and dentistry, this pioneering “bone glue” addresses a $10 billion market. Aiming for commercialization by Q3 2027, RevBio’s patented technology demonstrates exceptional performance compared to standard bone fixation methods, promising optimized patient outcomes. Role Description 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. Essential Duties and & Responsibilities Interface with RevBio leadership, internal technical teams, and advisory clinical subject matter experts to develop a deep understanding of the clinical, scientific, and operational requirements for successful application of Tetranite in each indication under investigation. Lead the planning, execution, oversight, and continuous improvement of clinical studies across multiple indications and geographic regions. Oversee study startup, site activation, enrollment progress, study conduct, and closeout activities to ensure alignment with protocol, timelines, budget, and regulatory requirements. Provide oversight of site training on study protocols, investigational product use, and applicable Instructions for Use (IFU), ensuring consistency and quality across all participating sites. Oversee data collection progress, monitoring activities, protocol compliance, and issue escalation to ensure high‑quality study execution. Review study metrics, site performance, monitoring findings, and data quality trends, and implement corrective actions as needed. Ensure investigators and site personnel are appropriately supported to complete EDC entries, data uploads, query resolution, and required study documentation in a timely manner. Oversee payment approval processes and confirm alignment between site activity, product delivery, milestone completion, and data submission. Support and contribute to the preparation and submission of clinical trial protocols, informed consent documents, investigator materials, and regulatory documentation required to initiate and maintain clinical studies, including amendments and supplements. Support and contribute to ethics committee and IRB submissions, renewals, supplements, and amendments as applicable. Ensure comprehensive, inspection‑ready documentation is maintained for each clinical site and study, in accordance with RevBio’s Quality Management System and applicable regulations. Provide oversight of internal Clinical Research Associates and/or external CROs, as applicable, to ensure effective site management, monitoring quality, and study execution. Identify study‑level risks and develop mitigation strategies to address operational, compliance, enrollment, or logistical challenges. Lead the investigation and cross‑functional review of adverse events in collaboration with the clinical trial team, including the Principal Investigator, study site personnel, and RevBio representatives, ensuring timely assessment, documentation, escalation, and resolution. Oversee the preparation of adverse event narratives, medical summaries, and adjudication packages for presentation to the Clinical Events Committee (CEC), Data Safety Monitoring Board (DSMB), and other oversight committees, as applicable. Perform other duties as assigned to support RevBio’s clinical development objectives. Essential Education, Skills, Environment Education and Work Experience Bachelor’s degree in Engineering, Biology, Physiology, Life Sciences, or a related field required. Advanced degree preferred. Minimum 5–8 years of experience in clinical research, clinical operations, or medical device/pharmaceutical trials, preferably with increasing responsibility in study management. International study experience strongly preferred. Demonstrated experience managing clinical studies across multiple sites, indications, and/or geographic regions. Experience overseeing site performance, study timelines, and cross‑functional clinical operations activities. Prior experience managing or overseeing Clinical Research Associates, contract research organizations, and/or external vendors preferred. Demonstrated ability to work independently, lead complex initiatives, and manage multiple priorities in a fast‑paced environment. Strong organizational, analytical, and problem‑solving skills with meticulous attention to detail. Excellent oral and written communication skills, with the ability to communicate effectively and confidently with surgeons, investigators, executive leadership, and external partners. Proficient in MS Office Suite (Word, Excel, PowerPoint), Smartsheet, Viedoc or similar EDC platforms, and project management tools. Experience supporting regulatory submissions, IRB/ethics submissions, clinical trial documentation, and inspection readiness activities preferred. Experience contributing to manuscripts, abstracts, conference presentations, and/or grant applications strongly preferred. Comfortable working with high‑risk, early‑stage technologies in a fast‑paced, deadline‑driven start‑up environment. Specialized Knowledge and Skills Strong understanding of clinical trial operations, monitoring oversight, and applicable regulatory requirements across relevant geographic regions, including the United States, Europe, and the United Kingdom. Ability to work effectively in multicultural, multidisciplinary, and cross‑functional environments. Demonstrated success in building and maintaining professional relationships with surgeons, medical professionals, institutions, research collaborators, and external partners. Ability to identify study‑level risks, develop mitigation strategies, and drive solutions to operational and clinical challenges. Familiarity with conference participation, public speaking, investigator engagement, and scientific dissemination. Strong leadership skills, including the ability to influence without direct authority and align internal and external stakeholders around study objectives. Entrepreneurial mindset with the ability to take initiative, think strategically, and adapt quickly in a growing organization. High level of professionalism, judgment, and discretion in representing company interests internally and externally. Willingness and ability to travel extensively across the United States, Europe, and the United Kingdom, up to 50% as required. Commitment to doing what is needed to support a fast‑growing start‑up in achieving key clinical, regulatory, and business milestones. #J-18808-Ljbffr