Bioventus · 1 day ago
Clinical Research Associate I
Durham, NC
Full-time
Hybrid
Entry, Mid Level
2+ years expBioventus is dedicated to developing its people and fostering a diverse team to help patients enjoy active lives. The Clinical Research Associate I will participate in various clinical research initiatives, overseeing compliance with regulations and facilitating site evaluations and monitoring activities.
Health CareHealth DiagnosticsMedical Device
Responsibilities
Assist Clinical Affairs leadership and team members in developing study-specific investigator/site requirements to enable identification and qualification of potential clinical sites
Develop study-specific training for site initiation visits as aligned with Clinical Affairs leadership
Assist in the preparation and support of research site qualification and site initiation visits
Perform on-site and remote monitoring and study closure activities across multiple protocols
Ensure that sites operate in compliance with study protocols, SOPs, ICH/GCP guidelines, and applicable regulations
Monitor, track, and support patient enrollment and study progress
Ensure the timely, accurate, and complete collection and submission of study data
Liaise with investigators and staff prior to study initiation to ensure all aspects of study are understood, confirm appropriateness of IRB and ensure that all documentation required to initiate study is complete
Maintain and track regular correspondence with sites through email or telephone
Proactively identify, address, and resolve issues and problems at the clinical site as they might occur
Manage required study documentation through accurate filing in the designed Trial Master File system
Prepare monitoring reports
Assist in distribution and tracking of regulatory documents
Assist Clinical affairs leadership and team members in development of study and site budgets
If applicable, facilitate activities to enable payment for sites
Hold oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance, policies and procedures and internal controls applicable to their role
Qualification
Required
Minimum 4 year degree in Health-related field (e.g., nursing, physical therapy, public health)
Registered Nursing certification or equivalent licensure from an appropriately accredited institution will also be considered
Demonstrated understanding of medical terminology
Demonstrated ability to attain and maintain a working knowledge of current ICH/GCP guidelines and application in accordance with Standard Operating Procedures (SOPs) as applicable; may contribute to the development and/or review of relevant SOP's
Good oral and written communication skills, with the ability to communicate effectively with medical personnel, including surgeons and surgical staff
Excellent attention to detail with demonstrated organizational and time management skills
2-5 years industry experience
Computer literate and proficient in MS Office
Preferred
ACRP or similar certification highly desirable
Knowledge of electronic capture preferred
Company
Bioventus
Bioventus delivers clinically proven, cost-effective products that help people heal quickly and safely.
1001-5000 employees
H1B Sponsorship
Bioventus has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (6)
2024 (5)
2023 (2)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
$827MKey Investors
Wells Fargo
2025-07-31Post Ipo Debt· $400M
2022-04-26Post Ipo Debt· $415M
2021-02-10IPO
Leadership Team
Mark Singleton
Senior Vice President and Chief Financial Officer
M
Miguel O. Beltran-Delgado
Senior Vice President Operations
Recent News
2025-12-09
Company data provided by crunchbase