Clinical Research Associate I

Are you ready to work for a more active world?

At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.

Are you just getting started in your clinical career and want a role that makes an impact while giving you hands on experience? Our entry level Clinical Research Associate position will have a direct impact on an array of trials and initiatives in support of our innovative, growing, medical technology company. Our ideal candidate has at least 1 year experience in clinical research or clinical trials, site monitoring, is motivated to learn and grow, and wants to make an impact, this role could be for you!

The Clinical Research Associate (CRA) will participate in the preparation and execution of a variety of clinical research initiatives, including approval trials, post-market activities, registries surveys and other initiatives. The CRA will oversee the progress of clinical research related activities, either independently or in coordination with internal stakeholders and external vendors as required by conducting site evaluation, initiation, interim monitoring, and close out visits to sites to ensure ongoing compliance with applicable regulations, ICH/GCP guidelines, and protocol requirements. The CRA will also facilitate the identification, qualification, and initiation of clinical sites.

Key Responsibilities:

1. Assist Clinical Affairs leadership and team members in developing study-specific investigator/site requirements to enable identification and qualification of potential clinical sites
2. Develop study-specific training for site initiation visits as aligned with Clinical Affairs leadership
3. Assist in the preparation and support of research site qualification and site initiation visits
4. Perform on-site and remote monitoring and study closure activities across multiple protocols
5. Ensure that sites operate in compliance with study protocols, SOPs, ICH/GCP guidelines, and applicable regulations
6. Monitor, track, and support patient enrollment and study progress
7. Ensure the timely, accurate, and complete collection and submission of study data
8. 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
9. Maintain and track regular correspondence with sites through email or telephone
10. Proactively identify, address, and resolve issues and problems at the clinical site as they might occur
11. Manage required study documentation through accurate filing in the designed Trial Master File system
12. Prepare monitoring reports
13. Assist in distribution and tracking of regulatory documents
14. Assist Clinical affairs leadership and team members in development of study and site budgets
15. If applicable, facilitate activities to enable payment for sites
16. 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.

Education and Experience (Knowledge, Skills & Abilities)

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Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.