BS Life Science Job Vacancy at OneOncology | Apply Now for the Regulatory Coordinator Role
OneOncology is seeking a detail-oriented Research Regulatory Coordinator to support clinical research compliance and regulatory processes across its network. This full-time role offers an opportunity to contribute to cutting-edge cancer care by ensuring regulatory adherence, facilitating clinical trial operations, and collaborating with multidisciplinary teams in a fast-paced environment.
- Job Posting: Research Regulatory Coordinator
- Job Requisition ID: R-0000015125
About OneOncology
OneOncology is positioning community oncologists to drive the future of cancer care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer. Our team is bringing together leaders to the marketplace to help drive OneOncology’s mission and vision.
Why join the company?
This is an exciting time to join OneOncology. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, technology, and finance. We are looking for talented and highly motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of community oncologists and the patients they serve.
Job Description
The Research Regulatory Coordinator will collaborate with OneOncology practices to support clinical research across the network by ensuring compliance with regulatory requirements and guidelines for clinical research projects. They will play a crucial role in facilitating regulatory aspects of clinical trials and streamlining regulatory processes within the network.
Responsibilities
- Ensure adherence to regulatory requirements such as FDA regulations, ICH guidelines, and local requirements
- Prepare and submit essential regulatory documents to sponsors/CROs
- Maintain up-to-date regulatory documents and files
- Coordinate regulatory activities for clinical trials
- Stay informed about changes in regulatory requirements
- Maintain relationships within the network to streamline regulatory processes
- Other duties as assigned
Key Competencies
- Strong understanding of clinical trial processes and regulatory requirements
- Attention to detail and organizational skills
- Effective communication and interpersonal skills
- Ability to work independently and collaboratively
Qualifications
- Bachelor’s degree in a relevant field preferred (Life Science)
- 1-2 years of experience in clinical research with a focus on regulatory affairs
- Proficiency in Microsoft Office and clinical trial management systems is preferred
- Certification in clinical research is a plus
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