Aura is on a mission to create a safer internet. In a world where our lives are increasingly online, Aura’s category-defining suite of intelligent digital safety products help millions of customers protect themselves against digital threats, and that number is growing rapidly. This is an exciting phase at Aura, and our team of over 400 people worldwide is guided by a leadership slate that’s successfully grown startups into multi-billion dollar organizations.
Come build with us!
About the Role:
Aura seeks to transform the way we approach and promote online safety for youth. In a time where children and adolescents face a relentless barrage of online threats (eg., ubiquity of social media, cyberbullying, predators, scams, etc.), Aura is building next generation products and tools that will make it easier for kids to navigate the online world and help build healthy online behaviors.
To achieve these goals, we are looking to add a Manager of Clinical Projects to our team. In this new position, you’ll provide operational leadership for a range of new clinical and scientific initiatives. You’ll also manage several new clinical research projects, as well as work with other team members to support ongoing scientific activities. Finally, you’ll be instrumental in facilitating cross-functional collaboration among Medical/Scientific partners, Product, Engineering, and Data Science teams.
Day to Day:
- Manage and oversee operational aspects of all ongoing research efforts
- Manage regulatory aspects of new and ongoing projects, including IRB submissions/management, clinicaltrials.gov registration, etc.
- Work with any external partners/sites/vendors that might be participating as part of clinical studies
- Support clinical partners across range of activities - literature reviews, manuscript prep, conference submissions
- Work with clinical directors to liaison with other functional groups to help drive results and progress
What you bring to the table:
- BS/BA required
- 3-5 years experience managing clinical research projects
- Experience working with local and central IRBs
- Experience developing informed consent documents/preparing research protocols
- CITI certified
- Experience with manuscript preparation, literature review, and conference abstract preparation/submission
It would be great if you also had:
- Masters degree in clinical science or clinical research
- Experience in industry setting; experience in health tech/product development
- Experience with medical/technical writing, budget management a bonus, but not required
Aura is committed to offering a generous package to support our employees in all aspects of their life in and out of work. Our packages offer competitive pay, generous health and wellness benefits, retirement savings plans, parental leave and much more! Pay range for this position is $100,000 - $130,000 but may vary depending on job-related knowledge, skills, experience and location.
Aura is proud to be an equal employment workplace. All qualified applicants will be considered for employment without regard to, and will not be discriminated against based on race, color, ancestry, national origin, religion, age, sex, gender, marital status, sexual orientation, gender identity, disability status, veteran status, or any protected category. Beyond equal employment opportunity, Aura is committed to being an inclusive community where all feel welcome.
Aura is dedicated to providing an accessible environment for all candidates during the application process and for employees during their employment. If you need accessibility assistance and/or a reasonable accommodation due to a disability, please let your Talent Acquisition Partner know.
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