About the Company
- The Tilda team has held various roles across all parts of clinical trial management over the years.
- They noticed that clinical trial site management was often inefficient, unclear, slow, and not working well.
- Their drive to find a solution, and their belief in technology to connect things, brought them together to build a new network of clinical trial sites, supported by their technology platform.
- By putting money into workflow automation, centralization, and data connection across their sites, they can achieve better study conduct results and success for their physicians, pharma, and CRO partners.
- Tilda is a San Francisco based startup, supported by top venture funds and industry leaders.
- They are inviting passionate people who agree with their goal to join their team of world-class engineers, data scientists, and clinical operations experts to rethink the structure for modern health innovation.
Responsibilities
- Communicate with biotechnology and pharma clients over email and create specific regulatory and supporting documents as needed.
- Manage, fact-check, and enter data across various research related systems.
- Answer any regulatory document requests by looking up the information in their local storage and sending emails back.
- Organize documentation, and get electronic signatures from the right people if needed.
- Handle any administrative tasks that come up.
Requirements
- MBA required.
- Excellent internet connection at home with video conference ability.
- Ability to work during late hours (half-time overlap with US time zone).
- Excellent spoken and written English communication.
- Ability to learn and use new technology and software.
- Attention to detail.
Preferred Qualifications (Nice to Have)
- Some understanding of basic medical terminology is helpful.
- Ability to learn from online sources and get up to speed on various clinical research related topics like IRB interactions, Study Protocols, Delegation of Authority, and inventory logs.