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Research Analyst (Remote)

Tilda Research
Full-time
Remote
India and United States
AI / Machine Learning

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.
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