Research Analyst (Remote)

Tilda Research; San Francisco (CA); Remote; USD 60,000 - 80,000; Full time

Job summary

A clinical research technology firm is seeking a Research Analyst who can work remotely. This role requires an MBA and excellent English communication skills. Responsibilities include interacting with clients to create regulatory documentation, managing research data, and responding to document requests. Candidates should be detail-oriented and prepared to learn new technologies, with the ability to overlap work hours with US time zones. The position offers a chance to contribute to innovative clinical trial solutions.

Qualifications

• MBA required.
• Excellent spoken and written English communication skills.
• Ability to work during late hours (1/2-time overlap with US time zone).

Responsibilities

• Interact with clients over email and create regulatory documentation.
• Manage, fact-check, and enter data across research-related systems.
• Respond to regulatory document requests by searching local repository.
• Organize documentation and get e-Signatures when necessary.
• Handle any administrative tasks as required.

Skills

Interpersonal skills

Email communication

Document parsing

Attention to detail

Ability to learn new technology

Education

MBA

Job description

About the Role

We are looking for candidates with excellent interpersonal and english communication skills, who can work in a Research Analyst role for our company. We are based in India and USA and this position will be fully remote, working from home.

You will have excellent email communication, document parsing and review skills to understand various clinical research related tasks and requirements. Some understanding of basic medical terminology is helpful, but not required. You will be a quick learner, with the 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, inventory logs, etc.

We will provide some domain and job specific context, but we expect you to be able to learn on the job and be self‑motivated to perform.

Responsibilities

• Interact with biotechnology and pharma clients over email and create specific regulatory and supporting documentation as required
• Manage, fact‑check and enter data across various research related systems
• Respond to any regulatory document requests by looking up the info in our local repository and sending emails back
• Organize documentation, and get e‑Signatures from respective parties if required
• Any administrative tasks which might come up

Requirements

• MBA required
• Excellent internet connection at home with video conference capability
• Ability to work during late hours (1/2‑time overlap with US time zone)
• Excellent spoken and written english communication
• Ability to learn and use new technology and software
• Attention to detail

About Tilda

The Tilda team has held various roles across all aspects of clinical trial management over the years. And during this time, we have often asked questions around clinical trial site management being so… inefficient, opaque, slow and broken. Our drive to find a solution, and our belief in technology to bridge the gap brought us together to build a new, ground‑up network of clinical trial sites, enabled by our technology platform. By investing in workflow automation, centralization and data integration across our sites, we are able to drive better study conduct metrics, and success for our physicians, pharma and CRO partners. We are inviting passionate individuals who can relate to our mission, to join our team of world‑class engineers, data scientists and clinical operations experts to reimagine the infrastructure for modern health innovation. We are a San Francisco based startup, backed by leading venture funds and industry leaders.