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TriloDocs

Mid-Level Python Developer

Remote

United kingdom

Mid level

Full Time

04-12-2025

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Skills

Communication Python Kanban Scrum Agile methodologies Problem-solving Attention to detail Effective Communication Software Development Agile

Job Specifications

About TriloDocs

TriloDocs is a growing company at the intersection of technology and life sciences. We help pharma and healthcare organizations transform scientific data into clear, structured documents. Our team is passionate about creating intuitive, reliable tools that make a real difference.

The Role

We're looking for a Mid-Level to Senior Python Developer with a strong STEM background — someone who can not only write clean, effective code but also understand and work with scientific tables and datasets. You’ll contribute to the design and development of scalable, secure software solutions, and collaborate closely with other developers, product managers, and domain experts.

Responsibilities

Write clean, maintainable Python code.
Build and improve backend systems and APIs.
Work with structured scientific and clinical data.
Participate in code reviews, testing, and documentation.
Collaborate in Agile teams using Scrum or Kanban.
Stay up-to-date with best practices and emerging technologies.

Qualifications

At least 2 years of experience as a developer in a B2B environment.
Bachelor's or Master's degree in a STEM field.
Solid understanding of Python fundamentals.
Understanding of software development life cycle and Agile methodologies.
Excellent analytical and problem-solving skills with attention to detail.
Effective communication and collaboration skills.
Ability to work independently and as part of a team.
Knowledge of the Pharma or healthcare industry is a plus.

What we offer

A chance to join a driven team making a real-world impact.
Flexible, remote-first work environment.
A startup environment with global reach — based in London but working across borders.
Flat hierarchies and direct communication.

About the Company

TriloDocs is an AI tool that generates an initial draft of a Clinical Study Report (CSR). Pulling data from all source documents, the 1st draft report accurately reflects the input material (clinical protocol, statistical analysis plan, and the data tables and figures), leaving the crafting of the messages to the medical writer and the clinical team. The output is a Word file in the Transcelerate template (adaptable on request). Methods are generated from protocol, amendments, and Statistical Analysis Plan. Results are gene... Know more