CAREERS

Clinical Trials Specialist / Product Leader

Posted on - 08 Sep 2025
  • Location: India (Remote/Hybrid options available)
  • Position: Full-time

About ThinkBio.Ai®

ThinkBio.Ai® is at the forefront of revolutionizing drug development through cutting-edge software and artificial intelligence. We are building intelligent platforms designed to streamline and optimize the entire clinical trial lifecycle. Our mission is to help bring new therapies to patients faster by making clinical research more efficient, predictive, and data-driven. We are a dynamic and innovative team of scientists, engineers, and entrepreneurs passionate about changing the future of medicine.

Job Summary

We are seeking a highly experienced Clinical Trials Specialist with a background in pharmaceuticals or a Contract Research Organization (CRO) to join our product development team. This is a unique opportunity to step out of the traditional clinical operations role and apply your deep domain expertise to shape the next generation of clinical trial software. You will serve as the subject matter expert, ensuring our Al platforms are built on a solid foundation of real-world clinical research principles and address the most pressing challenges in trial design and execution.

Key Responsibilities

  • Subject Matter Expertise: Act as the primary internal consultant on all aspects of clinical trial design, planning, and protocol development.
  • Product Development Collaboration: Work closely with software engineers, data scientists, and product managers to translate complex clinical trial concepts into functional software requirements and Al model features.
  • Protocol & Design Input: Provide expert review and guidance on trial protocols, study designs (e.g., adaptive trials, decentralized trials, basket trials), and endpoint selection to inform the logic to automate the workflows of our platforms.
  • Feature Validation: Test and validate new software features and Al-driven recommendations to ensure they are clinically sound, compliant, and user-friendly for research professionals.
  • Content & Algorithm Curation: Assist in curating, extracting and, structuring clinical data from scientific literature, and regulatory guidelines to train and refine our Al models.
  • Market & User Insights: Stay abreast of industry trends, regulatory changes (e.g., ICH, CDSCO), and the evolving needs of clinical research professionals to guide product strategy.

Required Qualifications & Experience

  • Educational Background: A degree in Life Sciences, Pharmacy, Medicine, or a related field is required. An advanced degree (Masters, PhD, PharmD) is highly preferred.
  • Industry Experience: A minimum of 7-10 years of hands-on experience working within a pharmaceutical company or a CRO.
  • Core Expertise: Proven, significant experience in the design and development of clinical trial protocols across different therapeutic areas and phases (Phase I-IV). Must have prepared and submitted clinical trial-enabling documents
  • Regulatory Knowledge: Deep understanding of the end-to-end clinical trial process, Good Clinical Practice (GCP), and international/local regulatory guidelines (e.g., ICH-GCP, FDA, EMA, CDSCO).
  • Analytical Mindset: Strong analytical skills with the ability to deconstruct complex clinical processes into logical steps.

Desired Skills

  • Passion for technology and innovation in the life sciences sector.
  • Familiarity with the software development lifecycle or experience working with technology teams is a huge plus.
  • Exposure to or a keen interest in learning Artificial Intelligence, Machine Learning, and data analytics.
  • Excellent communication and interpersonal skills, with the ability to articulate complex scientific concepts to a non-scientific audience.
  • A proactive, problem-solving mindset and the ability to thrive in a fast-paced, collaborative startup environment.

What We Offer

  • The opportunity to be a key player in a cutting-edge HealthTech company.
  • A unique role that bridges clinical science with technology and Al.
  • Competitive salary, benefits, and flexible working arrangements.
  • A collaborative and innovative work culture where your expertise will directly impact the product and the industry.

How to Apply

Interested candidates are invited to send their resume and a brief cover letter explaining their experience in clinical trial design and their interest in technology to :[email protected]