[Hiring] Psychiatrist- Sub Investigator @Lindus Health

Role Description

We're looking for a dynamic Sub-Investigator to support a live US clinical trial while serving as an active advocate and advisor for Lindus Health. This is an immediate need for an active study, combining hands-on protocol execution with strategic advisory contributions to help position Lindus Health competitively in the US market.

Unlike traditional Sub-Investigator positions, this role requires someone who can articulate and champion Lindus Health's innovative approach to clinical trials, contribute meaningfully to bid proposals and client presentations, and serve as a credible voice for our capabilities in the market.

Qualifications

• Board-certified psychiatrist or physician with substantial psychiatry clinical trial experience.
• Current, unrestricted medical license (MD, DO, or equivalent) in at least one of the following states: Ohio, Georgia, Michigan, New Jersey, Washington, Massachusetts, Indiana, Maryland, Missouri, Wisconsin, or Colorado.
• GCP-certified with demonstrated clinical research experience and understanding of ICH-GCP guidelines and FDA regulations.
• Dynamic communicator who can credibly champion Lindus Health's approach in client-facing situations.
• Responsive, engaged, and brings strategic insights beyond basic protocol execution.
• Business-minded with genuine enthusiasm for clinical research innovation.

Requirements

• Actively participate in bid proposals, represent our values in client-facing situations, and help us win business with your clinical credibility and advocacy.
• Conduct clinical research activities in accordance with GCP guidelines, supervise investigational product testing, and ensure informed consent and protocol compliance.
• Monitor and promptly report adverse events, protocol deviations, and any safety concerns throughout all phases of the trial.
• Complete case report forms accurately and timely through our Citrus platform, maintain comprehensive study records, and ensure proper investigational product handling.
• Work closely with Clinical Operations, Product, and Commercial teams while responding promptly to all information requests and maintaining transparent communication.

Benefits

• Make an impact across all areas of our business and fix one of the world’s most broken industries.
• Work on high-impact clinical trials.
• Collaborate with industry-leading medical professionals and sponsor teams.
• Enjoy flexible scheduling and project variety.
• Competitive contractor rates.
• Leverage our established infrastructure and resources.
• Work with a stable, well-funded organisation.
• Contribute your expertise to meaningful research.
• Receive comprehensive support from our medical team.
• The flexibility of working as a contractor.

Company Description

We're powering biology's century with radically faster, more reliable clinical trials. Every new treatment needs clinical trials to prove safety and efficacy, but today's infrastructure is stuck in the past—driving up cost, causing delays, and ultimately meaning new treatments don’t get to patients. We're fundamentally changing that—not just being a "better CRO," but transforming how people think about developing new treatments, so patients can access breakthrough treatments faster.

Since March 2021, we've powered 100+ clinical trials involving tens of thousands of patients. We recently raised a $55M Series B from Balderton Capital, alongside backing from Creandum, Firstminute, Seedcamp, and Visionaries.