Psychiatrist- Sub Investigator

Lindus Health

About The Position

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.

Requirements

You are a board-certified psychiatrist or physician with substantial psychiatry clinical trial experience. You must hold a 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.
You're GCP-certified with demonstrated clinical research experience and understanding of ICH-GCP guidelines and FDA regulations
You're a dynamic communicator who can credibly champion Lindus Health's approach in client-facing situations
You're responsive, engaged, and bring strategic insights beyond basic protocol execution
You're business-minded with genuine enthusiasm for clinical research innovation

Responsibilities

Champion Lindus Health: Actively participate in bid proposals, represent our values in client-facing situations, and help us win business with your clinical credibility and advocacy
Provide medical oversight: Conduct clinical research activities in accordance with GCP guidelines, supervise investigational product testing, and ensure informed consent and protocol compliance
Ensure participant safety: Monitor and promptly report adverse events, protocol deviations, and any safety concerns throughout all phases of the trial
Manage study documentation: Complete case report forms accurately and timely through our Citrus platform, maintain comprehensive study records, and ensure proper investigational product handling
Collaborate across teams: 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