Psychiatrist- Sub Investigator
Our mission
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.
Our impact speaks for itself: 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.
What's it like to work here?
When you join us, you’ll experience:
High-Impact, Mission-Driven Work: Lindus is disrupting an outdated industry, giving you the chance to directly improve patients’ lives and see tangible results from your work.
Fast-Paced Growth & Ownership: We recognise hard work and outcomes over anything else. You’ll take on real responsibility, work across different areas, and actively shape the company’s success.
Collaborative, No-Ego Culture: Work with smart, driven people in a supportive and informal environment. At Lindus we break down silos, fun is a core value, and creativity is encouraged.
Ready to power biology's century? We'd love to hear from you.
About the role
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.
About you
We’d like to hear from you if…
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
You belong here! If your experience and interests match with some of the above, we want you to apply.
What you’ll focus on
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
What we offer
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
Our hiring process
Initial conversation with Cam, our Medical Talent Partner (20 minutes)
Technical interview with Luke, our VP of Medical (30 minutes)
We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus carefully before responding. We will never ask for your financial information over email.
We are an equal opportunity employer committed to building a diverse and inclusive workforce. We evaluate all candidates based solely on their skills, experience, and qualifications relevant to the role. We do not discriminate on the basis of race, ethnicity, religion, gender, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected status
Apply To This Job
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.
Our impact speaks for itself: 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.
What's it like to work here?
When you join us, you’ll experience:
High-Impact, Mission-Driven Work: Lindus is disrupting an outdated industry, giving you the chance to directly improve patients’ lives and see tangible results from your work.
Fast-Paced Growth & Ownership: We recognise hard work and outcomes over anything else. You’ll take on real responsibility, work across different areas, and actively shape the company’s success.
Collaborative, No-Ego Culture: Work with smart, driven people in a supportive and informal environment. At Lindus we break down silos, fun is a core value, and creativity is encouraged.
Ready to power biology's century? We'd love to hear from you.
About the role
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.
About you
We’d like to hear from you if…
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
You belong here! If your experience and interests match with some of the above, we want you to apply.
What you’ll focus on
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
What we offer
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
Our hiring process
Initial conversation with Cam, our Medical Talent Partner (20 minutes)
Technical interview with Luke, our VP of Medical (30 minutes)
We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus carefully before responding. We will never ask for your financial information over email.
We are an equal opportunity employer committed to building a diverse and inclusive workforce. We evaluate all candidates based solely on their skills, experience, and qualifications relevant to the role. We do not discriminate on the basis of race, ethnicity, religion, gender, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected status
Apply To This Job