Green Life Science
Principal Investigator (PI) / Sub-Investigator (Sub-I) – Psychiatry (Remote, Freelance)
Fully Remote (United States) Support needed across
multiple U.S. states Clinicians with multiple active state licenses strongly preferred
Freelance / Independent Contractor Highly flexible scheduling
We are a supporting clinical research organization specializing in
decentralised and virtual clinical trials , with a strong focus on patient-centric, technology-enabled study delivery.
We are seeking
licensed Physicians (MD or DO)
with experience in
psychiatry
to serve as
Principal Investigators (PIs) or Sub-Investigators (Sub-Is)
on upcoming and ongoing decentralised clinical trials.
This is a
fully remote role , ideal for clinicians looking to
expand their clinical research experience , gain exposure to innovative trial models, and work with
maximum flexibility
alongside other clinical commitments.
Key Responsibilities Conduct
remote study visits and telehealth consultations
with clinical trial participants Serve as
Principal Investigator or Sub-Investigator , as appropriate to study requirements Perform protocol-required psychiatric assessments and evaluations Ensure
patient safety , medical oversight, and protocol compliance Review and document adverse events, concomitant medications, and clinical outcomes Collaborate remotely with study coordinators, sponsors, and CRO clinical teams Maintain accurate and timely
electronic source documentation (eSource) Adhere to
ICH-GCP , FDA regulations, and applicable state medical requirements
Required Qualifications MD or DO
with completed residency training Board-certified or board-eligible in Psychiatry Active, unrestricted
medical license in at least one U.S. state Ability to provide care via
telemedicine Strong communication skills and comfort working in a fully remote environment
Preferred Qualifications Multiple active U.S. state medical licenses
(the more licenses, the greater the opportunity for additional work) Prior experience as a
Principal Investigator or Sub-Investigator Previous exposure to
clinical trials , clinical research, or decentralised studies Experience with psychiatric clinical scales and assessments Familiarity with electronic medical records and eClinical systems
Work Model & Flexibility 100% remote
– no on-site visits required Extremely flexible scheduling
– work around your existing clinical or personal commitments Choose when and how much you work based on
study availability and licensure coverage Opportunity to increase workload as new studies launch
Why Join Us Gain hands-on experience in
decentralised clinical trials Expand your
clinical research portfolio
without disrupting your primary practice Work with innovative study designs and digital health technologies Ideal opportunity for psychiatrists seeking
flexible, meaningful freelance work Competitive per-visit or per-study compensation (study dependent)
Additional Information This role is open to candidates across
most U.S. states Candidates with
multi-state licensure
will be prioritised for higher study volume All training related to study protocols and systems will be provided
Fully Remote (United States) Support needed across
multiple U.S. states Clinicians with multiple active state licenses strongly preferred
Freelance / Independent Contractor Highly flexible scheduling
We are a supporting clinical research organization specializing in
decentralised and virtual clinical trials , with a strong focus on patient-centric, technology-enabled study delivery.
We are seeking
licensed Physicians (MD or DO)
with experience in
psychiatry
to serve as
Principal Investigators (PIs) or Sub-Investigators (Sub-Is)
on upcoming and ongoing decentralised clinical trials.
This is a
fully remote role , ideal for clinicians looking to
expand their clinical research experience , gain exposure to innovative trial models, and work with
maximum flexibility
alongside other clinical commitments.
Key Responsibilities Conduct
remote study visits and telehealth consultations
with clinical trial participants Serve as
Principal Investigator or Sub-Investigator , as appropriate to study requirements Perform protocol-required psychiatric assessments and evaluations Ensure
patient safety , medical oversight, and protocol compliance Review and document adverse events, concomitant medications, and clinical outcomes Collaborate remotely with study coordinators, sponsors, and CRO clinical teams Maintain accurate and timely
electronic source documentation (eSource) Adhere to
ICH-GCP , FDA regulations, and applicable state medical requirements
Required Qualifications MD or DO
with completed residency training Board-certified or board-eligible in Psychiatry Active, unrestricted
medical license in at least one U.S. state Ability to provide care via
telemedicine Strong communication skills and comfort working in a fully remote environment
Preferred Qualifications Multiple active U.S. state medical licenses
(the more licenses, the greater the opportunity for additional work) Prior experience as a
Principal Investigator or Sub-Investigator Previous exposure to
clinical trials , clinical research, or decentralised studies Experience with psychiatric clinical scales and assessments Familiarity with electronic medical records and eClinical systems
Work Model & Flexibility 100% remote
– no on-site visits required Extremely flexible scheduling
– work around your existing clinical or personal commitments Choose when and how much you work based on
study availability and licensure coverage Opportunity to increase workload as new studies launch
Why Join Us Gain hands-on experience in
decentralised clinical trials Expand your
clinical research portfolio
without disrupting your primary practice Work with innovative study designs and digital health technologies Ideal opportunity for psychiatrists seeking
flexible, meaningful freelance work Competitive per-visit or per-study compensation (study dependent)
Additional Information This role is open to candidates across
most U.S. states Candidates with
multi-state licensure
will be prioritised for higher study volume All training related to study protocols and systems will be provided