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UpTrials

Principal Investigator - PsychiatristOct 22, 2025Tucson, Arizona, 85704, USAIn Person, Part Time, Contract$150 - $250Salary/HourlyMinimum years of clinical research experience (required)1DescriptionUpTrials is a new platform that helps professionals like yourself get hired faster for relevant clinical research roles. We are partnered with an organization seeking a Principal Investigator (Psychiatrist) to join our team onsite in Tucson, Arizona! To be considered for this and other roles, please create a profile at .OverviewOur site partner is seeking a dedicated and research-oriented Physician &ndash; Psychiatrist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.Key Responsibilities<ul><li>Serve as Principal Investigator or Sub-Investigator on multiple Phase I&ndash;IV clinical trials.</li><li>Perform comprehensive physical exams and clinical assessments for protocol screening and enrolment.</li><li>Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.</li><li>Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.</li><li>Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.</li><li>Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.</li><li>Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.</li><li>Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.</li><li>Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.</li><li>Educate and counsel patients on study procedures, informed consent, and potential side effects.</li><li>Support recruitment efforts and promote patient retention in trials.</li></ul>Qualifications<ul><li>MD or DO degree from an accredited medical school.</li><li>Valid, unrestricted medical license in the state of employment.</li><li>Board Certified or Board Eligible (BC/BE) in Psychiatry.</li><li>BC/BE in Family Medicine or Geriatric Medicine will also be considered.</li><li>Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.</li><li>Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.</li><li>Preferred Skills</li><li>Familiarity with FDA, ICH-GCP, and clinical trial protocols.</li><li>Experience managing or participating in industry-sponsored clinical trials.</li><li>Strong attention to detail and ability to document accurately.</li><li>Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.</li><li>Ability to work collaboratively with a cross-functional team in a fast-paced research environment.</li><li>Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).</li><li>DEA license (preferred).</li></ul>Open to RelocationNoJob Roles and ResponsibilitiesClinical Research CompliancePsychiatryClinical Research &amp; Regulatory Compliance: FDA, ICH-GCP, cGMP, HIPAA, CMS Standards, Regulatory Submissions (IND), CAPA Implementation, Quality Assurance, Risk Management, Protocol &amp; SOP Compliance, Site Monitoring Support, Informed Consent, Electronic Trial Master File (VeevaVault), EDC System (REDCap)Communication and interpersonal skillsCTMS, EMR and EDC SystemsWork AuthorizationRequiredJob Types: Part-time, ContractPay: $150.00 - $250.00 per hourExperience:<ul><li>Clinical Research: 1 year (Required)</li></ul>License/Certification:<ul><li>Board Certified or Board Eligible (BC/BE) in Psychiatry (Required)</li><li>BC/BE in Family Medicine or Geriatric Medicine (Required)</li><li>Valid, unrestricted medical license in Arizona (Required)</li></ul>Location:<ul><li>Tucson, AZ 85705 (Required)</li></ul>Work Location: In person

Principal Investigator (Psychiatrist)

DescriptionUpTrials is a new platform that helps professionals like yourself get hired faster for relevant clinical research roles. We are partnered with an organization seeking a Principal Investigator (Psychiatry) to join our team onsite in Austin, Texas! To be considered for this and other roles, please create a profile atOverviewThe Principal Investigator (PI) will lead the execution of clinical trials in Psychiatry at our assigned Psychiatry research sites. The PI will oversee all aspects of clinical trial conduct in compliance with ICH/GCP guidelines and FDA regulations, ensuring the safety of participants, integrity of data collected, and compliance with study protocols. The ideal candidate is a Board-Certified Psychiatrist with significant experience as a PI in Psychiatry trials.As a PI, you will collaborate with our operational teams, clinical coordinators, and external sponsors to execute high-quality clinical trials. This position requires clinical oversight of trial protocols, patient management, and timely reporting to sponsors and regulatory agencies.Job Description:<ul><li>Provides clinical oversight for all Psychiatry trials at our Psychiatry sites.</li></ul><ul><li>Acts as the Principal Investigator for clinical trials, ensuring compliance with protocols, ethical standards, and regulatory requirements (FDA, GCP).</li></ul><ul><li>Reviews and approves study protocols, informed consent forms, and other relevant documents.</li></ul><ul><li>Works with feasibility team to determine the enrollment potential for the site according to the protocol specifications.</li></ul><ul><li>Engages and recruits eligible participants, ensuring patient safety and proper monitoring throughout the trial.</li></ul><ul><li>Reviews patient medical history and performs assessments necessary for inclusion in clinical trials. &bull; Collaborates with site staff, clinical research coordinators, and monitors to ensure timely and accurate data collection.</li></ul><ul><li>Interfaces with sponsors, CROs, and our operations team to ensure alignment on</li></ul>study objectives and timelines.Required Skills/Abilities:<ul><li>Board certification in Psychiatry.</li></ul><ul><li>Active Medical License in assigned state with no open or past action items.</li></ul><ul><li>5+ years of experience as a Principal Investigator in clinical trials, with at least 3 years in Psychiatry trials.</li></ul><ul><li>Deep knowledge of clinical research processes, FDA regulations, ICH/GCP guidelines, and relevant ethical standards.</li></ul><ul><li>Proven ability to engage with patients and clinical staff to maintain a high standard of</li></ul>care in a research setting.<ul><li>Strong organizational skills with a demonstrated ability to manage multiple projects simultaneously.</li></ul><ul><li>Excellent written and oral communication skills for reporting and interaction with</li></ul>sponsors and clinical staff.<ul><li>Experience in patient recruitment and retention in clinical trials.</li></ul><ul><li>Familiarity with electronic data capture systems and clinical trial management software.</li></ul><ul><li>Ability to work in a fast paced environment and collaborate with site staff.</li></ul>Education and Experience:<ul><li>M.D. or D.O. degree with board certification in Psychiatry.</li></ul><ul><li>Extensive clinical and research experience in Psychiatry.</li></ul><ul><li>Prior experience as a PI in Psychiatry clinical trials.</li></ul>Open to RelocationYesJob SenioritySeniorJob Roles and ResponsibilitiesPrincipal InvestigatorClinical Operations LeadershipProgram &amp; Project ManagementTherapeutic AreasPsychiatryWork AuthorizationRequiredJob Types: Part-time, ContractWork Location: In person

Principal Investigator - GastroenterologistOct 22, 2025Huntington Beach, California, 92647, USAIn Person, Contract, Part Time$150 - $250Salary/HourlyMinimum years of clinical research experience (required)1DescriptionUpTrials is a new platform that helps professionals like yourself get hired faster for relevant clinical research roles. We are partnered with an organization seeking a Principal Investigator (Gastroenterologist) to join our team onsite in Huntington Beach, California! To be considered for this and other roles, please create a profile at .OverviewOur site partner is seeking a dedicated and research-oriented Physician &ndash; Gastroenterologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.Key Responsibilities<ul><li>Serve as Principal Investigator or Sub-Investigator on multiple Phase I&ndash;IV clinical trials.</li><li>Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.</li><li>Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.</li><li>Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.</li><li>Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.</li><li>Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.</li><li>Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.</li><li>Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.</li><li>Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.</li><li>Educate and counsel patients on study procedures, informed consent, and potential side effects.</li><li>Support recruitment efforts and promote patient retention in trials.</li></ul>Qualifications<ul><li>MD or DO degree from an accredited medical school.</li><li>Valid, unrestricted medical license in the state of employment.</li><li>Board Certified or Board Eligible (BC/BE) in Gastroenterology</li><li>BC/BE in Family Medicine or Geriatric Medicine will also be considered.</li><li>Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.</li><li>Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.</li><li>Preferred Skills</li><li>Familiarity with FDA, ICH-GCP, and clinical trial protocols.</li><li>Experience managing or participating in industry-sponsored clinical trials.</li><li>Strong attention to detail and ability to document accurately.</li><li>Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.</li><li>Ability to work collaboratively with a cross-functional team in a fast-paced research environment.</li><li>Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).</li><li>DEA license (preferred).</li></ul>Open to RelocationNoJob Roles and ResponsibilitiesClinical ResearchGastroenterologyCTMS, EMR and EDC SystemsCommunication and Interpersonal SkillsWork AuthorizationRequiredJob Types: Part-time, ContractPay: $150.00 - $250.00 per hourExperience:<ul><li>Clinical research: 1 year (Required)</li></ul>License/Certification:<ul><li>MD or DO degree from an accredited medical school (Required)</li><li>Valid, unrestricted medical license in California (Required)</li><li>Board Certified or Board Eligible (BC/BE) Gastroenterology (Required)</li><li>BC/BE in Family Medicine or Geriatric Medicine (Required)</li></ul>Location:<ul><li>Huntington Beach, CA 92615 (Required)</li></ul>Work Location: In person

Principal Investigator (Gastroenterologist)

Principal Investigator - PulmonologistSan Jose, California, USAIn Person, Part Time, Contract$150 - $250Salary/HourlyMinimum years of clinical research experience (required)1DescriptionUpTrials is a new platform that helps professionals like yourself get hired faster for relevant clinical research roles. We are partnered with an organization seeking a Principal Investigator (Pulmonologist) to join our team onsite in San Jose, California! To be considered for this and other roles, please create a profile at .OverviewOur site partner is seeking a dedicated and research-oriented Physician &ndash; Pulmonologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.Key Responsibilities<ul><li>Serve as Principal Investigator or Sub-Investigator on multiple Phase I&ndash;IV clinical trials.</li><li>Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.</li><li>Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.</li><li>Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.</li><li>Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.</li><li>Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.</li><li>Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.</li><li>Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.</li><li>Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.</li><li>Educate and counsel patients on study procedures, informed consent, and potential side effects.</li><li>Support recruitment efforts and promote patient retention in trials.</li></ul>Qualifications<ul><li>MD or DO degree from an accredited medical school.</li><li>Valid, unrestricted medical license in the state of employment.</li><li>Board Certified or Board Eligible (BC/BE) in Pulmonology.</li><li>BC/BE in Family Medicine or Geriatric Medicine will also be considered.</li><li>Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.</li><li>Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.</li><li>Preferred Skills</li><li>Familiarity with FDA, ICH-GCP, and clinical trial protocols.</li><li>Experience managing or participating in industry-sponsored clinical trials.</li><li>Strong attention to detail and ability to document accurately.</li><li>Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.</li><li>Ability to work collaboratively with a cross-functional team in a fast-paced research environment.</li><li>Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).</li><li>DEA license (preferred).</li></ul>Open to RelocationNoJob Roles and ResponsibilitiesClinical ResearchPulmonary &amp; Respiratory CarePulmonary diseasesCTMS, EMR and EDC SystemsCommunication and interpersonal skillsWork AuthorizationRequiredJob Type: ContractPay: $150.00 - $250.00 per hourExperience:<ul><li>Clinical Research : 1 year (Required)</li></ul>License/Certification:<ul><li>MD or DO degree from an accredited medical school (Required)</li><li>Valid, unrestricted medical license in California (Required)</li><li>Board Certified or Board Eligible (BC/BE) in Pulmonology (Required)</li><li>BC/BE in Family Medicine or Geriatric Medicine (Required)</li></ul>Location:<ul><li>San Jose, CA 95110 (Required)</li></ul>Work Location: In person

Principal Investigator ( Pulmonologist)

Join UpTrials and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

UpTrials

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Principal Investigator (Psychiatrist)

Principal Investigator (Psychiatrist)

Principal Investigator (Gastroenterologist)

Principal Investigator ( Pulmonologist)