Tucson Arizona 85704 USA
In Person Part Time Contract
$150 - $250
Salary/Hourly
Minimum years of clinical research experience (required) - 1
Description
UpTrials 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 .
Overview
Our site partner is seeking a dedicated and research-oriented Physician 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
- Serve as Principal Investigator or Sub-Investigator on multiple Phase IIV clinical trials.
- Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
- Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
- Provide medical oversight for clinical trial participants including safety assessments adverse event evaluations and ongoing care.
- Collaborate closely with Clinical Research Coordinators Sponsors and Monitors to ensure protocol compliance and data integrity.
- Review and sign off on source documents case report forms (CRFs) and regulatory documentation.
- Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP
- FDA and sponsor requirements.
- Participate in Site Initiation Visits (SIVs) Monitoring Visits and Audits as needed.
- Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
- Educate and counsel patients on study procedures informed consent and potential side effects.
- Support recruitment efforts and promote patient retention in trials.
Qualifications
- MD or DO degree from an accredited medical school.
- Valid unrestricted medical license in the state of employment.
- Board Certified or Board Eligible (BC/BE) in Psychiatry.
- BC/BE in Family Medicine or Geriatric Medicine will also be considered.
- Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
- Minimum of 1 year of experience in clinical practice; prior clinical research experience
- preferred but not required.
Preferred Skills
- Familiarity with FDA ICH-GCP and clinical trial protocols.
- Experience managing or participating in industry-sponsored clinical trials.
- Strong attention to detail and ability to document accurately.
- Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
- Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
- Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
- DEA license (preferred).
Open to Relocation
No
Job Roles and Responsibilities
Clinical Research Compliance
Psychiatry
Clinical Research & Regulatory Compliance: FDA ICH-GCP cGMP HIPAA CMS Standards Regulatory Submissions
(IND) CAPA Implementation Quality Assurance Risk Management Protocol & SOP Compliance Site Monitoring
Support Informed Consent Electronic Trial Master File (VeevaVault) EDC System (REDCap)
Communication and interpersonal skills
CTMS EMR and EDC Systems
Work Authorization
Required
Tucson 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 relevantclinical research roles. We are partnered with an organiza...
Tucson Arizona 85704 USA
In Person Part Time Contract
$150 - $250
Salary/Hourly
Minimum years of clinical research experience (required) - 1
Description
UpTrials 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 .
Overview
Our site partner is seeking a dedicated and research-oriented Physician 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
- Serve as Principal Investigator or Sub-Investigator on multiple Phase IIV clinical trials.
- Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
- Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
- Provide medical oversight for clinical trial participants including safety assessments adverse event evaluations and ongoing care.
- Collaborate closely with Clinical Research Coordinators Sponsors and Monitors to ensure protocol compliance and data integrity.
- Review and sign off on source documents case report forms (CRFs) and regulatory documentation.
- Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP
- FDA and sponsor requirements.
- Participate in Site Initiation Visits (SIVs) Monitoring Visits and Audits as needed.
- Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
- Educate and counsel patients on study procedures informed consent and potential side effects.
- Support recruitment efforts and promote patient retention in trials.
Qualifications
- MD or DO degree from an accredited medical school.
- Valid unrestricted medical license in the state of employment.
- Board Certified or Board Eligible (BC/BE) in Psychiatry.
- BC/BE in Family Medicine or Geriatric Medicine will also be considered.
- Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
- Minimum of 1 year of experience in clinical practice; prior clinical research experience
- preferred but not required.
Preferred Skills
- Familiarity with FDA ICH-GCP and clinical trial protocols.
- Experience managing or participating in industry-sponsored clinical trials.
- Strong attention to detail and ability to document accurately.
- Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
- Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
- Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
- DEA license (preferred).
Open to Relocation
No
Job Roles and Responsibilities
Clinical Research Compliance
Psychiatry
Clinical Research & Regulatory Compliance: FDA ICH-GCP cGMP HIPAA CMS Standards Regulatory Submissions
(IND) CAPA Implementation Quality Assurance Risk Management Protocol & SOP Compliance Site Monitoring
Support Informed Consent Electronic Trial Master File (VeevaVault) EDC System (REDCap)
Communication and interpersonal skills
CTMS EMR and EDC Systems
Work Authorization
Required
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