PSI CRO Jobs Hiring Now
PSI CRO is hiring for 14 open roles on Migrate Mate as of July 16, 2026, concentrated in clinical trials & medical research and account management. Migrate Mate updates PSI CRO's live openings daily. PSI CRO is a contract research organization providing clinical development services to biotechnology and pharmaceutical companies across global drug development programs.
Find PSI CRO JobsOverview
PSI CRO hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 14
- Top team
- Clinical Trials & Medical Research
- Seniority
- Manager level or above
- Work type
- 64% remote or hybrid
- Top location
- Remote
Open Roles at PSI CRO
Showing 14 of 14+ PSI CRO jobs
PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.
Home-Based in United States
Responsibilities:
- Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions
- Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions
- Monitors trial participant safety
- Participates in trial participant recruitment boost and retention activities
- Presents on medical matters at kick-off and investigator meetings
- Trains trial team in the therapeutic area and medical aspects of the protocol
- Develops and reviews trial-specific documents within the scope of medical monitoring
- Manages ongoing trial risks related to medical monitoring
- Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial
- Reviews protocol deviations
- Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues
- Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request)
- Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s)
- Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases
- Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs)
- Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable
- Prepares for and participates in trial audits, follows up on audit findings
- Participates in feasibility assessment of potential and ongoing trials in the country/region
- Participates in bid defense meetings and other interactions with clients
- Acts as a medical expert and provides therapeutic expertise to other PSI departments
Qualifications
- Medical Doctor degree required
- US Board Certification in psychiatry required
- Experience as a practicing psychiatrist (minimum of 10 years)
- Clinical Research experience preferred
- Proficiency with MS Office applications
- Communication, presentation and analytical skills
- Problem-solving, team and detail-oriented
Additional Information
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.
PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.
Home-Based in United States
Responsibilities:
- Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions
- Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions
- Monitors trial participant safety
- Participates in trial participant recruitment boost and retention activities
- Presents on medical matters at kick-off and investigator meetings
- Trains trial team in the therapeutic area and medical aspects of the protocol
- Develops and reviews trial-specific documents within the scope of medical monitoring
- Manages ongoing trial risks related to medical monitoring
- Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial
- Reviews protocol deviations
- Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues
- Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request)
- Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s)
- Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases
- Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs)
- Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable
- Prepares for and participates in trial audits, follows up on audit findings
- Participates in feasibility assessment of potential and ongoing trials in the country/region
- Participates in bid defense meetings and other interactions with clients
- Acts as a medical expert and provides therapeutic expertise to other PSI departments
Qualifications
- Medical Doctor degree required
- US Board Certification in psychiatry required
- Experience as a practicing psychiatrist (minimum of 10 years)
- Clinical Research experience preferred
- Proficiency with MS Office applications
- Communication, presentation and analytical skills
- Problem-solving, team and detail-oriented
Additional Information
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.
Job Roles at PSI CRO
Working at PSI CRO
PSI CRO's 14 open roles are manager level or above, and about 64% are remote or hybrid. The most active teams are clinical trials & medical research, account management, and business operations. PSI CRO is a contract research organization that supports clinical trials and drug development for biotechnology and pharmaceutical clients, with roles spanning clinical operations, biostatistics, medical monitoring, project management, and site technology. Most PSI CRO roles are based in Remote, with some in Durham and Tulsa.
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Browse jobs by rolePSI CRO Jobs: Frequently Asked Questions
How many jobs is PSI CRO hiring for right now?
PSI CRO is hiring for 14 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in clinical trials & medical research and account management. Positions span clinical operations, biostatistics, medical monitoring, and project management, with openings at multiple seniority levels across remote and office-based locations.
What kinds of roles does PSI CRO hire for?
The most active teams are clinical trials & medical research, account management, and business operations. PSI CRO's open positions include clinical study coordinators, medical monitors requiring board certification in specialties such as psychiatry and gastroenterology, principal statisticians with pharmacokinetics expertise, project managers, operations managers, and site technology specialists. Most postings are manager level or above, reflecting the technical and regulatory demands of clinical research.
Are PSI CRO jobs remote or in-person?
Mostly remote. About 64% of PSI CRO's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Remote. Each PSI CRO listing shows its work location so you can filter before applying.
How do I apply to a job at PSI CRO?
Find a PSI CRO role on Migrate Mate, then follow the listing directly to PSI CRO's own application page. PSI CRO manages its own hiring process, so you submit your application, complete any assessments, and communicate with their recruiting team through their system. Migrate Mate keeps listings current so you see only active openings.
Does PSI CRO hire entry-level?
Most of PSI CRO's open roles on Migrate Mate are manager level or above as of July 16, 2026. Entry-level openings are limited. Check individual PSI CRO listings for stated experience requirements.
Where is PSI CRO hiring?
Most PSI CRO roles are based in Remote, with some in Durham and Tulsa, and about 64% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.