Home › Companies › Psicro › Clinical Research Associate II
Clinical Research Associate II
Psicro · Remote, US, United States · Remote · Active · SmartRecruiters
Job facts
| Field | Value |
|---|---|
| Company | Psicro |
| Title | Clinical Research Associate II |
| Normalized title | - |
| Department / team | Clinical |
| Location | US, United States |
| Work model | Remote / Remote |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | SmartRecruiters |
| Posted / first seen | 2026-05-29 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Psicro. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through SmartRecruiters. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Department jobs | Active postings in Clinical. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Psicro |
| Source | 2a57b066-6d90-4457-bc69-3b485bbafd80 |
| ATS provider | SmartRecruiters |
Description
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.
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
Act as the main line of communication between the project team, sponsor, and the site Build and maintain a good relationship with the site staff involved in the study conduct Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level Ensures quality (data integrity and compliance) at site level Conduct site audit preparation visits and resolve site audit findings Participate in study site audits and client onsite visits, as required Ensure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse Conduct project-specific training of site investigators Support preparation of Investigator newsletters Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level Support preparation of draft regulatory and ethics committee submission packages Support collection of IP-RED packages at site/country level Facilitate review and reconciliation of the study TMF on country and site levels
College/University degree in Life Sciences or an equivalent combination of education, training & experience Located in the Central or West Coast regions is preferred Must have 2+ years of independent on-site monitoring experience Experience in all types of monitoring visits, in phases I-III Experience in Oncology mandatory & GI preferred and/or radio-pharm experience preferred. Full working proficiency in English Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel up to 75% Valid driver’s license (if applicable)
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
Full job record
| Job ID | 552a0c8c8ff4897ca3e19a6eb6055474656cdbb0 |
| Org ID | 09ee3685-cc0c-4268-bc4c-753b2a72bac7 |
| Source ID | 2a57b066-6d90-4457-bc69-3b485bbafd80 |
| Board ID | 2a57b066-6d90-4457-bc69-3b485bbafd80 |
| Provider | smartrecruiters |
| Provider Job Key | 744000129237699 |
| Title | Clinical Research Associate II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Remote, US, United States |
| Department | Clinical |
| Team | — |
| Employment Type | full_time |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | United States |
| Region | US |
| City | — |
| Salary Raw | 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. As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will: Act as the main line of communication between the project team, sponsor, and the site Build and maintain a good relationship with the site staff involved in the study conduct Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level Ensures quality (data integrity and compliance) at site level Conduct site audit preparation visits and resolve site audit findings Participate in study site audits and client onsite visits, as required Ensure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse Conduct project-specific training of site investigators Support preparation of Investigator newsletters Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level Support preparation of draft regulatory and ethics committee submission packages Support collection of IP-RED packages at site/country level Facilitate review and reconciliation of the study TMF on country and site levels College/University degree in Life Sciences or an equivalent combination of education, training & experience Located in the Central or West Coast regions is preferred Must have 2+ years of independent on-site monitoring experience Experience in all types of monitoring visits, in phases I-III Experience in Oncology mandatory & GI preferred and/or radio-pharm experience preferred. Full working proficiency in English Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel up to 75% Valid driver’s license (if applicable) This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii |
| Apply URL | https://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii?oga=true |
| First Seen At | 2026-05-31 17:36:56Z |
| Last Seen At | 2026-06-06 19:44:14Z |
| Last Checked At | 2026-06-06 19:44:14Z |
| Last Changed At | 2026-05-31 17:36:56Z |
| Inactive At | — |
| Source Posted At | 2026-05-29 18:19:45Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=psicro/date=2026-06-06/2026-06-06T19-44-10-643Z-5b05a0ec068b568c8e600a1146df1f50ddc8569c8f796facd7bdce3d9e509929.json |
Event Fields
{
"content_hash": "7ae8c948d8f878de5bbec33d4febb6f986dfe17f8ec34960d10ff60c6aef0620",
"source_hash": "d4ff9cca2b936dac1cc4a62408c10efa83b3954870de677c412044481c88e5c6",
"last_changed_at": "2026-05-31T17:36:56.970Z",
"active_status": "active"
}Parsed Structured
{
"language": "en",
"location": {
"raw": "Remote, US, United States",
"city": null,
"region": "US",
"country": "United States",
"is_remote": true,
"confidence": 0.8
},
"salary_max": null,
"salary_min": null,
"inferred_at": "2026-06-06T19:44:14.180Z",
"launch_scope": {
"reason": "english_us_canada",
"included": true,
"language": "en",
"location": {
"raw": "Remote, US, United States",
"city": null,
"region": "US",
"country": "United States",
"is_remote": true,
"confidence": 0.8
},
"countries": [
"United States"
]
},
"remote_policy": "remote",
"salary_period": null,
"workplace_type": "remote",
"salary_currency": null
}Extensions
{}Native Structured
{
"id": "744000129237699",
"ref": "https://api.smartrecruiters.com/v1/companies/psicro/postings/744000129237699",
"name": "Clinical Research Associate II",
"uuid": "15cbdd3f-199a-4ec8-a807-c10eb3b99fc2",
"detail": {
"id": "744000129237699",
"name": "Clinical Research Associate II",
"uuid": "15cbdd3f-199a-4ec8-a807-c10eb3b99fc2",
"jobAd": {
"sections": {
"videos": {
"urls": [
"https://www.youtube.com/watch?v=BZEQBN4wZGQ"
],
"title": "Videos To Watch"
},
"jobDescription": {
"text": "<p>As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.</p><p>You will:</p><ul><li>Act as the main line of communication between the project team, sponsor, and the site</li><li>Build and maintain a good relationship with the site staff involved in the study conduct</li><li>Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits</li><li>Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level</li><li>Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations</li><li>Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level</li><li>Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites</li><li>Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level</li><li>Ensures quality (data integrity and compliance) at site level</li><li>Conduct site audit preparation visits and resolve site audit findings</li><li>Participate in study site audits and client onsite visits, as required</li><li>Ensure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse</li><li>Conduct project-specific training of site investigators</li><li>Support preparation of Investigator newsletters</li><li>Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level</li><li>Support preparation of draft regulatory and ethics committee submission packages</li><li>Support collection of IP-RED packages at site/country level</li><li>Facilitate review and reconciliation of the study TMF on country and site levels </li></ul>",
"title": "Job Description"
},
"qualifications": {
"text": "<ul><li>College/University degree in Life Sciences or an equivalent combination of education, training & experience</li><li>Located in the Central or West Coast regions is preferred</li><li>Must have 2+ years of independent on-site monitoring experience</li><li>Experience in all types of monitoring visits, in phases I-III</li><li>Experience in Oncology mandatory & GI preferred and/or radio-pharm experience preferred.</li><li>Full working proficiency in English</li><li>Proficiency in MS Office applications</li><li>Ability to plan, multitask and work in a dynamic team environment</li><li>Communication, collaboration, and problem-solving skills</li><li>Ability to travel up to 75%</li><li>Valid driver’s license (if applicable)</li></ul><p> </p>",
"title": "Qualifications"
},
"companyDescription": {
"text": "<p>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.</p>",
"title": "Company Description"
},
"additionalInformation": {
"text": "<p>This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.</p><p>For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.</p>",
"title": "Additional Information"
}
}
},
"jobId": "b5e18712-a064-4068-b0b3-14b69244fe24",
"active": true,
"company": {
"name": "PSI CRO",
"identifier": "PSICRO"
},
"creator": {
"name": "Lauren Pettrey",
"avatarUrl": "https://c.smartrecruiters.com/sr-employee-image-prod-aws-dc5/6149d4e560c60977dc080677?r=s3-eu-central-1&_1636747975368"
},
"jobAdId": "703199d7-2dfa-448c-b4f1-15b0e2ef3cf4",
"applyUrl": "https://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii?oga=true",
"function": {
"id": "research",
"label": "Research"
},
"industry": {
"id": "pharmaceuticals",
"label": "Pharmaceuticals"
},
"language": {
"code": "en",
"label": "English",
"labelNative": "English (US)"
},
"location": {
"city": "Remote",
"hybrid": false,
"region": "US",
"remote": true,
"country": "us",
"fullLocation": "Remote, US, United States"
},
"refNumber": "REF3531R",
"department": {
"id": 1063561,
"label": "Clinical"
},
"postingUrl": "https://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii",
"visibility": "PUBLIC",
"customField": [
{
"fieldId": "COUNTRY",
"valueId": "us",
"fieldLabel": "Country/Region",
"valueLabel": "United States"
},
{
"fieldId": "5b615e106d8bc52f977e9866",
"fieldLabel": "Job Summary",
"valueLabel": "Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & site information."
},
{
"fieldId": "5a8ea76ab60a5e06821bfc7b",
"valueId": "default",
"fieldLabel": "Brands",
"valueLabel": "PSI CRO"
},
{
"fieldId": "5a8ea76ab60a5e06821bfc7c",
"valueId": "1063561",
"fieldLabel": "Department",
"valueLabel": "Clinical"
}
],
"referralUrl": "https://jobs.smartrecruiters.com/external-referrals/company/PSICRO/publication/15cbdd3f-199a-4ec8-a807-c10eb3b99fc2?dcr_ci=PSICRO",
"defaultJobAd": true,
"releasedDate": "2026-05-29T18:19:45.983Z",
"experienceLevel": {
"id": "associate",
"label": "Associate"
},
"typeOfEmployment": {
"id": "permanent",
"label": "Full-time"
}
},
"company": {
"name": "PSI CRO",
"identifier": "PSICRO"
},
"creator": {
"name": "Lauren Pettrey"
},
"jobAdId": "703199d7-2dfa-448c-b4f1-15b0e2ef3cf4",
"function": {
"id": "research",
"label": "Research"
},
"industry": {
"id": "pharmaceuticals",
"label": "Pharmaceuticals"
},
"language": {
"code": "en",
"label": "English",
"labelNative": "English (US)"
},
"location": {
"city": "Remote",
"hybrid": false,
"region": "US",
"remote": true,
"country": "us",
"fullLocation": "Remote, US, United States"
},
"refNumber": "REF3531R",
"department": {
"id": "1063561",
"label": "Clinical"
},
"visibility": "PUBLIC",
"customField": [
{
"fieldId": "COUNTRY",
"valueId": "us",
"fieldLabel": "Country/Region",
"valueLabel": "United States"
},
{
"fieldId": "5a8ea76ab60a5e06821bfc7b",
"valueId": "default",
"fieldLabel": "Brands",
"valueLabel": "PSI CRO"
},
{
"fieldId": "5a8ea76ab60a5e06821bfc7c",
"valueId": "1063561",
"fieldLabel": "Department",
"valueLabel": "Clinical"
},
{
"fieldId": "5b615e106d8bc52f977e9866",
"fieldLabel": "Job Summary",
"valueLabel": "Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & site information."
}
],
"defaultJobAd": true,
"releasedDate": "2026-05-29T18:19:45.983Z",
"detail_errors": [],
"experienceLevel": {
"id": "associate",
"label": "Associate"
},
"typeOfEmployment": {
"id": "permanent",
"label": "Full-time"
}
}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/552a0c8c8ff4897ca3e19a6eb6055474656cdbb0?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/09ee3685-cc0c-4268-bc4c-753b2a72bac7JSONGET https://api.bluedoor.sh/job-postings/v1/sources/2a57b066-6d90-4457-bc69-3b485bbafd80JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/552a0c8c8ff4897ca3e19a6eb6055474656cdbb0/eventsJSON