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HomeCompaniesPsicroClinical Research Associate II

Clinical Research Associate II

Psicro · Remote, US, United States · Remote · Active · SmartRecruiters

Job facts

FieldValue
CompanyPsicro
TitleClinical Research Associate II
Normalized title-
Department / teamClinical
LocationUS, United States
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusactive
ATS providerSmartRecruiters
Posted / first seen2026-05-29 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Psicro.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Department jobsActive postings in Clinical.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyPsicro
Source2a57b066-6d90-4457-bc69-3b485bbafd80
ATS providerSmartRecruiters

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 ID552a0c8c8ff4897ca3e19a6eb6055474656cdbb0
Org ID09ee3685-cc0c-4268-bc4c-753b2a72bac7
Source ID2a57b066-6d90-4457-bc69-3b485bbafd80
Board ID2a57b066-6d90-4457-bc69-3b485bbafd80
Providersmartrecruiters
Provider Job Key744000129237699
TitleClinical Research Associate II
Normalized Title
Statusactive
Activeyes
Location TextRemote, US, United States
DepartmentClinical
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
RegionUS
City
Salary RawPSI 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 URLhttps://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii
Apply URLhttps://jobs.smartrecruiters.com/PSICRO/744000129237699-clinical-research-associate-ii?oga=true
First Seen At2026-05-31 17:36:56Z
Last Seen At2026-06-06 19:44:14Z
Last Checked At2026-06-06 19:44:14Z
Last Changed At2026-05-31 17:36:56Z
Inactive At
Source Posted At2026-05-29 18:19:45Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=psicro/date=2026-06-06/2026-06-06T19-44-10-643Z-5b05a0ec068b568c8e600a1146df1f50ddc8569c8f796facd7bdce3d9e509929.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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