Clinical Research Associate II at PSI CRO

, , United States -

Full Time

Start Date

Immediate

Expiry Date

12 Aug, 26

Salary

0.0

Posted On

14 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

On-site Monitoring, Source Data Verification, Clinical Trial Management, Oncology, Gastrointestinal Research, TMF Reconciliation, Site Audit Preparation, Regulatory Submission, MS Office, Problem Solving, Collaboration, Multitasking

Industry

Pharmaceutical Manufacturing

Description

Company 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. Job Description 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 Qualifications 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) Additional Information 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.

Responsibilities

The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while managing data integrity and compliance.