Clinical Research Associate II

🕒 June 9

🏄 California – Remote

🏄 California – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 41%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• 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

🎯 Requirements

• 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)

🏖️ Benefits

• This is a great opportunity for you to further develop your skills • Widen your therapeutic area experience • Become an expert in clinical research