Lead Clinical Research Associate

🕒 August 4

🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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

• Oversee and guide the clinical team while driving trial activities at country or regional level • Monitor project timelines, patient enrollment, data cleaning, compliance, and corrective and preventive measures • Review monitoring visit reports and ensure regional reporting compliance • Coordinate communication among Monitors, Site Management Associates, Regional Project Leads, and Project Managers • Lead country-level project team calls and provide status updates and reports • Provide project-specific training and prepare training materials • Supervise source data verification, data-query follow-up, and site-level study-risk management • Ensure proper handling, accountability, reconciliation, and return of investigational products and clinical study supplies • Review essential study documents and supervise ISF/TMF reconciliation • Ensure site-level data integrity and compliance • Collaborate on investigator/site feasibility, site identification, and study startup • Manage query resolution, including Central Monitoring observations • Coordinate safety-information flow and protocol/process-deviation reporting • Manage clinical supplies with vendors at country and regional levels • Keep study-specific and corporate tracking systems updated • Coordinate supervised monitoring visits and conduct visits • Manage site contracting and payments • Conduct audit preparation visits, participate in site audits, and coordinate resolution of findings • Oversee CAPA development and implementation • Coordinate process-deviation review, management, and reporting • Conduct initial training and authorization monitoring visits for Monitors • Mentor newly promoted Lead CRAs • Deliver training and presentations at Investigator Meetings • Ensure subject-recruitment targets and project timelines are defined, communicated, recorded, and met • Ensure timely information flow with trial sites regarding Adverse Events and protocol/process deviations • Supervise Site Management Associates handling documents and laboratory supplies • Support preparation of regulatory and ethics committee submission packages

🎯 Requirements

• Relevant educational background such as MD, MPharm, RN, or a college/university degree in Life Sciences, or equivalent combination of education, training, and experience • Minimum 4 years of site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent qualification level • Experience monitoring sites in the US • Experience with all types of monitoring visits in Phase II and/or III • Strong experience in Oncology preferred • Experience in Radiation Therapy, Radiopharmaceuticals, CAR-T Therapy, other Cell Therapy, Gene Therapy, or Nuclear Medicine preferred • Strong experience in GI (Crohn's, Ulcerative Colitis, IBS) preferred • Full working proficiency in English • Proficiency in MS Office applications • Ability to plan, multitask, and work in a dynamic team environment • Excellent communication, collaboration, and problem-solving skills • Ability to travel • Must not require a work visa for employment or continued employment now or in the future

🏖️ Benefits

• Remote work • Low-travel model • Confidential handling of applicant information according to EEO guidelines