Clinical Study Team Associate II – FSP

Job not on LinkedIn

🔥 13 minutes ago

🌐 Brazil, Argentina, +1 more countries – Remote

🇧🇷 Brazil – Remote 🇦🇷 Argentina – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 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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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Provide study-level operational support from study start-up through close-out and submission • Maintain and oversee study team shared spaces, Trial Master Files, Study Team on Demand, client registries, and required systems • Analyze, interpret, and follow up on study metrics • Track and oversee study information and follow up with functional lines • Coordinate study-level forms and data entry into clinical operations applications and systems • Provide study-level reporting supporting clinical trial data, budgets, and timelines • Perform quality control of essential clinical trial documentation, including Clinical Study Report components and regulatory submissions • Support Independent Oversight Committees, audit and inspection readiness, and clinical trial budget tracking • Provide logistical and operational support for Investigator Meetings • Coordinate document translations as required • Provide task status updates and contribute to study team meetings • Support system setup and maintenance and global study team communications to sites • Coordinate and prioritize multiple study tasks with minimal oversight • Partner with Clinical Study Team Leads, Global Study Managers, and Study Managers on operational leadership, site management, monitoring, and vendor oversight • Support onboarding training, train and mentor new hires and entry-level CSTAs, and serve as a subject matter expert on CSTA processes, systems, and tasks • Identify continuous improvement opportunities and comply with required training, timesheets, expense reports, and CV updates

🎯 Requirements

• Bachelor’s of Art or Bachelor’s of Science with minimum of 3 years experience, or Master’s of Art, Master’s of Business Administration or Master’s of Science with minimum of 1 year experience • Proficient in Microsoft Office applications (Outlook, Word, PowerPoint, Excel, Teams) • Effective verbal and written communication skills • Fluency in written and spoken English required • Ability to work independently and as part of a larger team • Ability to multitask and manage multiple competing priorities • Self-motivated and able to organize tasks to meet timelines and deliver high-quality work • Attention to detail and disciplined approach to document review, SOP adherence, and metrics • Good problem-solving and decision-making skills • Relevant clinical research or clinical trial experience or relevant coursework in drug development or clinical research preferred • Science background preferred • Experience with clinical trial processes and applicable systems preferred • Knowledge of the drug development process preferred

🏖️ Benefits

• No benefits, perks, or compensation extras are specified in the posting