Global Study Associate – FSP

Job not on LinkedIn

🔥 16 minutes ago

🌐 Spain, Germany, +3 more countries – Remote

🇪🇸 Spain – Remote 🇩🇪 Germany – Remote 🇮🇹 Italy – Remote 🇵🇱 Poland – Remote 🇬🇧 United Kingdom – Remote

💵 €42k - €45k / year

⏰ Full Time

🟡 Mid-level

✨ Associate

👻 Ghost score 0%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Just posted.
• Jobs at this company usually fill in 21 days.

Apply Now

Find Similar Remote Jobs

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

• Support Phase 1, 2, 3, and 4 clinical studies with guidance • Support study and site feasibility, start-up, maintenance, and close-out activities • Manage study and site essential document review, collection, and tracking • Support preparation and maintenance of study documents and manuals • Provide oversight of the Trial Master File (TMF) • Ensure study documents are received, reviewed, and filed in accordance with SOPs, GCP, and applicable regulations • Organize study-related meetings, prepare agendas, take minutes, and maintain risk, issue, and decision logs • Lead and present at study-related meetings as required • Perform applicable site monitoring and co-monitoring visits • Address internal and site quality assurance findings from audits • Manage, coordinate, and oversee third-party vendor activities • Perform study tracking and maintenance, including study status, enrollment, site queries, deviations, and study-level documents and plans • Participate in clinical trial team meetings and collaborative efforts such as protocol development and CRO selection • Support study site oversight, including site performance, metrics, and monitoring report review • Support study data activities, including data review, query creation and resolution, deviation reviews, and safety reviews • Work cross-functionally and provide oversight of CRO and vendor activities • Review and verify contracted vendor activities, including vendor invoice review • Support study reporting and tracking using applicable systems and technology • Support study leads in cross-functional alignment of study timelines • Complete required training, timesheets, expense reports, and CV updates • Maintain knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements

🎯 Requirements

• A BA or BS degree, a nursing degree, or an equivalent qualification • At least 3 years of experience in clinical studies as a SCRA or Lead CRA • Working knowledge of Good Clinical Practice (GCP) regulations and Standard Operating Procedures • Understanding of study phases and how they apply to clinical development • Working knowledge of electronic systems, including the Trial Master File and CTMS (e.g., Veeva Vault, Smartsheet, SharePoint) • Knowledge of the principles and practices of computer applications in database management • 10% to 20% travel may be required • Strong verbal and written communication skills • Ability to work independently and as part of a team • Advanced knowledge of Microsoft Word, Excel, and PowerPoint • Ability to prioritize and manage multiple tasks simultaneously

🏖️ Benefits

• Premium salary • Attractive benefits • Medical care plan: Health, Dental & Vision • Life Assurance • Excellent work environment • Culture of teamwork and collaboration • People who motivate and face challenges together • Innovative technology • Excellent training • Paid time off • Life insurance • Health insurance • Additional benefit offerings in accordance with the terms of applicable plans • Additional incentives, bonuses, or other compensation programs may be available for eligible roles

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume