Senior Clinical Research Associate – FSP

🕒 June 9

🇵🇱 Poland – Remote

💵 zł230k - zł260k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

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

• Work as a sponsor-dedicated Senior Clinical Research Associate • Perform all site management and supervisory activities in assigned oncology studies • Conduct independent site monitoring visits • Work with industry leaders and subject matter experts • Mentor junior CRAs • Use world-class technology • Support clinical studies from a home office base within Poland • Contribute to the drug development process

🎯 Requirements

• Extensive experience in site management, with knowledge of clinical trial methodology and terminology • Minimum 5 years’ experience in independent site monitoring of all types of visits • Minimum 2 years’ experience as CRA in oncology • Effective time management, organizational and interpersonal skills • Problem-solving skills, with the ability to multitask and prioritize • Good understanding and working knowledge of clinical research • Knowledge of clinical trial phases • Current GCP/ICH knowledge • Knowledge of country clinical research legislation and guidelines

🏖️ Benefits

• Premium salary • Attractive benefits • Car or car allowance • 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 • Annual performance-based bonus plan for eligible roles • Annual salary review for eligible roles • Total rewards incentives for eligible roles • Opportunities to develop careers in the long term • Opportunities to take on more responsibility or develop skill sets within related Parexel FSP departments • Work from home • Opportunities to travel