
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.
🔥 0 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Serve 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 the drug development process • Work from a home office base while supporting studies within Poland or the assigned region • Travel as required for clinical research activities
• 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, interpersonal, and problem-solving skills • 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
• 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 • Opportunity to develop within the role, take on more responsibility, or develop skill sets within other related Parexel FSP departments
Apply Now🔥 11 hours ago
Senior Clinical Research Associate monitoring oncology clinical trials for Precision for Medicine in Poland. Ensuring protocol compliance, coordinating study setup, and supporting project teams.
🗣️🇵🇱 Polish Required
🔥 11 hours ago
Senior Clinical Research Associate monitoring oncology clinical trials for Precision for Medicine, a precision medicine CRO. Managing investigative sites, regulatory activities, client interaction, and trial oversight.
🗣️🇵🇱 Polish Required
🕒 Yesterday
Clinical Study Manager supporting ICON’s sponsor-dedicated pharmaceutical programs. Coordinating global clinical trials, vendors, compliance, milestones, budgets, and inspection readiness.
🕒 October 14
Senior Clinical Research Associate monitoring oncology clinical trials remotely in Poland for Alira Health. Ensuring GCP compliance, site quality, reporting, and CRA oversight.
🇵🇱 Poland – Remote
💵 €60k - €70k / year
💰 $58M Venture Round on 2023-01
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🗣️🇵🇱 Polish Required
🕒 October 9
Senior FSA leader directing feasibility, site activation, and study start-up teams at ICON, a global healthcare intelligence and clinical research organisation. Home or office based across seven European countries.