Parexel Senior Clinical Research Associate Recruitment 2026: Apply Online for Multiple Vacancies
Senior Clinical Research Associate – Poland – FSP
Job Overview
Parexel is seeking a highly skilled and dedicated Senior Clinical Research Associate (CRA) to join their Functional Service Provider (FSP) division in Poland. This home-based position offers an exceptional opportunity to work with a single dedicated client, focusing on cutting-edge oncology clinical trials. As a Senior CRA, you will play a pivotal role in ensuring the safety and well-being of patients while driving the drug development process forward. You will be responsible for comprehensive site management, conducting all types of monitoring visits, and maintaining the highest standards of clinical data quality.
Working within the FSP model at Parexel provides the unique advantage of combining the stability and resources of a world-class CRO with the focused exposure of working directly with industry-leading pharmaceutical and biotech sponsors. This role is designed for self-starters who possess strong organizational skills, a detail-oriented mindset, and a passion for clinical excellence. Parexel fosters a supportive, inclusive, and collaborative work environment, empowering employees to achieve their professional goals while maintaining a healthy work-life balance.
- Single Client Dedication: Focus your expertise on a single sponsor’s pipeline, allowing for deeper relationship building and protocol mastery.
- Oncology Focus: Manage complex oncology studies, contributing directly to life-saving cancer research.
- Flexible Work Environment: Enjoy the autonomy of a home-based role with manageable site-to-protocol ratios.
- Professional Development: Access structured career pathways to transition into project leadership, people management, or technical specialization.
Key Job Details
| Company Name | Parexel |
| Job Role | Senior Clinical Research Associate – Poland – FSP |
| Experience | Minimum 2 years of independent site monitoring of all types of visits, with at least 2 years specifically in oncology. |
| Salary Range | PLN 200,000 – 260,000 per annum |
| Job Category | Graduation Jobs, Private Jobs |
| Job Type | Full-Time |
| Work Mode | Home-based / Remote |
| Openings | Multiple |
| Job Location | Poland (Home-based: Trojmiasto/ Bydgoszcz/ Koszalin/ Szczecin) |
Key Responsibilities
- Dedication to a single client, managing all site activities and supervisory tasks for assigned oncology studies.
- Conducting independent site monitoring visits, including Site Initiation (SIV), Interim Monitoring (IMV), and Close-Out Visits (COV).
- Ensuring investigator sites comply with the study protocol, ICH-GCP guidelines, and local regulatory requirements.
- Performing source data verification (SDV) and ensuring the accuracy, completeness, and legibility of clinical trial data.
- Managing safety reporting, including prompt identification and documentation of Serious Adverse Events (SAEs).
- Building strong, collaborative relationships with site investigators and study coordinators.
- Mentoring and providing guidance to junior CRAs and clinical trial assistants.
- Utilizing advanced clinical trial technologies and electronic data capture (EDC) systems.
Requirements & Qualifications
- Minimum of 2 years of experience in independent site monitoring of all types of clinical trial visits.
- Minimum of 2 years of dedicated experience in independent site monitoring of oncology trials.
- Extensive knowledge of clinical trial methodology, terminology, and operational workflows.
- Strong working knowledge of ICH-GCP guidelines and local clinical research legislation in Poland.
- Excellent time management, organizational, and multi-tasking capabilities.
- Proactive problem-solving skills with the ability to resolve site-level issues independently.
- Fluency in Polish and professional proficiency in English (written and spoken).
Required Skills
- Excellent communication and interpersonal skills.
- High attention to detail and strong organizational capabilities.
- Adaptability and flexibility in a dynamic clinical trial environment.
- Proactive problem-solving and critical-thinking abilities.
- Self-motivated with a high degree of personal accountability.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) platforms.
About Parexel
Parexel is one of the world’s leading global clinical research organizations (CRO), dedicated to providing a comprehensive range of Phase I to IV clinical development services. With a patient-first philosophy, Parexel partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of innovative treatments. The company is recognized for its collaborative culture, commitment to diversity and inclusion, and robust professional development programs that empower employees to work ‘With Heart’ to improve global health outcomes.
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