CRA II / Senior CRA – Sponsor-Dedicated

🕒 August 21, 2025

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Conduct on-site and remote monitoring of clinical research studies • Verify the accuracy and completeness of collected data and adherence to study protocols • Develop and implement quality-monitoring tools, procedures, processes, standardized templates, and site-visit checklists • Contribute to clinical trial processes, programs, policies, protocols, study design, and methodology • Manage and direct lower-level professionals or clinical trial processes and programs • Provide guidance and support to junior staff and oversee day-to-day clinical trial site activities • Ensure accurate and timely clinical trial documentation and reporting • Maintain detailed site-visit and monitoring records and prepare reports for regulatory submissions • Collaborate with data management, biostatistics, and regulatory affairs teams • Identify and resolve clinical trial conduct and data-integrity issues • Train and mentor junior staff on monitoring techniques and best practices

🎯 Requirements

• Bachelor's degree in a related field • Minimum of 3-5 years of experience in clinical research or a related field • In-depth knowledge of clinical trial processes and regulations • Strong analytical and problem-solving skills • Excellent communication and interpersonal skills • Ability to work independently and as part of a team • Proficiency in clinical trial management systems and software • Strong organizational and time management skills • Attention to detail and accuracy • Ability to manage multiple projects and priorities simultaneously • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements • Certified Clinical Research Professional (CCRP) or equivalent certification preferred

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture supporting authenticity and inclusion • Diversity, equity, and belonging-focused workplace culture

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