Senior CRA – Oncology

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🎲 Risk

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

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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 tools, procedures, processes, standardized monitoring report templates, and site-visit checklists • Contribute to clinical trial processes, programs, policies, protocols, study design, and methodology • Manage and direct lower-level professionals, processes, and programs • Provide guidance and support to junior staff and oversee clinical trial site activities • Maintain accurate and timely clinical trial documentation and reporting • Prepare comprehensive reports for regulatory submissions • Collaborate with data management, biostatistics, regulatory affairs, and other cross-functional 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 • Certified Clinical Research Professional (CCRP) or equivalent certification preferred • 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 • Must be UK based • Must have UK on-site and risk based monitoring experience

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Remote work arrangement