Single Sponsor Senior CRA - Oncology (UK based) Must have UK on-site and risk based monitoring exp)

Single Sponsor Senior CRA – Oncology (UK based)

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Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work, so we are easier to work with and easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.

Job Responsibilities

• Conduct on‑site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including verifying the accuracy and completeness of data collected and ensuring adherence to study protocols.
• Develop and implement tools, procedures, and processes to ensure quality monitoring, including creating standardized templates for monitoring reports and checklists for site visits.
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of clinical trial protocols and providing input on study design and methodology.
• Manage and direct the work of lower‑level professionals or manage processes and programs, providing guidance and support to junior staff members and overseeing the day‑to‑day activities of clinical trial sites.
• Ensure accurate and timely documentation and reporting of clinical trial data, maintaining detailed records of site visits and monitoring activities and preparing comprehensive reports for regulatory submissions.
• Collaborate with cross‑functional teams to support clinical trial activities, working closely with data management, biostatistics, and regulatory affairs teams to ensure successful execution of clinical trials.
• Identify and resolve issues related to clinical trial conduct and data integrity, troubleshooting problems with data collection and addressing discrepancies in study records.
• Provide training and mentorship to junior staff members, conducting training sessions on monitoring techniques and best practices and offering ongoing support and guidance to help them develop their skills and expertise.

Qualifications

• 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.

Certifications

• Certified Clinical Research Professional (CCRP) or equivalent certification preferred.

Necessary Skills

• 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.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all novel FDA‑approved drugs, 95% of EMA‑authorized products, and over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever‑changing environment. Learn more about Syneos Health: Syneos Health.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Roles within the Clinical Monitoring/CRA job family at the P23 level are responsible for monitoring clinical research studies to ensure that trials are conducted in accordance with widely accepted clinical practices. This includes conducting on‑site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, who may manage two or fewer employees and direct the work of lower‑level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies.

Core Focus

• Ensure regulatory, ICH‑GCP, and protocol compliance during site qualification, site initiation, interim monitoring, site management, and close‑out visits.
• Evaluate overall performance of site and site staff, provide recommendations regarding site‑specific actions, and communicate serious issues to the project team.
• Verify the process of obtaining informed consent, protect the confidentiality of subjects/patients, and assess factors affecting subject/patient safety and clinical data integrity.
• Conduct Source Document Review, verify clinical data accuracy and completeness, and apply query resolution techniques.
• Verify site compliance with electronic data capture requirements and investigational product (IP) inventory, reconciliation, storage, and security.
• Review Investigator Site File (ISF) for accuracy, timeliness, and completeness, and reconcile contents with the Trial Master File (TMF).
• Document activities via confirmation letters, follow‑up letters, trip reports, communication logs, and other required project documents.
• Manage site‑level activities and communication to ensure project objectives, deliverables, and timelines are met.
• Act as primary liaison with study site personnel, ensure training and compliance with applicable requirements, and provide guidance towards audit readiness standards.
• Provide direct supervision, training, and mentorship to junior level CRAs.