Sr CRA in Oncology - Sponsor dedicated - Home Based France

Sr CRA in Oncology - Sponsor dedicated - Home Based France

Updated: October 28, 2025Location: FRA-RemoteJob ID:

Description

Sr CRA in Oncology - Sponsor dedicated - Home Based France

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 continuously look for ways to simplify and streamline our work, making Syneos Health easier to work with and easier to work for.

Collaborate with passionate problem solvers and innovate as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies.

Discover what our 29,000 employees, across 110 countries, already know:

• We are passionate about developing our people through career development, supportive line management, technical and therapeutic area training, peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself.
• We continuously build the company we all want to work for and our customers want to work with, fostering a sense of belonging.

Job Responsibilities

• Conduct on‑site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, case report forms, and regulatory documents.
• Develop tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and standard operating procedures.
• Contribute to the design, implementation, and delivery of processes, programs, and policies by providing expert input and feedback during development and review stages.
• Direct the work of lower‑level professionals or manage processes and programs, including training and mentoring junior staff and overseeing their monitoring activities.
• Ensure trials are conducted in accordance with regulatory requirements and company standards by performing regular audits and inspections, and addressing any compliance issues that arise.
• Provide guidance and support to clinical research teams, including answering questions, resolving issues, and facilitating communication between team members and stakeholders.
• Maintain accurate and timely documentation of monitoring activities, including writing detailed monitoring reports, tracking study progress, and updating databases.
• Identify and resolve issues related to clinical trial conduct, such as protocol deviations, data discrepancies, and adverse events, and implement corrective and preventive actions as needed.
• Collaborate with cross‑functional teams to ensure successful trial execution, including working with project managers, data managers, biostatisticians, and regulatory affairs specialists.

Qualifications

• Bachelor's degree in a related field.
• Minimum of 5 years of experience in clinical research monitoring; this role is a progression from Sr CRA I.
• 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 Associate (CCRA) or equivalent certification preferred.

Necessary Skills

• Proficiency in clinical trial management systems and software.
• Ability to manage multiple projects and priorities.
• Strong attention to detail and organizational skills.
• Ability to travel as required for on‑site monitoring.
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

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.

Further, nothing contained herein should be construed to create an employment contract... The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate.

Contact

Phone: Fax: Toll‑Free:

Equal Opportunity Statement

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: