CRA II in MultiSponsor - Based in Paris Office

Syneos Health, Inc.; Paris; Sur place; EUR 60 000 - 82 000; Plein temps

Résumé du poste

Syneos Health in Paris is seeking a CRA II in MultiSponsor to join the Clinical Solutions team based in Paris Office. You’ll conduct site qualification, initiation, interim monitoring, and close‑out visits on‑site or remotely, ensuring regulatory compliance and data integrity.

Strong communication, presentation and interpersonal skills are essential, along with knowledge of GCP/ICH guidelines and the ability to travel up to 75% regularly to sites across the region.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements.
• Strong computer skills and openness to new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% on a regular basis.
• US ONLY: Compliance with site access information requirements for employment; understanding that non‑compliance may result in employment risk.

Responsabilités

• Performs site qualification, initiation, interim monitoring, site management activities and close‑out visits (onsite or remotely) ensuring regulatory and protocol compliance; evaluates site performance and provides recommendations; communicates/escalates serious issues; develops action plans.
• Verifies informed consent process for each subject; protects confidentiality; assesses safety and data integrity risks such as protocol deviations and pharmacovigilance issues.
• Assesses site processes per the Clinical Monitoring/Site Management Plan; conducts source document review and verifies clinical data entry in the CRF; resolves queries remotely and on‑site; supports electronic data capture compliance.
• Manages investigational product inventory, reconciles storage and security, and ensures proper dispensing and administration; handles IP labeling and compliance with local regulations.
• Reviews the Investigator Site File for accuracy, timeliness and completeness; reconciles with the Trial Master File; ensures archiving per local guidelines.
• Documents activities through letters, reports, logs and other required project documents per SOPs and monitoring plans.
• Supports subject recruitment, retention and awareness strategies; enters data into tracking systems to monitor observations and action items.
• Manages site‑level activities, budgets and timelines; adapts to changing priorities to meet goals and targets.
• Acts as liaison with site personnel, training and ensuring compliance with applicable requirements.
• Prepares for and attends Investigator Meetings and sponsor face‑to‑face meetings; participates in global monitoring/project staff meetings and attends training sessions as required.
• Guides sites toward audit readiness and supports audit preparation and follow‑up actions.
• Maintains a working knowledge of ICH/GCP Guidelines, local regulations and company SOPs; completes required training.
• Supports site throughout the study lifecycle; performs chart abstraction; collaborates with sponsor affiliates, medical science liaisons and local staff; may train junior staff; identifies out‑of‑scope activities and recommends potential sites.

Connaissances

Excellent communication

Presentation skills

Interpersonal skills

Formation

Bachelor’s degree or RN

Outils

Computer skills

Tech-savvy

Description du poste

CRA II in MultiSponsor - Based in Paris Office

Updated: July 16, 2026
Location: Paris, 75, France
Job ID:25109492

Description

CRA II in MultiSponsor - Based in Paris Office

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum to help them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying years of experience and deep expertise to understand customer needs and represent those in the solutions we shape.

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 customers achieve their goals. We are agile and driven to deliver for one another, our customers, and most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

• We are passionate about developing our people through career development and progression, supportive line management, technical and therapeutic area training, peer recognition and a total rewards program.
• We are committed to building an inclusive culture where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures our passion to shape solutions that can dramatically impact someone’s life.
• We continuously build the company we all want to work for and the customers want to work with, knowing that when we bring together smart colleagues from across the world we can shape the future of healthcare and drive impact for customers and patients.

We partner with early stage and late stage clinical research studies, helping world‑remarkable medical innovators bring cures and treatments to the market and provide hope and health worldwide.

Job Responsibilities

• Performs site qualification, initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) ensuring regulatory and protocol compliance; evaluates site performance and provides recommendations; communicates/escalates serious issues; develops action plans.
• Verifies informed consent process for each subject; protects confidentiality; assesses safety and data integrity risks such as protocol deviations and pharmacovigilance issues.
• Assesses site processes per the Clinical Monitoring/Site Management Plan; conducts source document review and verifies clinical data entry in the CRF; resolves queries remotely and on‑site; supports electronic data capture compliance.
• Manages investigational product inventory, reconciles storage and security, and ensures proper dispensing and administration; handles IP labeling and compliance with local regulations.
• Reviews the Investigator Site File for accuracy, timeliness and completeness; reconciles with the Trial Master File; ensures archiving per local guidelines.
• Documents activities through letters, reports, logs and other required project documents per SOPs and monitoring plans.
• Supports subject recruitment, retention and awareness strategies; enters data into tracking systems to monitor observations and action items.
• Manages site‑level activities, budgets and timelines; adapts to changing priorities to meet goals and targets.
• Acts as liaison with site personnel, training and ensuring compliance with applicable requirements.
• Prepares for and attends Investigator Meetings and sponsor face‑to‑face meetings; participates in global monitoring/project staff meetings and attends training sessions as required.
• Guides sites toward audit readiness and supports audit preparation and follow‑up actions.
• Maintains a working knowledge of ICH/GCP Guidelines, local regulations and company SOPs; completes required training.
• Supports site throughout the study lifecycle; performs chart abstraction; collaborates with sponsor affiliates, medical science liaisons and local staff; may train junior staff; identifies out‑of‑scope activities and recommends potential sites.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements.
• Strong computer skills and openness to new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.
• US ONLY: Compliance with site access information requirements for employment; understanding that non‑compliance may result in employment risk.

Get to Know Syneos Health

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

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

http://www.syneoshealth.com

Additional Information

Tasks, duties and responsibilities listed in this job description are not exhaustive. The Company may assign additional tasks, duties or responsibilities. Equivalent experience, skills and/or education will also be considered, so qualifications of incumbents may differ. The Company will determine what constitutes equivalence. Nothing herein creates an employment contract. All language herein complies with legislation in each country of operation, including the EU Equality Directive. The Company is committed to compliance with the Americans with Disabilities Act, providing reasonable accommodations when appropriate.

Summary

Roles within Clinical Monitoring/CRA oversee and ensure the integrity of clinical research studies, conduct remote monitoring, identify potential issues, and collaborate with site teams to enhance quality and support successful clinical trials.