Site relationship management role ensuring sustainable trial start - up for assigned sites in clinical drug development at Novartis. Collaborating with global teams and ensuring adherence to clinical operations standards and timelines.
About the role
- Clinical Research Associate managing site activities across multiple protocols for a single sponsor. Engaging in monitoring, training, and recruitment efforts for clinical studies.
Responsibilities
- Manage site activities and monitoring across France
- Collaborate with sites to develop, drive and track subject recruitment plans
- Deliver protocol and study training to assigned sites
- Create and maintain monitoring visit reports and action plans
- Where appropriate, co-monitor, train and mentor junior team members
Requirements
- Degree in Life Sciences or equivalent nursing experience
- Minimum 2 years of independent on-site monitoring experience
- Experience managing multiple protocols across various drug indications with strong time-management skills
- In-depth knowledge of GCP
- Flexible and able to travel nationwide
- Hold a full, clean French driving license
- Strong verbal, written and presentation skills; fluency in English and French required
Benefits
- Competitive salary and benefits package
- Flexible working hours with office-based or home-based options
- Professional development opportunities
- Opportunity to work on cutting-edge medicines
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
Clinical Research Associate 2 at Emerald Clinical overseeing clinical trials and conducting site management activities. Ensuring compliance with regulatory requirements and quality standards in clinical research.
Research Associate contributing to NIH - funded studies in Dr. Christina Dyar's lab. Managing operations and participant communications, while contributing to manuscripts and presentations.
Medical Research Associate conducting clinical assessments and phlebotomy at ICON. Responsible for ensuring volunteer health and comfort during trials in a research environment.
Experienced Clinical Research Associate working with sponsor dedicated team. Conducting site selection, monitoring, and collaboration with clinical experts to ensure regulatory compliance.
Clinical Research Associate overseeing oncology studies and ensuring compliance in clinical trials at IQVIA. Engaging with sites, managing progress, and training investigative resources.
Equity Research Associate conducting extensive company and industry research to develop investment recommendations. Collaborating with senior analysts and attending industry conferences at Piper Sandler.
Equity Derivatives Research Analyst conducting research on crypto derivatives. Responsible for generating trade strategies and engaging with industry partners at Delta Exchange.
Senior Research Analyst advising energy companies on supply chain and market volatility. Delivering insights through SaaS platforms and collaborating with cross - functional teams in oil & gas.
Senior Clinical Research Associate managing clinical trial sites for Parexel. Ensuring compliance, training site staff, and maintaining study integrity throughout the process.