Experienced Clinical Research Associate, Sponsor Dedicated
il y a 4 semaines
IQVIA Clinical Functional Services Partnerships (FSP) business is unique in its approach to quality delivery for customers. Our teams are dedicated to a single sponsor partner, where collaboration and face-to-face contact are key to success. We set ourselves apart with our ability to adapt and evolve, ensuring that our clinical teams are equipped to handle the latest challenges in the industry.
Leadership recognizes the skills, talent, and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors' priorities and the individual aspects of each model, providing a supportive environment for career development.
Our FSP model offers excellent opportunities for experienced CRAs to expand their knowledge and skills. We invest in keeping our teams stable, so workload is consistent, and we offer genuine career development opportunities for those who want to grow as part of the organisation.
What We Offer:
- Excellent salary and benefits package
- Flexible working hours in an office-based or a home-based role
- We invest in keeping our teams stable, so workload is consistent
- We offer genuine career development opportunities for those who want to grow as part of the organisation
- We give the chance to work on cutting-edge medicines, right at the forefront of new medicine development
Role Details:
- Working in partnership with a single sponsor
- Usually allocated to 2-3 protocols (likely to be in the areas of Oncology, Neurology, Immunology, and/or Diabetes)
- Responsible for approximately 15 sites
- On-site between 6 and 9 days per month, dependent on the sponsor
- All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
- Permanent employment contract
- Sponsor model has reduced travel (approx. 30% or less) due to using 'the Risk-Based monitoring which incorporates remote monitoring therefore there is less need for on-site visits
Responsibilities:
- Site management and monitoring activities across France
- Work with sites to adapt, drive, and track subject recruitment plan
- Provide protocol and study training to the assigned sites
- Create and maintain monitoring visit reports and action plans
- If appropriate, co-monitor, train, and mentor junior members of the team
Requirements:
- Have a degree in Life Sciences or have equivalent experience within a nursing background
- Have at least 2 years of independent on-site monitoring experience
- Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
- Have in-depth GCP knowledge
- Be flexible with the ability to travel nationwide
- Hold a full French and clean driving license
- Possess strong communication, written, and presentation skills are a must (must have fluency in English and French language)
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