Experienced Clinical Research Associate, Sponsor Dedicated
il y a 4 semaines
At IQVIA, we're dedicated to delivering quality results for our customers. Our Clinical Functional Services Partnerships (FSP) business is unique in that our teams work closely with a single sponsor partner to achieve this goal. We prioritize collaboration and face-to-face contact to ensure seamless communication and successful study execution.
Our leadership recognizes the value of our clinical teams' skills and experience, and we strive to build on this as the function evolves. Our managers understand the sponsor's priorities and work closely with each team member to ensure their career development and growth.
One of the key benefits of our FSP model is that our CRAs become 'indication and molecule experts', contributing to the sponsor's pipeline. We also work closely with the sponsor's SOPs, creating continuity and efficiency for both parties.
Our models offer excellent opportunities for experienced CRAs to expand their knowledge and skills, and we're committed to providing a stable and consistent workload.
What We Offer:
- Excellent salary and benefits package
- Flexible working hours in an office-based or 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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