채용
Benefits & Perks
•Company car or car allowance
•Flexible Hours
•Remote Work
•Flexible Hours
•Remote Work
Required Skills
GCP
Site monitoring
Protocol training
Clinical CRA – FSP Model
About IQVIA
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
About the Clinical FSP Business
IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises 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. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.
Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are 'indication and molecule experts'. Additionally, IQVIA's FSP business works with the Sponsors SOP's, creating more continuity for both parties.
Our models offer excellent opportunities for experienced CRA's to expand their knowledge and skills.
Role Details
- Working in partnership with a single-sponsor
- Usually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
- Responsible for approximately 10 sites
- On site between 6 and 9 days per month, dependant on the sponsor
- All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
- Permanent employment contract
- Fantastic work/life balance
- Sponsor model has reduced travel (approx. 30% or less) due to using 'Fit for Purpose Monitoring' which incorporates remote monitoring therefore there is less need for on-site visits
Responsibilities
- Site management and monitoring activities across the country
- 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
Qualifications
To become part of our team, you should:
- Have a degree in Life Sciences or have equivalent experience within a nursing background
- Have at least 12 months 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 and clean driving license
- Possess strong communication, written and presentation skills (must have fluency in English and Dutch language)
What We Offer
- Excellent salary and benefits package
- Company car or car allowance
- Flexible working hours in a home-based role
- Stable workload with investment in keeping our teams stable
- Genuine career development opportunities for those who want to grow as part of the organisation
- Opportunity to work on cutting edge medicines, right at the forefront of new medicine development
Why Join Us
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
With the merger between Quintiles and IMS Health, we now have access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. It's the next generation of clinical development.
Whatever your career goals, we are here to ensure you get there!
Forge a career with greater purpose, make an impact, and never stop learning.
Learn more at https://jobs.iqvia.com
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About IQVIA

IQVIA
PublicFocused on health information technology and clinical research.
10,001+
Employees
Durham
Headquarters
$17B
Valuation
Reviews
3.9
2 reviews
Work Life Balance
2.5
Compensation
2.0
Culture
2.8
Career
3.0
Management
2.5
65%
Recommend to a Friend
Pros
Structured feedback and development process
Meaningful contribution to client businesses
Problem-solving with specialized knowledge
Cons
Strict performance requirements and termination risk
High-level rubric definitions lack detail
No performance bonuses offered
Salary Ranges
42 data points
Junior/L3
Senior/L5
Junior/L3 · Analyst
2 reports
$107,910
total / year
Base
$93,834
Stock
-
Bonus
-
$97,750
$118,068
Interview Experience
3 interviews
Difficulty
3.0
/ 5
Duration
14-28 weeks
Experience
Positive 0%
Neutral 33%
Negative 67%
Interview Process
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
Common Questions
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
News & Buzz
IQVIA Holdings Collaboration With Boehringer Ingelheim Supports Undervalued Thesis - simplywall.st
Source: simplywall.st
News
·
5w ago
Ritter Daniher Financial Advisory LLC DE Acquires Shares of 4,267 IQVIA Holdings Inc. $IQV - MarketBeat
Source: MarketBeat
News
·
5w ago
IQVIA and Boehringer Ingelheim collaborate on therapeutic data transformation - Pharmaceutical Business review -
Source: Pharmaceutical Business review -
News
·
5w ago
IQVIA to Share its DaaS+ Platform in Boehringer Ingelheim Collaboration - Contract Pharma
Source: Contract Pharma
News
·
5w ago