採用
福利厚生
•Flexible Hours
•Remote Work
•Learning
必須スキル
Clinical monitoring
GCP
Site management
Protocol knowledge
IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.
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. 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.
What we Offer:
- Excellent salary and benefits package
- Flexible working hours in an office-based or a home-based role in Bordeaux, Lille, Lyon, Nantes, Marseille,
- 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
Become part of our team.
We believe in hiring the best talent in the industry.
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 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)
- 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!
We invite you to join IQVIA™.
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.
#CRASDAJD
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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IQVIAについて

IQVIA
PublicIQVIA Holdings, Inc. is an American company based in Durham, North Carolina, focused on health information technology and clinical research.
10,001+
従業員数
Durham
本社所在地
$17B
企業価値
レビュー
3.6
10件のレビュー
ワークライフバランス
3.8
報酬
2.5
企業文化
4.0
キャリア
3.2
経営陣
2.8
65%
友人に勧める
良い点
Good work-life balance
Supportive team and collaborative environment
Flexible hours and good benefits
改善点
Compensation below industry standards
High workload and overwhelming at times
Poor management communication and organization
給与レンジ
51件のデータ
Junior/L3
Senior/L5
Junior/L3 · Analyst
2件のレポート
$107,910
年収総額
基本給
$93,834
ストック
-
ボーナス
-
$97,750
$118,068
面接体験
3件の面接
難易度
3.0
/ 5
期間
14-28週間
体験
ポジティブ 0%
普通 33%
ネガティブ 67%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
よくある質問
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
ニュース&話題
Whittier Trust Co. Has $4.04 Million Stake in IQVIA Holdings Inc. $IQV - MarketBeat
MarketBeat
News
·
3d ago
IQVIA Holdings stock (US46266C1053): Is its data-driven healthcare edge strong enough to unlock new - AD HOC NEWS
AD HOC NEWS
News
·
3d ago
IQVIA.ai Launch With NVIDIA Puts IQVIA’s AI Valuation In Focus - Yahoo Finance
Yahoo Finance
News
·
5d ago
Is It Time To Reconsider IQVIA (IQV) After This Year’s 23.7% Share Price Decline - simplywall.st
simplywall.st
News
·
5d ago