Experienced Clinical Research Associate, Sponsor-dedicated at IQVIA

Paris, Île-de-France, France

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Clinical Research, HealthcareIndustries

Requirements

Degree in Life Sciences or equivalent experience within a nursing background
At least 2 years of independent on-site monitoring experience
Experienced in handling multiple protocols across a variety of drug indications
In-depth knowledge of Good Clinical Practice (GCP)
Flexible with the ability to travel nationwide (approximately 30% or less due to risk-based monitoring)
Hold a full French and clean driving license
Strong communication, written, and presentation skills

Responsibilities

Conduct site management and monitoring activities across France
Work with sites to adapt, drive, and track subject recruitment plans
Provide protocol and study training to assigned sites
Create and maintain monitoring visit reports and action plans
Co-monitor, train, and mentor junior team members (if appropriate)
Usually allocated to 2-3 protocols, likely in Oncology, Neurology, Immunology, and/or Diabetes
Responsible for approximately 15 sites
On-site between 6 and 9 days per month, dependent on the sponsor

Skills

Key technologies and capabilities for this role

GCPOn-site MonitoringSite ManagementProtocol ManagementRisk-Based MonitoringProtocol TrainingSubject RecruitmentMonitoring ReportsOncology ProtocolsNeurology ProtocolsImmunology ProtocolsDiabetes Protocols

Questions & Answers

Common questions about this position

What is the salary for this Experienced Clinical Research Associate position?

This information is not specified in the job description.

Is this role remote or onsite, and where?

The position is onsite/remote in Bordeaux, Lille, Lyon, Nantes, or Marseille, with on-site visits between 6 and 9 days per month and travel nationwide approximately 30% or less due to risk-based monitoring.

What are the key requirements and skills for this CRA role?

Candidates need a degree in Life Sciences or nursing experience, at least 2 years of independent on-site monitoring, experience handling multiple protocols, in-depth GCP knowledge, strong communication skills, and a full French driving license.

What benefits does IQVIA offer for this position?

IQVIA provides an excellent salary and benefits package, flexible working hours, career development opportunities, and the chance to work on cutting-edge medicines.

What makes a strong candidate for this CRA role at IQVIA?

Strong candidates have at least 2 years of independent on-site monitoring experience, expertise in multiple protocols especially in Oncology, Neurology, Immunology, or Diabetes, in-depth GCP knowledge, and strong communication skills, with flexibility for travel and site management across about 15 sites.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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