Senior Clinical Research Associate - Sponsor Dedicated at IQVIA

Amsterdam, North Holland, Netherlands

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Pharmaceutical, Clinical ResearchIndustries

Requirements

  • Have a degree in Life Sciences or equivalent experience within a nursing background
  • Have at least 3 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 and clean driving license
  • Possess strong communication, written and presentation skills (must have fluency in English and Dutch language)

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

Skills

Key technologies and capabilities for this role

Clinical ResearchCRAOncologyNeurologyImmunologySOPProtocol ManagementSite MonitoringRegulatory CompliancePatient Data Management

Questions & Answers

Common questions about this position

What compensation and benefits are offered for this role?

The position offers an excellent salary and benefits package, including a company car or car allowance.

Is this a remote or home-based position, and what's the travel requirement?

This is a home-based role with flexible working hours and reduced travel of approximately 30% or less due to 'Fit for Purpose Monitoring' incorporating remote monitoring, requiring on-site presence between 6 and 9 days per month.

What are the key qualifications and skills required for this Senior CRA role?

Candidates need a degree in Life Sciences or equivalent nursing experience, plus at least 3 years of independent on-site monitoring experience. Experience in site management, monitoring, subject recruitment, protocol training, and mentoring junior team members is essential.

What is the company culture like in IQVIA's Clinical FSP business?

The FSP model features dedicated teams for a single sponsor, emphasizing collaboration, face-to-face contact, career development from day one, stable workloads, and expertise in specific indications and molecules while following sponsor SOPs.

What makes a strong candidate for this Senior Clinical Research Associate position?

Strong candidates have a Life Sciences degree or nursing background with at least 3 years of independent on-site monitoring experience, plus skills in site management and a passion for career growth in a dedicated sponsor model.

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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