Clinical Research Associate Sponsor-dedicated at IQVIA

Athens, Greece

IQVIA Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, HealthcareIndustries

Requirements

  • High School Diploma or equivalent; Degree in a scientific discipline or healthcare preferred
  • At least 1 year of on-site monitoring experience
  • Good knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Understanding of therapeutic and protocol knowledge as provided in company training
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Experience using a laptop computer, iPhone, and iPad (where applicable)
  • Excellent written and verbal communication skills in Greek and English
  • Strong organizational and problem-solving skills
  • Effective time and financial management skills

Responsibilities

  • Conduct site monitoring visits (selection, initiation, monitoring, and close-out) according to contracted scope of work and regulatory requirements
  • Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability
  • Administer protocol and related study training to assigned sites and maintain regular communication
  • Evaluate study site practices and ensure proper conduct of the protocol, escalating quality issues as needed
  • Manage the progress of studies by tracking regulatory submissions and approvals, recruitment, CRF completion, and data query resolution
  • Create and maintain site management documentation, including visit reports, follow-up letters, and study documentation
  • Collaborate with study team members for project execution support
  • Support the development of project subject recruitment plans on a per-site basis
  • Manage site financial management according to the clinical trial agreement and retrieve invoices according to local requirements

Skills

GCP
ICH
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Site Monitoring
Subject Recruitment
Protocol Training
Regulatory Submissions
CRF Completion
Data Query Resolution
Greek
English

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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