Clinical Research Associate, Single Sponsor dedicated in Poland at IQVIA

Warsaw, Masovian Voivodeship, Poland

IQVIA Logo
Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, Life Sciences, HealthcareIndustries

Requirements

  • A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
  • Experience in on-site monitoring of clinical trials
  • Alternatively, an equivalent combination of education, training and experience
  • Written and verbal communication skills, including good command of Polish and English language

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits
  • Maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication and administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Skills

Key technologies and capabilities for this role

Clinical Trial MonitoringSite ManagementSite SelectionSite InitiationMonitoring VisitsClose-out VisitsCRF CompletionData Query ResolutionRegulatory SubmissionsPolishEnglish

Questions & Answers

Common questions about this position

Is this Clinical Research Associate position remote?

Yes, the position is remote.

What is the salary for this role?

This information is not specified in the job description.

What are the key requirements for this Clinical Research Associate position?

Candidates need a Bachelor’s degree in a health care or scientific discipline (or equivalent), experience in on-site monitoring of clinical trials, and strong written and verbal communication skills in Polish and English.

What is the company culture like at IQVIA?

IQVIA advocates for diversity and inclusion, believing it provides a competitive advantage, fosters belonging, builds stronger teams, and allows employees to maximize their potential in an inclusive and respectful workplace.

How do I apply for this Clinical Research Associate position?

Learn more and apply at https://jobs.iqvia.com.

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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