Clinical Research Associate , Multisponsor Team at IQVIA

Bucharest, Bucharest, Romania

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Pharmaceuticals, HealthcareIndustries

Requirements

MSc and/or BSc education level, preferable in Health Sciences
Proficient level of Romanian and English
Romania based
Good knowledge and application of ICH-GCP
Minimum of 1 year of experience as a CRA
Experience in using CTMS, eTMF and EDC systems
Experience in different studies, phases, visits and therapeutic indications
Passion for science, helping patients and collaborating with the sites
Availability to travel across the country, driving license

Responsibilities

Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines
Support of the site(s) i.v.m. patient recruitment
RCA and CAPA management
Reporting of visits and progress of the studies
Management and archiving of study documents in eTMF
Collaboration with the project/study team
Documentation in Monitoring Visit Reports and follow-up letters

Skills

Key technologies and capabilities for this role

ICH-GCPCTMSeTMFEDCCRAPatient RecruitmentSite MonitoringRCACAPAMonitoring Visit Reports

Questions & Answers

Common questions about this position

What work arrangement does this position offer?

The role offers a hybrid model with both office-based and home-based options available.

What is the salary or remuneration for this CRA position?

This information is not specified in the job description.

What qualifications and experience are required for this Clinical Research Associate role?

Candidates need an MSc and/or BSc, preferable in Health Sciences, minimum 1 year of experience as a CRA, good knowledge of ICH-GCP, proficiency in Romanian and English, and experience with CTMS, eTMF, and EDC systems.

What does the company culture and work environment look like at IQVIA?

IQVIA emphasizes focus on quality over quantity, stable teams with consistent workload, passion for science and helping patients, collaboration with sites, and invests in career development.

What makes a strong candidate for this multisponsor CRA position?

Strong candidates have experience in different studies, phases, visits, and therapeutic indications, availability to travel across Romania with a driving license, and a passion for science and patient care.

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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