Clinical Research Associate (Late Phase Research) at IQVIA

Seoul, South Korea, South Korea

Apply Now

Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

At least 2 years of PMS, OS, Late Phase study or relevant experience (Oncology or Global study experience preferred)
Good English communication skills

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring, and close-out) in accordance with contracted scope of work and Good Clinical Practice
Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability
Administer protocol and related study training to sites and establish regular communication to manage expectations and issues
Evaluate quality and integrity of site practices related to protocol conduct and regulatory adherence; escalate issues as appropriate
Manage study progress by tracking regulatory submissions, recruitment, enrollment, CRF completion/submission, and data query resolution; support start-up phase as needed
Ensure site documents are available for Trial Master File (TMF) and verify Investigator's Site File (ISF) maintenance per GCP and local requirements
Create and maintain documentation for site management, monitoring findings, and action plans via visit reports, follow-up letters, and other study documents
Collaborate and liaise with study team members for project execution support
If applicable, support development of project subject recruitment plans on a per-site basis
If applicable, manage site financials per clinical trial agreement and retrieve invoices per local requirements

Skills

Key technologies and capabilities for this role

Site MonitoringGood Clinical PracticeGCPSite ManagementProtocol TrainingSubject RecruitmentRegulatory SubmissionsTrial Master FileTMFInvestigator Site FileISFCRF CompletionData Query ResolutionClinical Trial Agreements

Questions & Answers

Common questions about this position

What experience is required for this Clinical Research Associate role?

At least 2 years of PMS, OS, Late Phase study or relevant experience is required, with oncology or global study experience preferred.

What is the employment type for this position?

This is a full-time position on a client dedicated team as a regular employee (정규직 포지션).

What benefits does IQVIA offer?

Benefits include internal career development opportunities, Employee Assistance Program, club activities, team workshops, celebratory packages, holiday bonuses, birthday allowances, childcare support, company iPhone, remote work activation, and flexible working hours.

What is the application process for this job?

Submit an English CV through this job posting. The process includes resume screening, online pre-screening (respond within 72 hours of email), interview (video or in-person), final selection, and onboarding; all applicants receive results notification.

What skills are essential for this role besides experience?

Good English communication skills are required.

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.

Land your dream remote job 3x faster with AI

Try Jobo Free