Experienced Clinical Research Associate, Multi-Sponsor, Belgium

IQVIA LLC; Brussel Hoofdstad; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Attractive benefits package

Flexible work schedules

Resources for career growth

Résumé du poste

IQVIA LLC is seeking an Experienced Clinical Research Associate for their Site Management team in Brussels, Belgium. This role offers the opportunity to gain experience in various therapeutic areas while managing site operations for clinical studies.

The ideal candidate will have over 2 years of experience as a CRA, possess excellent communication skills in Dutch, French, and English, and a relevant university degree. Benefits include career growth resources and flexible work schedules.

Qualifications

• Minimum 2 years of experience as a Clinical Research Associate (CRA).
• Excellent command of Dutch, French, and English.
• Driver's license class B.

Responsabilités

• Perform site monitoring visits in accordance with GCP and ICH guidelines.
• Work with sites to track subject recruitment plans.
• Evaluate the quality and integrity of study site practices.
• Manage the progress of assigned studies and regulatory submissions.
• Create and maintain documentation for site management.

Connaissances

Clinical Research Monitoring

Site Management

Communication Skills

Organizational Skills

Problem-Solving Skills

Time Management

Computer Skills (MS Office)

Formation

University degree in scientific discipline or healthcare

Description du poste

## Experienced Clinical Research Associate, Multi-Sponsor, BelgiumApplylocations: Brussels, Brussels-Capital Region, Belgiumtime type: Full timeposted on: Posted Todayjob requisition id: R1552876***Clinical Research Associate***IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.**Your responsibilities will include:*** Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines* Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.* Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.* Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate.* If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.* If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.**Your Profile*** University degree in scientific discipline or health care* 2+ years of experience as a CRA* Very good computer skills including MS Office* Excellent command of Dutch, French and English language. Belgium based.* Organizational, time management and problem-solving skills* Ability to establish and maintain effective working relationships with coworkers, managers, and clients* Flexibility to travel* Driver’s license class B**What you can expect:*** Resources that promote your career growth* Leaders that support flexible work schedules* Programs to help you build your therapeutic knowledge* Excellent working environment in a stabile, international, reputable company* Company car, mobile phone and attractive benefits packagingIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.