20 beste vacatures voor de functie van drug development in brussel (nieuwe medewerkers gezocht)

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Home Based role requiring local submissions experience as well as fluency within Dutch, French and English.

Essential Functions

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.
Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines.
Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience.

Ability to manage multiple projects.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.

IQVIA 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.com

IQVIA 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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Nu solliciteren

Verfijn je zoekopdracht

drug development vacatures in brussel

Study Start Up Management Specialist - Belgium

Research Associate – Cellular and Biochemical Assays (M/F)

Drug Safety Advisor

Medical Development Program - Physician (New to Industry)

Biological Project Leader in drug Substance

Oncology Emerging Therapeutics Medical Advisor

Downstream Biomanufacturing Process Expert

Study Design Lead

Pharmacovigilance Specialist - VIE Contract

Senior R & D Laboratory Coordinator | Brussels

SSO Country Manager (Satellite Country)

Nervous system rewiring upon developmental stress

Medical Device UniQuality & Unidata Product Information Specialist

Principal Statistical Methodologist (Belgium)

Principal Statistical Methodologist

H.U.B – Professeur en Immuno-oncologie – Temps plein (h/f/x)

VIE Bioanalytical Scientist

Global Head, Data Evaluation and Enablement

Solutions Quality Lead

Contract Negotiator 2 - FSP - Belgium

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van drug development in brussel

Zoek vacatures in meer locaties

Where you'll work

Home-based

Culture

Tools voor werkzoekenden

Werkgeverstools

Bladeren

Blijf verbonden