Contractor CRA_Belgium

Tigermed; Belgique; Sur place; EUR 45 000 - 65 000; Plein temps

Résumé du poste

Tigermed is seeking a skilled Clinical Research Associate to lead site management activities—from site selection and initiation to ongoing monitoring—in accordance with protocol and regulatory standards.

You will train site staff on ICH-GCP, ensure timely safety reporting, manage budgets and study materials, and maintain trial master files to support high-quality clinical trials.

Qualifications

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 year of CRA experience.
• Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures.
• Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsabilités

• Site management including study site selection, initiation (SIV) and clinical monitoring.
• Perform pre-study visits to ensure eligible sites are selected per criteria.
• Prepare and conduct SIV to train site staff for study start and conduct.
• Ensure PI/study staff complies with safety reporting requirements per protocol and regulations.
• Track study recruitment to achieve targets.
• Conduct monitoring visits per SDV plan and coordinate with sites.
• Coordinate study materials and EC submissions.
• Assemble site-specific EC submission dossier and ensure submission.
• Provide ongoing training on ICH-GCP and study protocol.
• Maintain essential documents and trial master files.
• Prepare study records archiving.
• Finalize budget and obtain contracts from sites prior to initiation.
• Update and maintain Study tools and systems.

Connaissances

GCP knowledge

MS Office proficiency

CRA experience

Formation

Bachelor degree in Medical, Pharmacology or Biology

Outils

Microsoft Word

Excel

PowerPoint

Outlook

Description du poste

Responsibilities

(a) Site management

• Study site selection, initiation (SIV) and clinical monitoring.
• Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.
• Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.
• Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.
• Track study recruitment to ensure recruitment target is achieved in all studies.
• Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.
• Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.
• Assemble site specific EC submission dossier, and ensure submission to EC.

Training

• Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
• Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

• Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.
• Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

• Ensure safety information is disseminated to all sites according SOP and applicable regulations.
• Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

• Finalize budget and obtain signed contract from site, prior to site initiation visit.
• Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

• Update and maintain Study tools/systems in a timely manner.

3. Qualifications

• 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.
• 3.2 At least 8 year of CRA experience;
• 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
• 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.