Working at CT-N

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Freelance Senior Clinical Research Associate

Overview

ClinTrial-Net (CT-N) is a young clinical contract research organization (CRO), based in Belgium. We provide Phase I-IV clinical development support services to the life sciences industry (biotechnology, pharmaceutical- and medical devices). Our mission is to accelerate the clinical development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Job Description

As our clinical activities are growing, we are looking for a 0.5-0.8 FTE freelance Senior CRA, experience in oncology is an asset, 80% home-based to join us. As a freelance Senior CRA, you will be responsible for the monitoring of clinical trials and tracking of study progress. You will contribute to the overall management of clinical trials in accordance with the appropriate quality standards including ICH-GCP guidelines, Standard Operating Procedures (SOPs), applicable regulations, rules and guidance. You will be responsible for clinical site start-up, maintenance, and closure activities, including maintenance of study documents.
Responsibilities

* Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
* Perform source document verification and eCRF review; regulatory document(s) collection and quality check review of essential documents (including PIS/ICF) ; conduct study drug inventory; adverse event and serious adverse event reporting and assess patient recruitment and retention.
* Assists with the ongoing management of the Trial Master File (TMF) and/or Investigator Site Files (ensuring essential documents are filed appropriately) and the maintenance / update of project-related data in an existing database, e.g. CTMS.
Qualifications

* Bachelor or Master of Science in a health-related / scientific field;
* 2-8 years of previous experience as a CRA and in Oncology;
* Fluent in the local languages (Dutch and French) and very good in English;
* Proven IT proficiency and skills including Microsoft Office.
* Effective time management and organizational skills

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Parttime Study Nurse

Overview

Are you looking for variety in your daily work or for something additional? If you find clinical research appealing, then we have a great opportunity for you.
As a young and dynamic company that supports doctors/hospitals in carrying out clinical studies, we are looking for a part-time study nurse.
Job Description
- During consultations, you support the attending physician.
- You collect the necessary data according to the clinical study protocol.
- You do the follow-up of the study patients and consult with the treating physician.
- For practical and administrative questions about the study you are the central contact.
- Attending necessary training(s) for this position.
Profile
- You have a bachelor's degree in Nursing or equivalent.
- Minimum 1 year experience in clinical studies is important.
- Experience in oncology is a plus.
- Socially competent, highly communicative, with the necessary persuasion, in dealing with patients.
- Discreet and professional.
- Autonomous and precise working.
- Good basic knowledge of the English language is a must.
- Fluent in PC (Word, Excel).
- Freelancers are welcome.
Offer
- Salary based on hours worked.
- Mileage allowance
- Daily allowance
- Expense allowance
- Or on a freelance basis