Clinical Research Screener in Brussels

Beschrijving

Will you be our new ambassador?

Jefferson Wells Life Sciences specializes in supporting pharma & biotech companies in their daily challenges. Hence our interest in experts like you to pass our team. 

Let's look together at your first challenge with us!

Clinical Research screener (CRS)

Our partners innovate to bring treatments to their patients that significantly improve their lives. Together with the government and other health partners they are working towards qualitative, affordable and accessible healthcare.

The Clinical Research Screener (CRS) is responsible for registering new and current volunteers and conducting a series of screening procedures to determine eligibility for clinical studies. Screening procedures includes conducting medical phone screening reviewing health related documents, performing check on data accuracy, maintaining source documentation, data and sample collection (blood sample, ECG, blood pressure, ….), safety of trial subject …

What are your responsibilities?

• Maintain first contact with potential volunteers and informs them about clinical research (procedure, payment, and company policies) in a prompt and professional manner.
• Performs screen phones following medical and other guidance, data and sample collection and safety of trial subjects.
• Ensures the follow up and update of the volunteer files and medical reports.
• Provides appropriate medical information to ineligible volunteers.
• Assesses volunteers’ qualifications for participation in a study based on information gathered during the phone screen and accurately entering the information into the database.
• Places outgoing calls to volunteers already listed in the database research unit for appointment.
• Identify potential volunteers for a study and send them the appropriate documents.
• Work with the recruiters and patient recruiter helping them to identify, explore and implement new methods for subject recruitment to extend the panel.
• Regularly review the database in order to have an accurate information.
• Helping recruiters to identify, explore and implement new methods for subject recruitment to extend the panel.
• Maintain source documentation, accuracy, accessibility, and confidentiality of volunteer records and reports
• Handle text messaging, mailings or other communication methods towards subject’s incompliance of regulatory requirements.
• Demonstrate ability and flexibility to work evening and week-end.

Other:

• Assist in the conduct of clinical trials in the PCRU.
• Collaborate closely with team to execute projects according protocol requirements.
• May obtain signed informed consent from candidate trial-subjects.
• Participate in PCRU teams to accomplish business needs and resolve issues.
• Ensure data collection of high quality and transfer to relevant departments (medication administration and other clinical exams, ….).
• Ability to take over and manage specific projects.
• May participate in the communication and study related meetings.
• Contribute to ensure clinical trials are conducted in accordance with scientific, medical, and ethical principles, within regulatory requirements/guidelines, and Pfizer SOPs.
• May participate in other administrative parts related to the execution of Phase I clinical studies.
• Support ongoing capture and analysis of metrics to demonstrate value and increase productivity.
• Participate in the creation and implementation of global and local SOPs.

At a senior level experience:

• Oversees on-the-job-training for new colleagues in liaise with Technical Training Manager and Team Leaders.
• Contributes to the completion of project, work group or department tasks as development and training of new procedures, internal guidance, …
• May initiate new processes and procedures to improve performance and increase efficiency.
• Lead and manage daily clinical activities. Resolves potential problems.
• Assists Team members in establishing their priorities in day-to-day activities

Who are you?

• Bachelor degree in Life Science or nursing
• Language skills: good written and verbal skills in Dutch and French with good comprehension of English
• IT-minded, stress resistant, paramedical/medical background is a plus
• Flexible to work in shift (7:30 - 15:48 / 9:00 - 17:18 / 10:15-18:33)
• Knowledge of MS Office tools (Word, Excel, PowerPoint, …)
• Must be proactive, showing initiative and positive team spirit
• High sense of service and professionalism over the phone

Extra informatie

Status

Inactief

Opleidingsniveaus

Master

Plaats

Brussels

Werkuren per week

8 - 40

Dienstverbanden

Tijdelijke fulltime baan

Beroepsgroepen subcategorie

Onderwijs en Wetenschap

Rijbewijs nodig?

Nee

Auto nodig?

Nee

Motivatiebrief verplicht?

Nee

Talen

Nederlands