Archer Research | Clinical Research Associate (CRA)

Jobbeschrijving

Archer is a young, dynamic and growing Contract Research Organization (CRO) based in Bioville, Diepenbeek. We are specialized in providing full support for clinical studies with medical devices in Europe.

As a CRA you manage and conduct clinical studies by respecting all regulatory requirements and Good Clinical Practice (GCP). You are the primary contact for investigational staff and responsible to ensure the quality and integrity of the clinical data. You will monitor multiple projects within different therapeutic areas, and you must be able to work both independently and in a team environment.

Who are we looking for?

• You have a profound curiosity for clinical research & medical innovations.
• You are familiar with guidelines like Good Clinical Practice (GCP) and ISO standards (ISO14155, ISO9001).
• The EU Regulations for medical devices (MDR) and General Data Protection Regulation (GDPR)
  do not sound unknown to you.
• You have a Master’s degree or Ph.D. degree in one of the Life Sciences.
• You love to travel and build strong relationships with site staff, representatives and sponsors.
• You have excellent written and verbal communication skills including good command of English. Knowledge of German and/or French is definitely a plus.
• People describe you as being confident, flexible, pro-active and result-driven, with attention to
  detail and accuracy in work.
• You excel in effective time management and organization, with the ability to manage multiple priorities across various clinical studies within various disciplines and a problem-solving mentality.
• Computer skills, including working knowledge of Microsoft Word, Excel, PowerPoint and Electronic Data Capture (EDC) systems are checked in your competences list.

What is your role?

• Preparation and follow-up of ethical committee and/or national competent authority
  submissions in European member states.
• Select potential investigators by verifying the investigators’ interest, qualifications, training and
  resources, including investigational site facilities, equipment, and staff
• Conduct pre-study visits, site initiation and study close-out visits to ensure data integrity and
  patient safety on site.
• Conduct clinical study monitoring (remote and on-site) to ensure adherence to the study
  protocol, Good Clinical Practice (GCP) in accordance with International Conference on
  Harmonization (ICH)-GCP standards, Declaration of Helsinki and Regulatory Requirements in
  order to guarantee data integrity, good documentation practice and patient safety.
• Support and advice investigators and site staff about study-related matters.
• Provide training to site staff as well as sponsor representatives about study-related matters.
• Coordinate planning and execution of investigator meetings.
• Assess and follow-up on patient recruitment and retention.
• Set-up and manage safety board and/ or Imaging Core Lab.
• Ensure correct and timely Adverse Event (AE) and Serious Adverse Event (SAE) reporting and
  follow-up.
• Perform reconciliation of the Trial Master File (TMF) content to Investigator Site Files (ISF).
• Develop and manage (study-specific) clinical study documentation, including tools and
  templates.
• Keep track of the study budget.
• Creating, implementing and adhering to standard operating procedures (SOPs) for study
  execution.

Interested to join the Archer Research team? Do not hesitate to send your CV to info@archerresearch.eu.

Aanbod