SCRA (Clinical Research Associate) - Major Pharma

Highly Competitive
  1. Permanent
  2. Clinical Research Associate (CRA)
  3. Belgium
Brussels, Belgium
Posting date: 19 Oct 2023

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a SCRA (Clinical Research Associate) - Major Pharma to join a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Belgium.


  • Accountable for assisting with various studies concurrently.
  • Support in preparing project specific materials such as status reports, newsletters, templates, study manuals/binders, etc.
  • Conduct quarterly QC of allocated studies/sites in the eTMF rendering to the company's oncology SOPs.
  • Keep updated on site information, this involves all contact details and distribution lists for reports and clinical supplies.
  • Work alongside other members of the project team to meet sponsor, protocol and company goals of regulatory promptness which involves contract and budget deliberations when needed.
  • Offer assistance to project management through ongoing project reports and updates.
  • Form and uphold efficient, regular communications with study sites, offering study updated and assistance to sites in a timely manner.
  • Recognise and raise data quality concerns to guarantee clinical data integrity.
  • Conduct ongoing management of necessary regulatory documentation at the outset as well as across the lifespan of a study.
  • Contribute to the performance of pre-qualification, initiation, regular monitoring, remote monitoring, and close-out visits rendering to pertinent SOPs.
  • Other duties to be assigned.

Key Skills and Requirements:

  • Educated to a degree level in a biological or human-connected field or corresponding work experience.
  • Demonstrable experience in a clinical research associate role with a background in managing clinical trial sites.
  • Familiarity with supervising oncology early phase studies.
  • Know-how of ICH regulations and GCP which involves comprehension of regulatory needs.
  • Expertise on the drug development process and the company's organisational structure.
  • Exhibits a professional attitude with good customer orientation.
  • Interpersonal and communication skills both verbally and in writing.
  • Works well both independently as well as in a team.
  • Able to multitask and manage time efficiently.
  • An organised individual with computer literacy.
  • Competent working remotely as well as absorbing and implementing expertise gained through both internal and external trainings on protocols allocated.
  • Willing to travel for business needs.
  • Fluency English as well as 2 other languages being either French, Spanish, Dutch or German.

If you are having difficulty in applying or if you have any questions, please contact Jack Wingrove at +44 203 831 7675.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.