Back to job search

Clinical Research Associate

  • Location:

    Brussels, Belgium

  • Contact:

    Charlotte Evens

  • Job type:

    Contract

  • Contact phone:

    +32 15 28 40 43

  • Industry:

    Life Sciences, Clinical Research

  • Contact email:

    charlotte_evens@oxfordcorp.com

Are you a Clinical Research Associate or Clinical Trial Associate with a good knowledge of Dutch, French and English ? You have a mature attitude, are a real teamplayer and can also work well independently ? Then you just may be the candidate our client is looking for to strengthen their team of Clinical Research Associates.

Job Description

As Clinical Research Associate, you will plan, execute and support clinical site management activities. The Clinical Research Associate needs to ensure the quality and integrity of the data collected in our client's sponsored clinical trials.

Responsibilities

  • The Clinical Research Associate evaluates, initiates, monitors & closes out clinical trial sites.
  • The Clinical Research Associate ensures appropriate site compliance and data quality
  • The Clinical Research Associate responds to site-related queries and escalates site-related issues
  • The Clinical Research Associate is responsible for operational site management
  • The Clinical Research Associate will actively contribute to results oriented department goals
  • As Clinical Research Associate, you will drive continuous improvement of Global Country Study Management (GCSM)
  • The Clinical Research Associate promotes operational and scientific excellence within local GCSM
  • The Clinical Research Associate identifies opportunities and best practices with local and regional partners that will contribute to overall operational effectiveness
  • The Clinical Research Associate develops site visit plans, conducts Clinical Site Evaluation, Initiation, Monitoring and Close Out visits and prepares reports from these visits for local project manager approval.
  • As Clinical Research Associate, you will build and maintain solid and long-term professional relationships with investigators and site staff
  • The Clinical Research Associate will facilitate subject enrolment at the site level with focused patient recruitment strategies and action plans
  • The Clinical Research Associate needs to implement new technologies and systems at clinical sites, e.g. EDC systems
  • The Clinical Research Associate will assist in preparing sites for audits, review audit reports and contribute to resolving findings
  • As Clinical Research Associate, you will identify site needs and site-related issues, escalate and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process
  • The Clinical Research Associate ensures appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAES)
  • The Clinical Research Associate has to verify case reports and source documentation
  • As Clinical Research Associate you will be responsible for the input and maintain electronic site management systems
  • The Clinical Research Associate provides input into Clinical Monitoring Plans as requested
  • The Clinical Research Associate has to provide input into case report forms and study-related documents as requested
  • The Clinical Research Associate needs to perform investigational product accountability and reconciliation.
  • As Clinical Research Associate you will maintain site study supplies
  • As Clinical Research Associate, you will facilitate the resolution of clinical queries to investigative staff
  • As Clinical Research Associate, you have to provide input into feasibility and identify clinical investigators

Requirements

  • You hold a Bachelor or Master degree in lifesciences (Biomedical sciences, Pharmaceutical Sciences, Rehabilitation Sciences, or any other scientific field)
  • Preferably, you already have work experience as Clinical Research Associate, or in life sciences or a medically related field, including biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical settings
  • ICH/ GCP Guidelines plus local codes of practice as applicable are familiar to you
  • You put attention to detail
  • You hold strong organizational skills
  • You are a good networker in building relationships and influencing other parties
  • You have good skills in time management & prioritization
  • You have a flexible mindset
  • You have good written and oral communication skills in Dutch, French and English
  • Good working knowledge of common software packages (e.g. M.S.)
  • You have strong presentation skills
  • You have no issues with solving problems
  • You love to work in team as well as individually
  • Existing right to work in Europe required

Benefits

  • You will receive a contract of unlimited duration
  • A very balanced salary package (including a company car, fuel card, 12 additional holidays, insurances, ...)
  • You will be able to have a very nice work-life balance

Vacancy number: 18352