In-House Clinical Research Associate (CRA)

Reference Number: 896329-W
Type of placement: Permanent
Location: CH, NW

Introduction:

The ideal candidate should have 7 to 10 years of previous clinical related experience, attention to detail and be motivated to work in complex clinical studies with small patients’ population.

Main Responsibilities:

  • Responsible for carrying out duties related to co-monitoring and monitoring in compliance with applicable SOPs, international regulations and directions from management;
  • Conducting all clinical site monitoring activities according to the monitoring plan and in accordance with the study timelines and company objectives;
  • Facilitating Quality Assurance Audits, as instructed;
  • Providing review of monitoring reports generated by other CRAs, escalating issues;
  • Responsible for liaising with the clinical sites to provide instruction, clarification or support, as needed;
  • Responsible for managing and monitoring the logistics associated with the shipment of clinical samples from study patients;
  • Responsible for ongoing review of data entered into the eCRF system, serving as a support for the site staff;

Qualifications and Experience:

  • University degree or equivalent in health sciences, nursing or pharmacy or related field
  • Minimum of 7 years of clinical related experience in either the pharmaceutical or CRO industries;
  • Excellent command of written and verbal English;
  • Any additional languages (ie French, German, Italian or Spanish) would be advantageous;
  • Excellent organisational and time management skills;
  • Attention to detail;
  • Ability to work under pressure;
  • Pro- active, flexible and able to multi-task;
  • Self-motivated;
  • Work in a team and independently;
  • IT literacy, particularly in Word, Excel, PowerPoint and Access
  • Only applicants with relevant working/residency permit or Swiss/EU-Citizenship, will be considered.

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