11 days ago on hays.ch

Global Studies Associate II (m/f)

Hays (Schweiz) AG

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Global Studies Associate II (m/f)

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We are looking for a

Global Studies Associate II (m/f)

for a contracting project assignment in the Basel region
  • Reference number:
  • Start date:
  • Project duration:
    12 MM++
Your Duties:
  • You will provide operational support for multiple global Study Management Teams (SMTs)
  • You will develop and maintain effective working relationships with members of the SMT involved in running clinical studies such as Global Studies Managers (GSMs), Global Studies Leaders (GSLs), affiliate team members, Clinical Research Organization (CRO) partners and vendors
  • You will assist the GSM with effective communication and information sharing within the SMT and with external partners
  • You will be responsible for reviewing and maintaining accurate study level progress information through the efficient use of systems, tools and reports
  • You will review standard study related reports and liaise with accountable study members to address any inconsistencies and missing information, as appropriate
  • You will identify any data or quality issues through the use of study related reports and ensure any discrepancies are escalated through the correct pathway
  • You will provide the SMT with guidance and know-how to support the effective use of system functionality and reports to ensure consistency across SMTs
  • You will coordinate activities with CRO vendors to meet study timelines
  • You will be responsible for communication between the study team and vendor for defined tasks and tracking information
  • You will troubleshoot issues ensuring vendor and CROs are meeting study timelines and escalate to the study team as appropriate
  • You will be responsible for managing the delivery of non-drug equipment to sites
  • You will promote standardisation and foster improvements in efficiency in Study Management practices and processes ensuring consistent delivery across studies
Your Qualifications:
  • Bachelor's degree with experience in a clinical research or health care related industry, or equivalent combination of education and experience, life sciences degree or nursing equivalent is preferred
  • Knowledge of ICH/GCP
  • Familiarity/experience with clinical trials and the pharmaceutical industry
  • Experience in working as part of a large team with a proven ability to make an active contribution to the team's performance
  • Good written and verbal communication skills
  • Proficient computer skills across multiple applications
Hier bewerben
Hier bewerben
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