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Clinical Trial Associate I
Under supervision, provides confidential and efficient clinical trial administrative support to Global Clinical Programs team. Primary responsibilities are supporting study managers in delivery of clinical trials in accordance with project timelines, regulatory standards and company SOPs. Co-coordinating effective communication between outsourcing vendors and other departments across R&D.
EDUCATION & EXPERIENCE REQUIREMENTS
• Bachelor's degree or relevant equivalent experience preferred
• Minimum 1 year's experience in CRO or Pharmaceutical industry (Some experience of clinical trials administration or clinical document management preferred.
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BioTech FYI Center