PSI CRO AG
PSI CRO AG
PSI CRO AG एक वैश्विक कॉन्ट्रैक्ट रिसर्च संगठन है, जो क्लिनिकल परीक्षणों में सहयोग करता है और विशेष रूप से महत्वपूर्ण चरण 2 और चरण 3 अध्ययनों पर ध्यान केंद्रित करता है। इसका कार्य सूजन संबंधी आंत्र रोग, ऑन्कोलॉजी, हेमेटोलॉजी, संक्रामक रोगों, मल्टीपल स्क्लेरोसिस और दुर्लभ रोगों सहित विभिन्न उपचार क्षेत्रों में फैला हुआ है। कंपनी क्लिनिकल परीक्षणों की योजना बनाने और वित्तीय निगरानी के लिए एक स्वामित्व वाले प्लेटफ़ॉर्म का उपयोग करती है, जिससे टीमें अध्ययन की समयसीमाओं और बजट पर नज़र रख सकती हैं। PSI CRO AG की प्रोफ़ाइल स्वास्थ्य सेवा और परामर्श विशेषज्ञता को गुणवत्ता, अनुकूलता और विश्वसनीय परीक्षण संचालन पर ज़ोर देने के साथ जोड़ती है।

Clinical Research Associate II in Australia

Lead clinical trial monitoring and site management across Australia, supporting study start-up, regulatory submissions, data quality, and patient safety for PSI CRO AG.

विवरण

  • Conduct and document onsite monitoring visits across clinical trials
  • Support study start-up activities
  • Review case report forms, verify source data, and resolve queries
  • Coordinate site budgets and contract negotiations
  • Track study progress at the country level
  • Manage communication and ongoing relationships with clinical sites
  • Coordinate with internal support functions and external vendors
  • Update project teams on study progress and operational matters
  • Contribute to feasibility assessments and research
  • Assist regulatory colleagues with study submission documentation
  • Oversee clinical activities for full-service global projects in Australia
  • Maintain study timelines, targets, and applicable clinical research standards
  • Develop productive relationships with investigators and research sites
  • Protect participant rights, safety, and well-being while maintaining data quality and compliance

आवश्यकताएँ

  • Degree in life sciences, pharmacy, nursing, or a comparable combination of education, training, and experience
  • At least two years of independent onsite monitoring experience in Australia
  • Experience conducting Phase II and/or Phase III monitoring visits
  • Background in inflammatory bowel disease, oncology, or infectious diseases is advantageous
  • Professional working proficiency in English
  • Working knowledge of Microsoft Word, Excel, and PowerPoint
  • Strong planning and multitasking abilities in a dynamic team setting
  • Effective communication, collaboration, and problem-solving skills
  • Willingness and ability to travel

लाभ

  • Competitive compensation
  • Hybrid schedule with two flexible days and three office days
  • Access to an onsite gym
  • Five additional wellness-leave days
  • Professional development and learning opportunities
  • Opportunity to contribute to the clinical research industry
  • Ongoing support from colleagues worldwide
  • Practical learning through day-to-day work
  • Structured development programs
  • Multiple paths for continued career growth

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