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Clinical Research Associate

PanaCRO

Australia · Tam zamanlı

Başvuran ilk kişi siz olun

Deneyim
3–10 yrs
Maaş
Açılışlar
1
Yayınlandı
14 saat önce
Çalışma modu
Ofiste
Eğitim
Bachelor's degree in biomedical or science discipline
Sürdürmek
Başvuru yapılması gerekmektedir.

İş tanımı

About the Company

Panacro Pharmaceutical Technology Co., Ltd. is a contract research organization (CRO) specializing in pharmaceutical research and development along with clinical studies. Since its inception in 2004, the company has supported numerous clients domestically and internationally across over 20 key therapeutic areas. Panacro operates with a professional team adhering to international standards (ICH-GCP) and has established strong collaborations with approximately 80% of clinical study sites in China, complemented by a network of offices in over 20 provinces and cities. The organization emphasizes delivering high-quality, efficient services to accelerate clinical product market entry.

Key Responsibilities

  • Manage and oversee all aspects of clinical trials throughout every stage of the study process.
  • Develop protocols and necessary documentation to secure timely ethics committee (EC) approval.
  • Monitor and coordinate the clinical trial process, ensuring strict compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs).
  • Support resolution of queries, assist site closure activities, and gather documentation required for clinical trial reporting post-study completion.
  • Keep Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS) promptly and accurately updated per requirements.
  • Ensure timely reporting and follow-up of serious adverse events (SAEs) and adverse drug reactions in line with internal SOPs.
  • Maintain updated investigator files and trial master files.
  • Foster positive and collaborative relationships with clinical sites and investigators.
  • Complete site visit reports and related correspondence within designated timeframes.

Qualifications and Skills

  • Bachelor’s degree in biomedical or science disciplines such as BSc, Registered Nurse, or BPharm, or equivalent.
  • Experience ranging from 3 to 10 years in clinical operations monitoring, particularly for senior-level roles.
  • Proficiency in English.
  • Strong communication and organizational capabilities.
  • Demonstrated proactive attitude and effective work ethic.

Work styles they’re looking for

Etkili İletişim Organizasyon Becerileri Proactive work attitude

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