BeOne Medicines
BeOne Medicines
BeOne Medicines स्विट्ज़रलैंड में स्थित एक वैश्विक ऑन्कोलॉजी कंपनी है, जो ऐसे नवीन कैंसर उपचारों की खोज और विकास पर केंद्रित है जिनका उद्देश्य उपचारों की सामर्थ्य और उपलब्धता में सुधार करना है। इसके पोर्टफोलियो में रक्त संबंधी कैंसर और ठोस ट्यूमर के उपचार शामिल हैं। कंपनी की इन-हाउस क्षमताओं और बाहरी सहयोगों के माध्यम से विकसित की जा रही नई उपचार पद्धतियों की पाइपलाइन लगातार विस्तार कर रही है। छह महाद्वीपों में 11,000 से अधिक सहकर्मियों के साथ, BeOne Medicines दुनिया भर के रोगियों के लिए दवाओं की उपलब्धता बढ़ाने के लिए काम कर रही है।

Regional Clinical Trial Management Associate

Support regional clinical study delivery, trial documentation, study systems, and budgets at BeOne Medicines. The company develops cancer medicines and therapies.

विवरण

  • Assist the Regional Clinical Study Manager with regional study delivery and delegated study activities.
  • Help Clinical Research Associates and Study Start-up Specialists deliver studies within their countries.
  • Support trial feasibility, start-up, document preparation and review, sample tracking, and participant enrollment.
  • Update CTMS records; prepare ISF binders; collect and customize documents, including ICFs; and maintain the eTMF.
  • Apply relevant regulations and ICH guidelines.
  • Coordinate regional and country team meetings, including agendas and minutes.
  • Maintain SharePoint folders, distribution lists, eTMF, CTMS, and other study systems.
  • Help manage system access requests and user accounts.
  • Assist with study start-up and investigator meetings, and with TMF creation, review, and quality checks.
  • Help address regional or country clinical supply issues and support data cleaning.
  • Draft site newsletters and clinical trial correspondence.
  • Maintain public registry information and contribute to Clinical Study Reports.
  • Assist with operational risk identification, audits, inspections, tools, work instructions, and SOPs.
  • Help set up vendors and manage regional study budgets, purchase orders, payment follow-up, and accruals.

आवश्यकताएँ

  • At least one year of clinical research experience in biotechnology, pharmaceuticals, or a CRO.
  • Knowledge of clinical operations methods and the operational aspects of clinical study processes.
  • Experience with MS Office, eTMF, and CTMS.
  • A bachelor’s degree, preferably in a scientific or healthcare field, is preferred.
  • Some travel may be required.
  • Exceptions may be considered for candidates with relevant clinical operations experience.

लाभ

  • Eligible for an annual bonus plan in non-commercial roles.
  • Eligible for incentive compensation in commercial roles.
  • Discretionary equity awards.
  • Optional participation in the Employee Stock Purchase Plan.
  • Medical insurance.
  • Dental insurance.
  • Vision coverage.
  • 401(k) plan.
  • FSA/HSA accounts.
  • Life insurance.
  • Paid time off.
  • Wellness benefits.

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