Thermo Fisher Scientific
Thermo Fisher Scientific
Thermo Fisher Scientific ऐसी प्रौद्योगिकियाँ, प्रयोगशाला उत्पाद और फार्मास्युटिकल सेवाएँ विकसित तथा उपलब्ध कराती है, जो वैज्ञानिक अनुसंधान और स्वास्थ्य सेवा को समर्थन देती हैं। इसका कार्य जीवन विज्ञान अनुसंधान, विश्लेषणात्मक समस्याओं के समाधान, प्रयोगशाला उत्पादकता, निदान तथा उपचारों के विकास और निर्माण तक फैला हुआ है। कंपनी Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon और PPD सहित विभिन्न ब्रांडों के पोर्टफोलियो तथा एक वैश्विक टीम के माध्यम से ग्राहकों की सेवा करती है। इसके करियर अवसर इन उत्पादों और सेवाओं से जुड़ी वैज्ञानिक, स्वास्थ्य सेवा, विनिर्माण, लॉजिस्टिक्स और सेवा संचालन को शामिल करते हैं।

Clinical Study Planning and Scheduling Lead - Texas Remote

Senior clinical scheduling lead overseeing early-phase study placement and portfolio planning across Thermo Fisher Scientific research units. Coordinates capacity, protocols, calendars, and cross-functional scheduling decisions.

विवरण

  • Direct early-phase study planning and portfolio scheduling across the Austin, Las Vegas, and Prague Clinical Research Units
  • Manage integrated calendars for awarded and prospective clinical studies
  • Assess study placement and timing using protocol requirements, participant and cohort needs, bed capacity, recruitment capabilities, procedures, equipment, holidays, sponsor deadlines, and competing site activity
  • Manage calendar updates, evaluate portfolio effects, apply routine changes, and escalate material capacity decisions
  • Lead study placement and scheduling discussions with site leaders, investigators, recruitment, business development, finance, and clinical operations
  • Coordinate portfolio schedules across Clinical Research Units, including multisite studies
  • Maintain scheduling records, trackers, and planning tools supporting capacity planning, revenue forecasts, and business decisions
  • Administer Human Safety Committee activities, including submissions, reviews, agendas, meetings, minutes, decisions, and follow-up
  • Coordinate study placement within Clinical Research Units, record decisions and action items, and keep calendars current
  • Engage clients on scheduling factors, capacity limitations, and available alternatives

आवश्यकताएँ

  • Bachelor’s degree or equivalent combination of formal academic or vocational qualifications
  • Comparable professional experience of 0–2 years
  • Working knowledge of clinical trial processes, particularly early-phase research and Clinical Research Unit operations
  • Capability to review study protocols and determine scheduling and placement needs
  • Strong written, verbal, and interpersonal communication skills
  • Advanced presentation and meeting facilitation abilities
  • Highly organized approach with careful attention to detail
  • Effective time management and prioritization across multiple concurrent activities
  • Professional judgment and business maturity
  • Ability to work effectively both independently and with a team
  • Capacity to work in office, laboratory, and clinical settings
  • Proficiency with a range of internal and commercial software applications
  • Ability to remain upright or stationary for 6–8 hours daily
  • Ability to move frequently, including bending, twisting, crouching, and stooping
  • Ability to lift and carry 15–20 pounds
  • Reliable and consistent attendance
  • Ability to multitask and maintain performance under stress

लाभ

  • Work within a globally distributed team
  • Opportunities for collaboration and professional development
  • Workplace centered on scientific excellence

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