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7 часов Π½Π°Π·Π°Π΄

Clinical Lead (Clinical Trial Management) - Oncology - Global Study Leadership

Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
lead
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
Bulgaria
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR
Clinical Lead (Clinical Trial Management) - Oncology - Global Study Leadership (Clinical Trials/Oncology): Leading the clinical delivery of regional and global oncology studies with an accent on patient recruitment, site performance, clinical quality, and regulatory compliance. Focus on managing clinical risks, coordinating cross-functional stakeholders, and ensuring study milestones, budgets, and operational objectives are achieved.

Location: Sofia, Bulgaria

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead the clinical delivery of regional and global oncology studies against quality, timeline, recruitment, and operational objectives.
  • Drive patient recruitment and site engagement strategies to achieve enrolment targets.
  • Partner with Project Leaders and cross-functional teams to deliver milestones and resolve operational issues.
  • Guide clinical teams through resource planning, training, and study execution.
  • Manage clinical risks, quality standards, proactive mitigation, financial forecasting, budgets, and scope changes.
  • Support proposals, bid defence activities, continuous improvement, knowledge sharing, and development of less experienced team members.

Requirements

  • Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline.
  • At least 5 years of clinical research, monitoring, or clinical operations experience in a CRO, pharmaceutical, or biotechnology environment.
  • Strong understanding of clinical trial conduct, ICH-GCP guidelines, and applicable regulatory requirements.
  • Experience leading patient recruitment, site management, and clinical quality oversight.
  • Ability to collaborate across cross-functional teams and manage internal and external stakeholders in a global environment.
  • Strong communication, problem-solving, organizational, and decision-making skills.

Nice to have

  • Experience supporting project financial management and operational planning.

Culture & Benefits

  • Work across a diverse portfolio of therapeutic areas and global clinical studies.
  • Collaborate with experienced project leaders, clinical operations experts, pharmaceutical sponsors, and biotechnology sponsors.
  • Access mentorship, a collaborative global network, flexible ways of working, and career development opportunities.
  • Use AI-enabled technology and data-driven insights in clinical study delivery.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’