Study Management Associate III

hace 5 días

Madrid, Madrid, España Abbvie A tiempo completo
Job Description

Job Summary: We are seeking a highly skilled and experienced Study Management Associate III to join our dynamic and centralized study management team at AbbVie. As a key member of the study team, you will be responsible for the execution of our global clinical trials and will work closely with cross-functional partners to plan, execute, and manage Phase 0-4 clinical trials.

Key Responsibilities:

  • Provide strategic leadership to cross-functional teams to drive deliverables and timelines for global clinical trials.
  • Manage vendor relationships, including Request for Proposal (RFP) initiation, selection, and oversight of external vendors.
  • Develop and execute recruitment strategies and mitigation plans on a global scale.
  • Lead assigned meetings and provide regular updates on study status.
  • Ensure inspection readiness and participate in related activities.
  • Identify, mitigate, and manage risks to support trend analysis and risk prevention.
  • Develop and manage study materials, including protocols, regulatory submissions, and clinical study reports.
  • Manage EDC, IRT, and ePRO systems to ensure compliance and inspection readiness.
  • Provide training to stakeholders as needed.
  • Support global submission strategies and process improvement initiatives.

Requirements:

  • Bachelor's Degree or equivalent required.
  • At least 4 years of progressive Pharma-related/clinical research-related experience.
  • Strong analytical and critical thinking skills.
  • Excellent organizational and time management skills.
  • Exceptional interpersonal skills.
  • Proactive and collaborative mindset.
  • Ability to work independently in a fast-paced global team environment.

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