Study Management Associate III

Purpose

As a Study Management Associate III you will be part of a dynamic centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team.

The Study Management Associate III works as an independent contributing member of a cross-functional and global partnership to plan execute and manage one or more Phase 0-4 clinical trials under the guidance of the Study Project Manager and SMA Manager. The Study Management Associate III works to ensure that assigned studies are executed with quality and efficiency in accordance with timelines and budget to support broader company strategic objectives. The Study Management Associate III is expected to work in accordance with all AbbVie Ways of Working.

This is a global role and may be located virtually.

Responsibilities

• The Study Management Associate III is expected to work independently as a clinical study leader and contributor with appropriate support from the Study Project Manager on the following activities in compliance with quality standards (ICH/GCP Global Regulations and AbbVie policies and procedures):
• Study-level oversight and leadership of one or more global trials in a cross-functional environment for activities from inception through closure connecting functional work and strategic work across the global study including but not limited to:
• o Supports the Study Project Manager in strategic leadership of the cross-functional team through stakeholder engagement and influence to drive deliverables and timelines including strategy development meeting facilitation and timely documentation at the study level to drive for timely execution of clinical trial(s)
• o Vendor management including Request for Proposal (RFP)/initiation selection Scope of Work development & review deliverable oversight and risk management for one or more external vendors e.g. central lab recruitment imaging internal and external committees
• o Recruitment management including thoughtful review of intelligence data leadership cross-functional development and execution of recruitment strategies and mitigation planning on a global scale from country feasibility through subject recruitment and retention
• o Leadership of assigned meetings (cross-functional (internal) vendor and/or investigator) and provision of regular updates on study status e.g. agenda development minutes curation and filing. o Ensure inspection readiness and participate in related activities. Risk identification mitigation and management including timely issue review escalation and management to support trend analysis and risk prevention.
• Co-development and management (review revision tracking and filing) of study materials including but not limited to:
  o Protocols regulatory submissions patient reported outcome measures study execution plan informed consent site budgets and agreements clinical study report training materials newsletters presentations for various stakeholders
  o CTMS and eTMF management to ensure compliance/inspection readiness support trend analyses and support timelines
• o EDC IRT and ePRO which includes review of design specifications participation in user acceptance testing and contribution to development and review of associated plans and key risk indicators as well as system management activities like access support query resolution and oversight. Management of investigational product and other associated study supplies.
• Provide engaging training to identified stakeholders as needed e.g. study team members vendors. Support global submission strategies. Support process improvement initiatives or serve as a subject matter expert and/or mentor.

Qualifications :

• Bachelors Degree.
• Must have at least 4 years of progressive Pharma-related/clinical research-related experience with a high level of core and technical competencies.
• Competent in application of standard quality procedures (SOP ICH/GCP Global Regulations)
• Experienced user of systems such as EDC IRT CTMS and eTMF
• Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives to actively develop strategies and drive smart decision making to support acceleration of study timelines and enable a well-run study.
• Excellent organizational and time management skills strong attention to detail.
• Exceptional interpersonal skills with ability to communicate effectively in a clear and persuasive manner in a global setting; proficient in business/technical English-language (oral and written)
• Proactive collaborative mindset
• Ability to work independently in a fast-paced global team environment
• Preferred: Exposure to study initiation through completion activities; global study exposure

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Yes

Employment Type :

Full-time

Experience: years
Vacancy: 1