Associate, Study Management III
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Job Location:
Monthly Salary:
Posted on:
20 hours ago
Vacancies:
1 Vacancy
Job Summary
Supporting the Study Project Manager in strategic leadership of the cross-functional team through stakeholder engagement and influence to drive deliverables and timelines including study-level oversight and leadership of assigned activities within one or more global trials in a cross-functional environment for activities from inception through closure. Vendor management from initiation through closure including deliverable oversight and risk management for one or more vendors. Recruitment management from country feasibility through subject recruitment and retention. Leadership of assigned meetings and training (internal and external) and provision of regular updates on study status e.g. agenda and minutes. Ensure inspection readiness and participate in related activities. Risk identification mitigation and -development and management of study materials and systems throughout study life cycle (e.g. Protocols informed consent clinical study report training materials newsletters presentations IP CTMS eTMF EDC IRT ePRO access management etc.) Provide engaging training to identified stakeholders as needed. Support process improvement initiatives.
Qualifications :
Bachelors Degree or OUS equivalent required 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 to support smart decision making 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:
No
Employment Type :
Full-time
Key Skills
- Portfolio Management
- Wealth Management
- Financial Services
- Hybris
- Microsoft Word
- Banking
- Cash Management
- Data Management
- Microsoft Powerpoint
- Securities Law
- Microsoft Excel
- Internet Of Things
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
