Amy Hall
North Sutton,NH
Summary
Versatile and knowledgable clnical trial associate seeking a full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Overview
5
5
Years of clinical trial experience
Work History
Sr. Clinical Trial Associate
Mustang Bio
Worcester, MA
11.2021 - 05.2023
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Demonstrated strong organizational and time management skills while managing multiple projects.
- Used critical thinking to break down problems, evaluate solutions and make decisions.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Interacted respectfully with others to offer ideas, identify issues, and provide assistance.
- Demonstrated creativity and resourcefulness through the development of innovative solutions.
- Demonstrated respect, friendliness and willingness to help wherever needed.
- Participated in team projects, demonstrating an ability to work collaboratively and effectively.
- Identified plans and resources required to meet project goals and objectives.
- Coordinated with cross-functional teams to resolve project issues and mitigate risks.
- Provided detailed project status updates to stakeholders and executive management.
- Negotiated and managed third-party contracts related to project deliverables.
- Developed and implemented project plans and budgets to ensure successful execution.
- Monitored project progress, identified risks and took corrective action as needed.
- Sourced, vetted and managed vendors needed to accomplish project goals.
- Scheduled and facilitated meetings between project stakeholders to discuss deliverables, schedules and conflicts.
Education
Master of Science - Biotechnology
05.2014
Skills
- Site and Study Management
- Trial management
- Vendor Selection and Management
- Informed consent
- Research SOPs development
- Good Clinical Practices
- Multitasking abilities
- Self-motivated professional
- Interpersonal Communication
- Clinical Trials and Research
- Regulatory Requirements
- Clinical Data Collection
- Vendor Contracts
- Lab Specimens and Collections
- Trial Oversight
- Site and Study Management