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Job Overview
The VP of Research Operation will be responsible for the operations of our growing number of clinical sites. This includes leading the obtaining of new clinical trials, development and implementation of the study protocols, recruiting and retaining study participants, and ensuring the highest quality and compliance standards. The VP of Research Operations will also build and maintain relationships with key stakeholders, including patients, investigators, sponsors, and regulatory agencies.
The Ideal Candidate:
Possess the ability to lead the site successfully along with leading its staff to actualize their individual potential to collectively grow the site.
- Independent critical thinker who can leverage resources to execute on mission critical objectives.
- Proven track record of achieving excellence
- Ability to operate independently in a deadline-driven, demanding workplace while being adaptive and paying attention to detail.
- Dynamic thinker who takes a multi-discplinary approach to solving problems.
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Key Responsibilities:
Study operations: Ensure studies are being executed successfully.
Patient recruitment and retention: Develop and implement strategies to recruit and retain study participants in collaboration with the study investigators and the study sponsor.
Quality assurance: Work with Director of QA to ensure the research site follows the study protocol, GCPs, and applicable regulations. Implement and maintain systems to ensure the integrity of the data.
Regulatory compliance: Ensure that the research site is in compliance with applicable regulatory requirements, including institutional review board (IRB) approvals and FDA regulations.
Staff management: Supervise and mentor the research site staff, ensuring that they are properly trained and qualified to perform their duties.
Stakeholder management: Build and maintain relationships with key stakeholders, including patients, investigators, sponsors, and regulatory agencies. Represent the research site at relevant meetings and conferences.
Budget and Resource Management: Plan and manage the research site budget, ensuring that resources are allocated efficiently and effectively.
Requirements
Qualifications:
- Minimum of 6 years of experience in a clinical research setting
- Strong understanding of GCPs and FDA regulations regarding the clinical trial process
- Experience in leading and managing clinical research studies
- Excellent organizational, communication, and leadership skills
- Strong problem-solving and critical-thinking abilities
- Ability to work independently and in a team environment
Benefits
- Dental insurance
- Flexible schedule
- Health insurance
- Paid time off
- Professional development assistance
- Relocation assistance
- Vision insurance
M1 Health
