Description
We are seeking a Site Activation Manager to direct and manage the execution of strategic, operational, and financial delivery of Site Activation activities. This includes Site ID and Selection, Ethics and Regulatory processes, and Site Contracting for assigned studies.
The successful candidate will provide strategic planning and project oversight to accelerate Site Activation through best-in-class project management. You will be accountable for multiple regions and support or participate in pre-award/bid defense activities.
Key Responsibilities:
- Oversee the execution of Start Up and Lifecycle Maintenance for assigned projects
- Develop, implement, and maintain the Site Activation Management Plan
- Collaborate with key stakeholders to deliver the agreed project scope in compliance with the Site Activation Management Plan
- Execute operational strategy and expectations for maintenance of clinical study approvals and authorizations
- Assess and review the regulatory landscape and contribute to the collection of accurate regulatory intelligence
- Determine regulatory strategy and expectations for submissions and authorizations
- Provide ongoing updates and reporting to various levels of the organization
- Ensure accurate completion and maintenance of internal systems, databases, and tracking tools
- Create and review technical and administrative documentation
- Mentor and coach colleagues as required
- May take a lead role in developing long-standing relationships with preferred IQVIA customers
- Deliver presentations and training to clients, colleagues, and professional bodies
Requirements:
- Bachelor's Degree in Life Sciences or a related field
- At least 5 years of experience with 2 years of lead experience in a scientific or clinical environment
- Demonstrable experience in an international role or equivalent combination of education, training, and experience
The potential base pay range for this role, when annualized, is $86,500.00 - $216,000.00.