About the role:
You will develop, negotiate, and finalise site agreements and budgets for medical device clinical trials in a variety of therapeutic areas by collaborating with internal key stakeholders and working with external health care institution staff.
Your responsibilities will include:
- Preparation, negotiation, analysis, escalation, and finalisation of all site agreements and budgets.
- Accelerate negotiations by using budget parameters
- Working with legal stakeholders to negotiate contracts
- Maintain regular communication and escalation to expedite the planning, execution, issue resolution, and management of Site/Investigator agreements.
- Understand Site Activation requirements versus contracting turnaround times to support study site authorisation
Required qualifications:
- Bachelor's degree, or equivalent experience
- Minimum of 2 years Industry experience managing clinical site contracts & budgets
Preferred qualifications:
- Demonstrates effective time management skills, including the ability to prioritise multiple tasks independently
- Demonstrates the ability to work independently and take initiative to prevent and resolve issues
- Demonstrates the ability to have strong analytic and organisational skills
- Demonstrates the ability to communicate effectively in English, both in writing and orally
- Demonstrates interpersonal skills demonstrated by being proactive, customer-focused, and independent critical thinker
