(Senior) Site Activation Specialist

Currently seeking a (Senior) Site Activation Specialist 1 who has prior start up experience to join our sponsor-dedicated team. You will execute feasibility, site identification, regulatory, start-up, and maintenance activities under moderate supervision. Prepare and manage site documentation, review and negotiate site documents and contracts, maintain site performance metrics, and serve as the primary contact for investigative sites. Ensure contracts are fully executed and establish project timelines. While you will be expected to conduct site selection visits and prior experience would be beneficial, it is not essential. This is a 12 month fixed term contract position.

When you join IQVIA AUSTRALIA in our sponsor-dedicated team, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.

With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

You must have a minimum of 3 years experience to be considered for this role. We regret to inform you that we cannot consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.

You will be asked to complete a short video screening as part of the interview process.

Sydney and Melbourne are preferred location but other Australian cities can be considered.

Essential Functions:

• Act as Single Point of Contact (SPOC) for site activation and maintenance activities.
• Collaborate with Site Activation Manager (SAM), Project Management, and other departments.
• Review and prepare site documents for accuracy.
• Inform team members of document completion.
• Distribute documents to sites and internal teams.
• Update internal systems and project plans with accurate information.
• Track and follow up on required documents' progress and approval.

Qualifications:

• Bachelor's Degree in Life Sciences or related field.
• 3 years of clinical research in start up or relevant experience, or equivalent education and training.
• 3 years of experience in a healthcare environment or equivalent.