Sr Site Activation Specialist / Contract Specialist

• B Sc Degree in Life Sciences or related field

• 3 years experience in clinical trial submissions, particularly MoH and Ethics Committee (CEC) initial applications, preferably gained within a CRO environment supporting multiple sponsors.

• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors

• Ability to work on multiple projects

• Bachelor's Degree in Law or related field

• Candidate with legal background who has 3 years experience in clinical trial contracts

• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors

• Ability to work on multiple projects

Support country-level activities related to site activation, start-up, and clinical trial agreements (CTAs). This role plays a key part in ensuring timely study initiation, compliance with regulations, and effective contract and budget management. As a Senior Site Activation Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs), Work Instructions, quality of designated deliverables and project timelines. You will perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions, along with distributing completed documents to sites and internal project team members.

• Exposure across 21 Therapeutic Areas

• Be part of a global team who operate across 141 locations

• Exposure across a variety of studies and projects

• Access to new, innovative technologies

• Work within a collaborative and vibrant environment

• Own your career!

It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.