Participation of pre award and big defense meeting activities providing start up expertise input for the project strategy.
Upon award, develop the site activation delivery strategy according to project scope and specifics, indicating the activation projection for sites in diverse countries, site identification, regulatory, contract and start up elements’ timelines.
Oversee the execution of global site activation strategy, focusing in delivering sites in the agreed timeline, budget and within scope, pro-actively identifying and addressing risks.
Communication with client, project team members and local regulatory specialists on study sites status, activation projections, risks, and opportunities to secure the activation strategy.

Must have a Bachelor's Degree Life sciences or related field.
At least 5
7 years global experience in a clinical research environment.
Strong leadership competencies to lead projects and multi-cultural teams.
Project ownership controlling delivery on time, within scope and controlling budget.
Demonstrable experience working on multiple projects or clients balancing competing priorities
Strong communication skills with the ability to negotiate and challenge decisions.
Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects.
Proven ability to establish and maintain effective working relationships with co-workers, managers, and sponsors.

Associate Site Activation Manager

Key skills