Site Identification Specialist

PSI CRO

11h•Remote

About The Position

PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. The scope of responsibilities will include: Constantly maintain and generate relations with Investigative Sites; Maintain and refine the internal site database in cooperation with Study Startup, Clinical Operations and Process Improvement; Participate in development of improvement strategies for the site identification process; Create the initial list of potential sites; Communicates with project teams to define strategy and methodology of initial and follow-up site contacts; In cooperation with the project team maintain a study site identification tracker; Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives; Perform due diligence check of regulatory limitations applicable to the recommended investigators or clinical sites. Participate in project team meetings during study startup, as needed; Support the project team throughout study startup and further on.

Requirements

University/college degree (life sciences/healthcare field is a plus), or an equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities
Previous experience working with healthcare
Experience with data analysis
Full working proficiency in English and Spanish

Nice To Haves

Knowledge of Good Clinical Practice, local laws and applicable regulations in the region is a plus
Portuguese is a plus
Excellent written and oral communication skills, as well as time management skills

Responsibilities

Constantly maintain and generate relations with Investigative Sites
Maintain and refine the internal site database in cooperation with Study Startup, Clinical Operations and Process Improvement
Participate in development of improvement strategies for the site identification process
Create the initial list of potential sites
Communicates with project teams to define strategy and methodology of initial and follow-up site contacts
In cooperation with the project team maintain a study site identification tracker
Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
Perform due diligence check of regulatory limitations applicable to the recommended investigators or clinical sites
Participate in project team meetings during study startup, as needed
Support the project team throughout study startup and further on