Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Job Description

If you are an experienced CRA, who have been mentoring junior staff and/or leading some project activities and feels it's time to take the next step, this opportunity is for you! 

In the role of Lead CRA, you will manage local CRAs, supervising clinical monitoring and site management activities to verify the protection of trial subjects’ rights, safety and well-being, data quality and study compliance on a country/regional level.

Only CVs in English will be considered.

You will:

Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules Train Monitors in annotated monitoring visit reportsReview monitoring reports and support monitors in their activitiesAct as the main communication line between Monitor and Regional Lead Facilitate site budgets and contract negotiationsBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progress and lead project team calls on the country level Participate in quality control and compliance monitoringMay need to monitor and manage sites (if applicable)May need to supervise monitors on siteOversee and maintain study-specific and corporate tracking systems at site and country level

QualificationsCollege/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experienceParticipation in clinical projects as a Lead/Senior MonitorAt least 4 years of experience as Senior CRAIndependent on-site monitoring experienceFull working proficiency in English and SpanishPC skills to be able to work with MS Word, Excel and PowerPointAbility to plan, multitask and work in a dynamic team environmentCommunication, leadership, and problem-solving skillsAbility to travel

Additional Information

Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.