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 3000 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.
As a Site Laboratory Specialist at PSI, you will be responsible for:
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
The Senior Start Up Associate manages study start-up activities at country and site levels, ensuring compliance with regulatory requirements and facilitating timely site activation.
Maintains Trial Master Files for assigned clinical research projects, overseeing document processing, indexing, quality checks, reporting, audit support, and study-closeout reconciliation and archiving.
Manage and optimize COA/eCOA systems for clinical trials, coordinating licensing, translations, testing, deployment, integrations, vendor oversight, and ongoing support with study teams and stakeholders.
Manage behavioral health insurance authorizations for PHP and IOP treatment, coordinating reviews, appeals, and payer requirements to support medical necessity and continuity of care.
Conduct brief clinical intake consultations with adolescents and caregivers, assess safety and treatment needs, guide families toward appropriate PHP or IOP care, and coordinate next steps with clinical teams.
