PSI CRO
Healthcare
SiteIdentificationSpecialist
Neural analysis suggests this role is
optimal for mid candidates.
“Site Identification Specialist at PSI CRO. Skills: Site identification, Database management, Regulatory knowledge. Maintain and generate relations with Investigative sites. Maintain and refine internal site database”
Industry & Context.
What They're Looking For.
Must Have
University/college degree, Equivalent combination of education, training, and experience, Previous experience working with investigative sites, Experience with data analysis, Knowledge of Good Clinical Practice, Knowledge of local laws, Knowledge of applicable regulations in the region, Full working proficiency in English, Full working proficiency in Portuguese
Nice to Have
Life sciences/healthcare field degree, Equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities
What You'll Do.
Maintain and generate relations with Investigative sites
Maintain and refine internal site database
Participate in development of improvement strategies for site
Create initial list of potential sites
Communicate with project teams to define strategy and
Maintain study site identification process
Liaise with project teams to evaluate status and
Identify and highlight potential risks or issues
Perform due diligence check of regulatory limitations
Participate in project team meetings
Support the project team throughout study startup
How You'll Work.
Team & Collaboration
Cooperation with Study Startup; Cooperation with Clinical Operations; Cooperation with Process; Cooperation with project team; Project team meetings
Communication Scope
Written communication skills; Oral communication skills
Full Job Description
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. Please provide your CV in English. 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. ## Qualifications * 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, * Knowledge of Good Clinical Practice, local laws and applicable regulations in the region is a plus; * Full working proficiency in English and Spanish; Portuguese is a plus; * Excellent written and oral communication skills, as well as time management skills. ## Additional Information We offer: * Excellent and flexible working conditions * Extensive training and friendly, collegial
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