Site Identification Specialist at PSI CRO

Belgrade, Central Serbia, Serbia -

Full Time

Start Date

Immediate

Expiry Date

27 May, 26

Salary

0.0

Posted On

26 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Identification, Relationship Building, Clinical Trials, Database Maintenance, Study Startup, Protocol Discussion, Site Evaluation, Risk Identification, Due Diligence, Regulatory Compliance, Legal Limitations, Cross-functional Collaboration, Project Management, English Proficiency

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with over 30 years of experience in the industry, offering a strong balance between long-term stability and continuous innovation for both clients and employees. We are committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Belgrade, Serbia This is the main responsibility of a site ID specialist Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement Project Responsibilities: Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials. Define the main study objectives and the optimal site profile Create initial list of potential sites Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities 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 In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed Qualifications University/college degree (MD/PharmD degree), or an equivalent combination of education, training and experience On-site monitoring experience is a plus Understanding of Good Clinical Practice, local laws and applicable regulations in the region Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements Advanced English skills You are dynamic. You are curious. You are more than your job. For you, excellence isn’t just a word; it’s the measure for all you do. You’re passionate. Driven. Dedicated. You can’t stand mediocrity. And you might be the team member we're looking for. Additional Information What we offer: Excellent working conditions. Extensive training and friendly team. 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. You will be on the frontline of the new medications development and will work closely with cross-functional experts to drive your startup projects forward.

Responsibilities

The main responsibility involves communicating and building relationships with clinical research sites to identify potential centers for clinical trials. This includes conducting site identification activities, defining study objectives, creating initial site lists, and maintaining relevant trackers during the trial startup phase.