Site Identification Specialist at PSI CRO

Oxford, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

06 May, 26

Salary

0.0

Posted On

05 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Identification, Clinical Trials, Relationship Building, Project Management, Good Clinical Practice, Regulatory Compliance, Data Management, Communication, Problem Solving, Team Collaboration, Due Diligence, Risk Assessment, Dynamic Environment, Monitoring Experience, Study Startup, Clinical Operations

Industry

Pharmaceutical Manufacturing

Description

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 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. 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. 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 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 Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization.

Responsibilities

The Site Identification Specialist is responsible for developing strategic relationships with clinical research sites to optimize clinical trials. This includes conducting site identification activities, maintaining databases, and collaborating with project teams.