Site Liaison Coordinator

2 days ago


Pretoria, Gauteng, South Africa PSI CRO Full time
About Us
As a leading Contract Research Organization, we offer extensive training and friendly team environment. Our company was founded in 1995 and has grown to become a dynamic, global entity with over 2,700 driven employees worldwide.

Job Description
The successful candidate will be responsible for maintaining and generating relations with Investigative Sites. This will include maintaining and refining internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement. Additionally, the candidate will participate in the development of improvement strategies for the site identification process, implementation thereof, as well as related training activities.

Key Responsibilities:
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. Perform due diligence check of regulatory and legal 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, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed.

Requirements:
University/college degree (Life Sciences/Pharmacy/RN/Healthcare field is a plus), or an equivalent combination of education, training and experience. Minimum 10 years of proven prior experience in Site Identification/Feasibility/Study Start-Up activities/Site Monitoring. Understanding of Good Clinical Practice, local laws and applicable regulations in the region. Full working proficiency in English. Communication and collaboration skills. Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements.

We Offer
Excellent working conditions, competitive salary and benefits package, and extensive training.

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