Site Management Associate
2 dni temu
An exciting opportunity has arisen for a highly motivated and organized individual to join our team as an Associate Site Manager at TN Poland.
About the Role:The Associate Site Manager will serve as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
This role requires strong communication and organizational skills, as well as a willingness to travel occasionally. The ideal candidate will have a minimum of 1 year of clinical trial monitoring experience and a basic working knowledge of GCP, company SOPs, local laws, and regulations.
We are looking for someone who is proficient in speaking and writing English and has strong IT skills in appropriate software and company systems.
Key Responsibilities:
- Acts as primary local company contact for assigned sites for specific trials.
- May participate in site feasibility and/or Site Qualification Visit.
- Attends/participates in investigator meetings as needed.
- Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
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