Responsibilities

Asegúrese de leer detenidamente la información sobre esta posibilidad antes de presentar su candidatura.

(a) Site management

- Study site selection, initiation (SIV) and clinical monitoring.

- Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

- Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

- Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

- Track study recruitment to ensure recruitment target is achieved in all studies.

- Conduct monitoring visit according to SDV plan and SOP;
address issues with sites and complete monitoring visit report in a timely manner coordinating.

- Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

- Assemble site specific EC submission dossier, and ensure submission to EC.

Training

- Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.





- Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

- Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

- Prepare/complete study records' archiving according to protocol and sponsor requirements.

(b) Drug Safety

- Ensure safety information is disseminated to all sites according SOP and applicable regulations.

- Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

- Finalize budget and obtain signed contract from site, prior to site initiation visit.

- Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

- Update and maintain Study tools/systems in a timely manner. xhfqzwm

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.

3.2 At least 8 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

📌 Contractor Cra_spain (Foz)
🏢 Tigermed
📍 Foz