Greece Job Openings
Excelya
Clinical Data Manager I
FULL TIME
October 29, 2024
The Position:
Excelya is currently seeking to hire a Clinical Data Manager (CDM), who will be responsible for performing Data Management tasks per client work orders to high regulatory standards and Excelya Group SOPs.
Responsibilities/Tasks
Excelya is currently seeking to hire a Clinical Data Manager (CDM), who will be responsible for performing Data Management tasks per client work orders to high regulatory standards and Excelya Group SOPs.
Responsibilities/Tasks
- Deeply acknowledges and strictly follows Excelya and Client’s SOPs, guidelines and appropriate local and international legislation.
- Ability to work under the supervision of more senior staff (Manager or Senior CDM).
- Responsible for data cleaning, data review, discrepancy management and data reconciliation activities on the assigned studies.
- Closely collaborate with the Lead Data Manager responsible for the clinical studies.
- Able to produce study metrics and status reports for individual studies and across multiple studies
- Actively participated in EDC database build and testing through go live.
- Responsible for completing Excelya administrative tasks as required e.g., timesheets, CV and training updates.
- May undertake additional tasks assigned by the supervisor related to any of the Excelya Group companies
- Holds a Bachelor’s degree in Life Sciences or similar one.
- At least 1 year of working experience in the position of Clinical Data Manager or equivalent combination of education, training and experience
- Holds an extensive knowledge and understanding of ICH GCP, along with other relevant ICH, EU, and FDA guidelines, to ensure and maintain regulatory compliance.
- Strong understanding of recommended best practices in Clinical Data Management (CDM) and the associated documentation requirements
- Responsible for managing clinical trial databases and applications, clinical data flow management, data review processes, and e Case Report Form (e CRF) design
- Solid understanding of clinical trials and the study lifecycle, including start-up, maintenance, and closeout phases.
- Proficient in office technology and software, including Word, Excel, Power Point, MS Project, and other relevant tools.
- Ability to maintains high level of professionalism, ethics and compliance at all times.
- Fluent in both written and spoken Greek and English
Summary
-
Type of job:
Full-time -
Location:
Greece -
Capability:
Data Management
Contact
Anastasia Matsoukopetrou
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