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
Senior International Talent Acquisition Officer
Senior International Talent Acquisition Officer
We regret to inform you that this job opportunity is no longer available as it has expired
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