CLINICAL DATA MANAGER

Philogen S.p.A.; Siena; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Competitive salary

Job summary

A leading biotechnology firm in Tuscany is seeking a Clinical Data Manager to oversee data cleaning and management for clinical trials. The successful candidate will have a Master's degree, at least 2 years of experience in clinical research, and strong attention to detail. This full-time position involves designing CRFs, collaborating with clinical teams, and ensuring compliance with data standards. Competitive salary based on experience is offered.

Qualifications

• 2 years of experience with clinical trial research and data management.
• Ability to prioritize tasks and handle multiple projects.
• Knowledge of clinical research procedures and regulations.

Responsibilities

• Perform data cleaning activities on assigned studies.
• Design Case Report Forms (CRFs) in collaboration with the clinical team.
• Collaborate on the implementation and validation of clinical databases.

Skills

Attention to detail

Organizational skills

Cross-functional team collaboration

Data analysis skills

Effective communication

Education

Master's degree in healthcare or a related field

Tools

MS Excel

Coding dictionaries (e.g., MedDRA)

SAS

Job description

Direct message the job poster from Philogen S.p.A.

Philogen S.p.A. is a biotechnology company whose mission is the development of biologic products for the imaging and therapy of life‑threatening diseases, with a strategic focus on cancer diseases and rheumatologic disorders.

Philogen S.p.A. would like to hire a highly motivated and qualified Clinical Data Manager who will report to the Data Manager Coordinator.

Responsibilities

• Perform data cleaning activities on assigned studies
• Design paper and/or electronic Case Report Forms (CRFs) in collaboration with the clinical team
• Collaborate in the implementation and validation of clinical databases
• Prepare, maintain and archive data management documentation (e.g. Data Management Plan)
• Review all the clinical data listings and tables
• Ensure data management in accordance with applicable standards (e.g. CDISC), regulatory guidelines and company SOPs
• Participate in study team meetings
• Support the Pharmacovigilance department in SAEs reconciliation
• Review clinical study protocols and Clinical Study Reports
• Perform coding activities using medical dictionaries

Qualifications

• Master's degree in healthcare or a related field
• 2 years of experience with clinical trial research and data management
• Meticulous attention to detail
• Strong organizational skills
• Ability to prioritize tasks and handle multiple projects at once and stressful situations
• Ability to work in cross‑functional study team
• Knowledge of clinical research procedures and regulations
• Good knowledge of MS Excel and Office packages in general
• Good skills in data analysis
• Ability to communicate effectively (both verbally and writing)
• A clear understanding of the benefits of clinical trial research

Preferred skills

• Knowledge of medical terminology with expertise in oncology preferred
• Knowledge of coding dictionaries (e.g. MedDRA)
• SAS Knowledge

Benefits

• A contract and salary proportional to the experience (seniority) of the successful candidate.

Location & EEO Statement

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.

Seniority level: Associate

Employment type: Full‑time

Job function: Research

Industry: Pharmaceutical Manufacturing