CLINICAL DATA MANAGER

  • Pubblicato il 27/07/2026
  • Siena (SI)
  • Da definire

Descrizione:

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

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