Senior SAS Developer (SDTM)

PSI CRO AG; Milano; In loco; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

A global leader in clinical research, PSI CRO AG, seeks a knowledgeable and proactive Senior Database Developer to join their Data Management team. In this full-time role, you'll focus on high-quality clinical database development and programming, ensuring data accuracy and compliance in clinical trials, while collaborating with clients and vendors.

Competenze

• Full professional proficiency in English required.
• Relevant technical experience in clinical data management or related fields.
• Experience working with clinical or medical data in a professional environment.

Mansioni

• Serve as a communication point for data management and programming.
• Review and test clinical database requirements.
• Validate clinical trial data according to SDTM standards.

Conoscenze

SAS programming

SQL

Data validation

Clinical data management

CDISC standards

Formazione

College or University degree in IT, programming, or technical field

Strumenti

Clinical Data Management systems (e.g., Medidata, Veeva)

MS Office

MS Access

Descrizione del lavoro

6 days ago Be among the first 25 applicants

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.

Please note the official PSI CRO job title will be : Senior Database Developer. If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!

Responsibilities :

• Serve as a communication point for data management and statistics on database programming and deliverables.
• Review and test clinical database (EDC) requirements and structure.
• Review data validation plans and program data validation procedures.
• Generate clinical database listings and reports to support data collection, tracking, review, and validation in clinical trials.
• Participate in developing Study Data Tabulation Model (SDTM) including define.xml, annotated CRF, reviewer’s guide, and program data transformation into CDISC-compliant formats.
• Validate clinical trial data according to SDTM standards.
• Transfer deliverable databases to clients electronically.
• Liaise with vendors and clients regarding electronic data transfer specifications.

Qualifications :

• College or University degree in IT, programming, or technical field.
• Full professional proficiency in English.
• Relevant technical experience in clinical data management or related fields.
• Experience with Clinical Data Management systems (e.g., Medidata, Veeva) is desirable.
• Proficiency in SAS programming (Base SAS, SAS / Macros, SAS / ODS).
• Knowledge of CDISC standards.
• Experience with SQL.
• Proficient in MS Office applications and MS Access.
• Experience working with clinical or medical data in a professional environment.

Additional Information :

If you wish to showcase your skills and knowledge within a growing company that values its people, this is the right opportunity for you.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Information Technology
• Pharmaceutical Manufacturing

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