Data Manager for Clinical Trials

PSI CRO; Lombardia; In loco; EUR 34.000 - 52.000; Tempo pieno

Descrizione del lavoro

PSI CRO, a leading Contract Research Organization, is seeking a detail-oriented Clinical Data Manager to manage clinical data effectively. You will track database setup, data entry, and ensure data quality throughout various projects.

The ideal candidate will have a University degree, proficiency in clinical data systems, and strong organizational skills. The position offers a salary range of €34,000–€52,000 annually, depending on experience and competencies.

Join PSI CRO and be part of a diverse community dedicated to advancing pharmaceutical research.

Competenze

• Demonstrated experience of managing clinical or medical data.
• Ability to work independently and multi-task.

Mansioni

• Track database set-up, testing, maintenance and data entry.
• Communicate with clients, project teams and vendors on data management matters.
• Design eCRF, Data Management and Data Validation Plans and test EDC databases.
• Train site staff and project teams on CRF completion and data management topics.

Conoscenze

Attention to detail

Proficiency in MS Office

Organisational skills

Time management skills

Full working proficiency in English

Formazione

College/University degree (Life Sciences, Pharmacy)

Strumenti

Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)

Descrizione del lavoro

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.

Please submit your CV in English

Responsibilities

• Track database set-up, testing, maintenance and data entry
• Communicate with clients, project teams and vendors on data management matters
• Review study documents, design and develop project specific guidelines and instructions
• Design eCRF, Data Management and Data Validation Plans and test EDC databases
• Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation
• Code medical data
• Track and report metrics leading to database lock
• Coordinate the processing, dispatch and archiving of CRFs/queries
• Maintain Clinical Data Management working files
• Perform database QC checks, prepare and attend audits
• Train site staff and project teams on CRF completion and data management topics

Qualifications

• College/University degree (Life Science, Pharmacy degree is a plus)
• Demonstrated experience of managingclinical or medical data
• Full working proficiency in English
• Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)
• Proficiency in MS Office applications
• Organisational and time management skills
• Ability to work independently and multi-task

Base salary range: €34,000–€52,000 gross annual salary.
Actual compensation: The salary offered within the stated range will depend on objective, job-related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.
Additional compensation: bonus, incentive plans, and other benefits may apply.