Data Manager for Clinical Trials (Turbigo)

Data Manager for Clinical Trials (Turbigo)

31 lug
|
Psi Cro
|
Turbigo

31 lug

Psi Cro

Turbigo

ppPSI 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. /p pAt 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. /p pWe 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. /p h3Job Description /h3 pClincial 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. /p h3Responsibilities /h3 ul liTrack database set‑up, testing, maintenance and data entry /li liCommunicate with clients, project teams and vendors on data management matters /li liReview study documents, design and develop project specific guidelines and instructions /li liDesign eCRF,



Data Management and Data Validation Plans and test EDC databases /li liEnsure data entry, follow‑up and validation, including manual CRF review and SAE reconciliation /li liCode medical data /li liTrack and report metrics leading to database lock /li liCoordinate the processing, dispatch and archiving of CRFs/queries /li liMaintain Clinical Data Management working files /li liPerform database QC checks, prepare and attend audits /li liTrain site staff and project teams on CRF completion and data management topics /li /ul h3Qualifications /h3 ul liCollege/University degree (Life Science, Pharmacy degree is a plus) /li liDemonstrated experience of managing clinical or medical data /li liFull working proficiency in English /li liExperience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) /li liProficiency in MS Office applications /li liOrganisational and time management skills /li liAbility to work independently and multi‑task /li /ul h3Additional Information /h3 pbBase salary range: /b €34,000–€52,000 gross annual salary.br/bActual compensation: /b The salary offered within the stated range will depend on objective, job‑related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.br/bAdditional compensation: /b premio, incentive plans, and other benefits may apply. /p /p #J-18808-Ljbffr

📌 Data Manager for Clinical Trials (Turbigo)
🏢 Psi Cro
📍 Turbigo

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