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 will include:

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

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