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PSI CRO AG

Data Manager – Clinical Trials

PSI CRO AG

Data Manager for Clinical Trials managing data for clinical research projects at a leading CRO. Ensuring quality and compliance in data management processes for various therapeutic indications.

Posted 7/1/2026full-timeRemote • 🇲🇽 MexicoMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Data Management, including database setup, testing, and maintenance, while ensuring data integrity through validation and quality checks. Proficient in training teams on data management practices and effectively communicating with stakeholders.

Highest-signal resume keywords
Clinical Data ManagementDatabase Setup and MaintenanceData Validation PlansMedidata RaveOracle InForm

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data EntryMedical Data CodingDatabase QC ChecksCRF ReviewSAE Reconciliation
Soft Skills
Organisational SkillsTime ManagementCommunication SkillsAbility to Work IndependentlyMulti-tasking
Tools & Technologies
MS Office ApplicationsEDC Databases
Industry Keywords
Clinical TrialsLife SciencePharmacy

Tech Stack

Tools & technologies
Oracle

About the role

Key responsibilities & impact
  • 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

Requirements

What you’ll need
  • College/University degree (Life Science, Pharmacy degree is a plus)
  • Demonstrated experience of managing clinical 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

Benefits

Comp & perks
  • Flexible work arrangements