Lead Data Manager – Clinical Trials

🕒 February 20

🇧🇷 Brazil – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision • Primary communication point for project teams and company departments with regard to clinical data management • Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables • Primary responsibility for clinical data management activities within clinical projects • Study documents review • Data Management plan and other project-specific guidelines and instructions development and review • Co-ordinate/perform user acceptance testing • Development of Data Validation Plan/Edit Check Specifications • Data entry coordination and supervision • Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution • Non-CRF electronic data handling • Database edits (paper CRF studies) • Manual CRF review (non-medical checks) • Clinical database lock • Coordination and supervision of processing, dispatch and archiving of CRFs/queries • Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol • Development of CRF completion guidelines • Coding medical data with coding dictionaries and coding listings review • SAE reconciliation • Electronic data transfer specifications review and approval • Liaison with Document Center with regard to maintenance of TMF and eTMF • Database QC checks performance and documentation • Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management • Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management • Training of Assistant Data Managers • Project-specific training of investigators and clinical team in CRF completion

🎯 Requirements

• College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities • At least 3 years of experience of full scope of data management responsibilities in international EDC studies • At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable) • Project data management experience is a plus • Full working proficiency in English • Organizational and managerial skills

🏖️ Benefits

• Advance your career in clinical research and develop new skillsets whilst growing with the organization.