Senior Clinical Data Manager - FSP

Parexel International; México; On-site; MXN 1,259,000 - 1,978,000; Full time

Benefits offered by this job

Remote work

Travel opportunities

Job summary

Parexel International seeks a Senior Clinical Data Manager in Mexico or Argentina to lead Data Management for global trials. You will collaborate with cross-functional teams to plan, execute and oversee DM activities across Phase 1–4 studies, ensuring data quality and regulatory compliance with minimal supervision.

Ideal candidates have 8+ years in pharma DM, strong project management, and experience with eCRFs, EDC systems, and regulatory standards.

Qualifications

• 8+ years in Data Management in pharma/biotech or FDA-regulated env.
• Strong project management and multitasking ability.
• Familiarity with ICH/FDA, CDISC, GCDMP, 21 CFR 11, MedDRA, and drug dictionaries.

Responsibilities

• Lead data management tasks for phase 1–4 studies with minimal guidance.
• Represent DM on CTWG and mentor staff.
• Manage vendors/CROs and monitor progress.
• Design eCRFs and annotate CRF guidelines.
• Develop data edit checks, listings, and EDC testing plans.
• Contribute to Data Management SOPs and work instructions.
• Travel to off-site meetings or training as needed.

Skills

Lead studies

Vendor management

eCRF design

EDC testing

Data Mgmt plan

Regulatory standards

English communication

Travel readiness

Education

BA/BS in science

Tools

EDC systems

Data management tools

Job description

Parexel is hiring a Senior Clinical Data Manager in Mexico or Argentina.
The Senior Clinical Data Manager will be responsible for performing Data Management activities that support client’s commercial and development projects worldwide. He/she will participate as an active member of a multi-disciplinary team to plan, lead and execute the Data Management tasks required for phase 1-4 studies. The Senior Clinical Data Manager has a broad, fundamental knowledge of the data management process and is able to perform most required tasks with minimal guidance.

Essential Functions

• Be able to lead a large clinical study or a series of related studies with minimal guidance
• Represents Data Management on the CTWG for assigned studies
• Provide mentoring and training to lower level Data Management staff assigned to his/her studies
• Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies; build effective relationships with CRO / vendor counterparts
• Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design.
• Be able to perform a thoroughly detailed review of eCRF data requirements.
• Interact with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines.
• Lead the development of data edit check specifications and data listings
• Coordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards. Able to resolve EDC system issues with team members
• Develop or lead the development of the Data Management Plan for a clinical study.
• Able to review and provide feedback to the clinical team on other study documents e.g. Clinical Monitoring plans, Statistical analysis plans and vendor specifications
• May provide training on the EDC system and/or eCRF Completion Guidelines at Investigator Meetings and to internal and external study team members as needed
• Perform reconciliation of header data from external data sources against the clinical database
• Perform Serious Adverse Event reconciliation activities according to SOPs and guidelines
• Lead database upgrades/migrations including performing User Acceptance Testing
• Be able to maintain study workbooks and data management files
• Perform database lock and freeze activities per company SOPs
• Participate in regular team meetings and provide input when appropriate
• Provide input into the development of data management SOPs, Work Instructions, and process documents; take a leadership role in the development of assigned documents
• Contribute to a professional working environment including the application of client’s Code of Business Conduct and Ethics
• Assist with the training of new employees and/or contractors

Required Knowledge, Skills, and Abilities

• At least 8 years’ experience in Data Management for the pharmaceutical/biotechnology industry, or equivalent experience in an FDA-regulated environment, including study lead experience
• Has good project management skills and a proven ability to multitask
• Understands the scope and focus of Phase 1-4 clinical studies, and has a proven ability to perform most of the core Data Management tasks and interact with vendors.
• Possesses a comprehensive understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidances, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice.
• Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
• Possesses strong English language written and verbal communication skills.
• Experience and understanding of the Oncology or CNS therapeutic area, and with Phase III pivotal studies are preferred.
• Able to travel to off-site meetings or training seminars as needed.
• Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Prior experience with different Data Management systems and technologies, and Electronic Data Capture systems is desirable

Required/Preferred Education and Licenses

• BA/BS, preferably in the scientific/healthcare field.

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