Senior Clinical Data Manager - FSP

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

​​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

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​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

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​Required/Preferred Education and Licenses

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