Senior Clinical Data Manager

We are seeking a Senior Clinical Data Manager for a Remote, contract position supporting a global leader in the eye health sector. This organization maintains an extensive international footprint, dedicated to enhancing vision through a diverse portfolio of pharmaceutical and surgical products that serve patients across nearly 100 countries. In this role, you will leverage advanced clinical data management technologies to drive data integrity and operational excellence within a large-scale research and development environment.

The standout feature of this opportunity is the level of autonomy and strategic leadership you’ll possess as you take full ownership of an entire therapeutic area’s clinical data strategy. We are searching for a proactive, visionary leader who excels at orchestrating the end-to-end data lifecycle—from initial CRF design to the final database lock—while mentoring a talented team to achieve operational excellence.

This role is a perfect launchpad for professional growth, offering you a masterclass in global vendor management and high-level decision-making within a complex regulatory landscape. You will thrive in a culture that genuinely values continuous learning and provides the flexibility of a fully remote environment, ensuring you achieve a true work-life balance while doing high-impact work. Join us to transform raw data into life-changing medical solutions, gaining invaluable experience in a supportive environment where your leadership is the cornerstone of our success.

Contract Duration: 12 months to start

• 3 years + DM experience
• 4+ years of industry experience
• Bachelors Degree in a related field such as Sciences and/or Health Sciences
• Ophthalmology Study experience
• Experience in CRF Design/EDC
• Ability to facilitate and manage operational activities that have been contracted out to third party vendors (such as CRO's, Labs).
• Strong understanding of regulatory requirements and guidelines. Ability to work on a multi-disciplinary team and to contribute across multiple projects with competing priorities.
• Demonstrated project management skills including pro-active project planning.
• Demonstrated leadership, decision-making ability, organizational skills and excellent verbal and written communications ability.
• Strong analytical and problem-solving skills
• Broad interpersonal skills to interact with all levels of internal and external customers are necessary

• EDC experience preferably with Zelta

Under the supervision of the Senior Director/Director, Data Management, this position is responsible for managing all data management projects in a therapeutic area. This position will supervise subordinate data management personnel. This involves exercising sound data management judgments within broadly defined regulations and internal procedures to achieve high quality and accurate clinical data. This position represents the Data Management group on multiple project teams in the responsible therapeutic area.

Closely interact with all levels of managements, internally and externally, to address any clinical data management related issues. Ensure data management project timelines are met.

• Manage all study specific data management activities such as CRF design, CRF flow definition, DMP preparation, database setup and validation, data entry, data review, discrepancy management, CRF/DCF tracking, data reporting, data coding, database lock, project documentation, transfer to biostatistics for analysis, electronic submission and archiving.
• Manage external contractors, laboratories and contract research organizations on data management activities.
• Ensure SOP and guidelines related to data management are followed and maintained.
• Maintain data management project documentation and overall responsibility for its content.
• Responsible for sign-off on the final locked database delivered for analysis.
• Represent Data Management group on the project team meetings and timeline discussions.
• Support internal as well as vendor audits to ensure compliance with SOP.