Contribute to trial synopsis, protocol, and amendments to ensure operational feasibility; contribute to defining the Case Report Form content; develop study-specific procedures, contribute to the monitoring plan and other operational documents.
Contribute to system testing as required (e.g. UAT for eCRF screens, database structure, data loading). Ensure proper collection and validation of data and documentation in a timely manner.
Communicate to teams regarding monitoring activities, data flow, and data validation / cleaning; perform patient data validation homogeneously and fulfill required quality standard; ensure study documentation is properly maintained and archived in the Trial Master File
Coordinate and support field-monitoring activities; maintain monthly study highlights (including enrollment curves and timelines) in a timely manner.
Work with trial project teams to assess project risks and issues.
Understand project deliverables and achievement of deliverables.
Communicate with team on changes in project, policy, and priorities.
Responsible to work with health registries and large databases
Work in compliance with clinical process, regulations and data management
Ability to work independently on multiple projects with ability to prioritize tasks
Responsible for initiating and managing research contracts for Investigator Initiated Studies (if applicable)
Support the development and execution of strategies to obtain information and support concerning medical devices undergoing clinical investigation, post market surveillance or marketed/product use evaluation
Responsible for driving study results to be published in peer-reviewed journals
Manage ongoing Investigator-Initiated Studies and/or Stryker Initiated Studies (as applicable)
Set and manage deliverables for contracts to align with research strategy
Develop and maintain overall dashboard of clinical and non-clinical studies, including major milestones, objectives, and financial aspects.
Support pre-clinical studies and develop non-clinical studies protocols to support existing products or investigate new products with cross functional support (if applicable)
Work with internal and external resources to facilitate publication of study results in peer-reviewed journals. •
Partner with Legal and Finance team to ensure researchers are reimbursed in compliance with their contracts.
Presents study results/updates to various internal stakeholders cross functionally, as needed.
Work with clinicians, on-site research assistants, and Stryker teams to generate protocols that provide necessary information for publications, presentations or technical monographs.
Evaluate quality of work for a variety of job roles and specialized functions; evaluate workload, quality and budget metrics through regular review and reporting of findings; collaborate with senior management and other functional leadership to improve efficiencies, project outcomes and quality metrics for clinical projects.
Evaluate quality of work for a variety of job roles and specialized functions; evaluate workload, quality and budget metrics through regular review and reporting of findings; collaborate with senior management and other functional leadership to improve efficiencies, project outcomes and quality metrics for clinical projects.
Lead or participate in departmental process improvement initiatives.
Bachelor’s degree in science or health care field required
Advanced degree (MSc, PhD) in biomedical engineering, sciences, health outcomes research, or related field preferred.
7+ years of related clinical research experience, preferably in clinical study management
Demonstrated understanding of laws, regulations, standards, and guidance governing the conduct of clinical studies, as well as preparation of clinical documentation in support of regulatory submissions.
Demonstrated interpersonal, written, and oral communication skills as well as excellent organizational and project management skills in a fast-paced environment.