This is a hybrid position that requires onsite work 2-3 days a week, based on the team requirements. Remote work/high travel to site is not an option. Employees must be within a commutable distance of the job location. Relocation packages are available to qualified hires.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
The Senior Clinical Research Associate (SCRA) conducts in-house and external monitoring to verify that reported data collected in Clinical Lab Studies and Field Trials are accurate, complete, and verifiable from source documents and to ensure that the studies are conducted in compliance with the current approved protocol, GCP/ VICH requirements, FDA/CVM Regulations, and BI SOPs. The SCRA is responsible for ensuring quality of study protocols, raw data, and reports to support registrations and other claims related to veterinary products.
The SCRA performs these duties for on-site and off-site (national and global) clinical studies and trials for all animal species and across all product modalities. Duties include interaction with CROs/Investigators, monitoring of study status, quality control and integrity of data, management of study data and procedures in compliance to GxP and relevant regulatory guidelines. The SCRA drafts protocols and reports and can act as a Study Leader for studies. The SCRA is responsible for tracking timelines and deliverables and interfacing with internal collaborators (e.g., clinical trial supply, data management, regulatory affairs, PV). The SCRA acts as a trainer, mentor, and resource to CRAs and Study Coordinators and acts as an expert in data and documentation quality.