Associate Manager, Clinical Research Program
Stryker is hiring an Associate Manager, Clinical Research Program to lead end-to-end clinical trial management — from planning through execution to closure. In this role, you’ll collaborate with cross-functional teams and Contract Research Organizations to generate high-quality clinical evidence that supports patient access to advanced venous thromboembolism care
What You Will Do:
• Lead the development and implementation of global clinical trial strategies aligned with business objectives.
• Define study objectives, scope, timelines, and resource needs.
• Develop essential study documentation, including Clinical Investigation Plans, Investigator Brochures, Safety Plans, and Data Management Plans.
• Provide clinical training to investigators, site staff, CRO partners, and internal teams.
• Oversee data evaluation and validation throughout the study lifecycle; contribute to publications and reports.
• Ensure sponsor oversight of clinical sites and CROs to maintain compliance with protocols and objectives.
• Participate in CRO selection and management, conduct site visits and support publication initiatives.
• Engage key physician investigators and thought leaders in clinical research efforts.
• Collaborate cross-functionally to support regulatory submissions, reimbursement, and market expansion.
• Maintain current knowledge of scientific and clinical developments through literature review, conferences, and expert interaction.
• Develops and manages study budgets and provide regular updates to leadership.
• Promote adherence to clinical SOPs and continuously improve study processes and quality.
What You Need:
Required:
• Bachelor’s degree in a scientific, health-related, engineering, or other relevant field required.
• 6+ years’ relevant clinical research experience
• Project management experience.
Preferred:
• Master’s degree preferred.
• Experience with Good Laboratory Practice (GLP) and Good Clinical Practice (GCP)
• Solid understanding of industry trends for clinical and regulatory pathways
• Medical device trials experience preferred.
• Detail oriented with ability to deliver high quality output consistently and on time.
• Ability to thrive in times of change while adhering to cultural focus on People and Patients.
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