Clinical Affairs Internship: Dive into Clinical Research

Regulatory Toolkit; Mahwah (NJ); Sur place; USD 28 000 - 48 000; Plein temps

Avantages offerts par ce poste

Sign-on bonus

11 paid holidays

Corporate housing or living stipend

Résumé du poste

Stryker is offering a Clinical Affairs internship onsite in Mahwah, New Jersey. You will collaborate with R&D, Project Management, and Regulatory Affairs to support clinical research programs and gain exposure to senior leaders.

Responsibilities include literature reviews, clinical intelligence, and monitoring data with Clinical Research Associates, with opportunities to present findings and contribute to patient-centered projects.

Qualifications

• Pursuing a Bachelor’s or Master’s degree and must remain enrolled.
• GPA 3.0 or above (verified at hire).
• Must be legally authorized to work in the U.S. without sponsorship now or in the future.
• Strong written and verbal communication, collaboration and relationship-building.
• Proficiency in Microsoft Office and eagerness to learn in a dynamic environment.

Responsabilités

• Work cross-functionally with R&D Engineering, Project Management, Health Care Solutions, Marketing, and Regulatory Affairs to assist in clinical research programs.
• Perform clinical intelligence activities to understand treatment options and clinical studies.
• Accompany a Clinical Research Associate to monitor data at investigative sites.
• Prepare literature review summaries for evaluation of current clinical outcomes.
• Shadow CRAs at cross-functional team meetings to learn the collaborative development process.

Connaissances

Communication

Leadership

Problem-solving

Organizational skills

Microsoft Office

Formation

Bachelor’s or Master’s degree

Outils

Microsoft Office

Description du poste

Stryker is offering a Clinical Affairs internship onsite in Mahwah, New Jersey. You will collaborate with R&D, Project Management, and Regulatory Affairs to support clinical research programs and gain exposure to senior leaders.

Responsibilities include literature reviews, clinical intelligence, and monitoring data with Clinical Research Associates, with opportunities to present findings and contribute to patient-centered projects.