Clinical Research Associate

Globus Medical•Audubon, PA

6d•Hybrid

About The Position

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible. Position Summary: The Clinical Research Associate (CRA) is responsible for monitoring and supporting clinical study sites to ensure the rights, safety, and well-being of study participants and the integrity of clinical data. The CRA conducts site qualification, initiation, interim monitoring, and closeout activities in accordance with study protocols, applicable regulations, Good Clinical Practice (GCP), and company standard operating procedures (SOPs). The CRA serves as a primary liaison between the sponsor and investigational sites, providing guidance on protocol requirements, regulatory compliance, data collection, and study conduct. Responsibilities include reviewing study documentation, verifying source data, identifying and resolving site issues, and ensuring timely and accurate reporting of study data and adverse events. The CRA maintains current knowledge of clinical research regulations, industry standards, and therapeutic area developments. The position may contribute to the development and review of study-related materials, including informed consent forms, case report forms, source documents, site training materials, and monitoring plans. The CRA collaborates with cross-functional teams to support study objectives, maintain data quality, and ensure successful execution of clinical research projects.

Requirements

Excellent verbal, written, and interpersonal communication skills, with a demonstrated ability to collaborate effectively across functions and contribute to a positive, team-oriented culture.
Bachelor's degree in a scientific, healthcare, engineering, or related discipline; equivalent combination of education and relevant clinical research experience may be considered.
Minimum of 1-3 years of experience in clinical research within the medical device, biotechnology, or pharmaceutical industry, including direct experience monitoring clinical studies.
Working knowledge of clinical research principles, Good Clinical Practice (GCP), and applicable regulations governing clinical studies.
Familiarity with FDA regulations, ISO 14155, EU MDR requirements, and/or other applicable clinical research regulations preferred.
Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities, meet deadlines, and maintain attention to detail in a fast-paced environment.
Proficiency with Microsoft Office applications; experience with electronic data capture (EDC), clinical trial management systems (CTMS), or other clinical research technologies preferred.
Ability to travel up to 70% of the time

Responsibilities

Conducts remote and on-site monitoring activities, including site qualification visits, site initiation visits, interim monitoring visits, and closeout visits, in compliance with standard operating procedures and applicable regulatory requirements.
Develops monitoring expertise through ongoing training and collaboration with senior clinical team members.
Reviews source documentation, verifies study data, evaluates protocol compliance, and ensures timely identification, documentation, and escalation of study issues, including adverse events, protocol deviations, and corrective and preventive actions.
Monitors site enrollment, retention, protocol compliance, and data quality metrics; identifies site performance issues and collaborates with investigators, site personnel, and study leadership to support timely resolution.
Supports site compliance with study protocols, Good Clinical Practice (GCP), applicable regulations, company procedures, and sponsor requirements through routine monitoring, issue identification, and follow-up activities.
Establishes and maintains productive working relationships with investigators, site personnel, sales representatives, and internal stakeholders to support study execution, evaluate site feasibility, and promote successful study outcomes.
Supports the development, review, and maintenance of study documents for assigned studies, including clinical study protocols, case report forms and subject questionnaires, informed consent forms, electronic data capture (EDC) systems, and other study tools.
Participates in process improvement initiatives and contributes feedback to support the enhancement of clinical operations procedures, tools, templates, and best practices.
Contributes to a highly collaborative and solutions-oriented team culture by actively participating in study team meetings, sharing site-level updates and insights, and supporting cross-functional initiatives.
Demonstrates a positive attitude, adaptability, and a willingness to contribute to departmental projects and organizational priorities as needed.
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies.
Ensures compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to the role.
Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties.
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.