Clinical Research Associate

Globus Medical develops innovations to improve the quality of life of patients with musculoskeletal disorders and improve surgical techniques and outcomes. The Clinical Research Associate monitors and supports clinical study sites, ensuring participant safety, clinical data integrity, protocol compliance, and regulatory adherence. The role serves as a liaison between the sponsor and investigational sites and collaborates with cross-functional teams to support successful clinical research execution.

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

Preferred

Familiarity with FDA regulations, ISO 14155, EU MDR requirements, and/or other applicable clinical research regulations preferred

Proficiency with Microsoft Office applications

experience with electronic data capture (EDC), clinical trial management systems (CTMS), or other clinical research technologies preferred

FDA Regulations

ISO 14155

EU MDR Requirements

Clinical Research Regulations

Microsoft Office

Electronic Data Capture (EDC)

Clinical Trial Management Systems (CTMS)

Clinical Research Technologies

Company

Musculoskeletal device manufacturer and distributor

Audubon, Pennsylvania, USA

http://www.globusmedical.com/

Founded in 2003

1001-5000 employees

Qualifications

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

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

Familiarity with FDA regulations, ISO 14155, EU MDR requirements, and/or other applicable clinical research regulations preferred

Proficiency with Microsoft Office applications

Experience with electronic data capture (EDC), clinical trial management systems (CTMS), or other clinical research technologies preferred

Minimum of 1-3 years of experience in clinical research within the medical device, biotechnology, or pharmaceutical industry, including direct experience monitoring clinical studies.

Required skills

Clinical Research Monitoring, Clinical Practice (GCP), FDA Regulations, ISO 14155, EU MDR, Microsoft Office, Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS)

Preferred skills

Proficiency with Microsoft Office applications, Glassdoor, 2.6, Audubon, Pennsylvania, USA, http://www.globusmedical.com, H1B Sponsorship, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, 67, Represents job field similar to this job, Engineering and Development, Legal and Compliance, Management and Executive, Product Management, Customer Service and Support, Arts and Entertainment, Accounting and Finance, Trends of Total Sponsorships, *2026, (25), 2025, (24), 2024, (17), 2023, (13), 2022, (8), 2021, (9)

Experience

1-3 years