Senior Clinical Research Associate - Remote

Overview

MCRA, an IQVIA Business is seeking a Senior Clinical Research Associate to be a critical member of the clinical operations team, responsible for management of assigned investigator sites and all monitoring activities for assigned studies.

In Short

• Join a leading medical device advisory firm and clinical research organization.
• Manage assigned investigator sites and monitoring activities.
• Execute clinical affairs duties in accordance with GCP guidelines.
• Ensure compliance with Standard Operating Procedures (SOPs).
• Work with a team focused on regulatory, clinical research, reimbursement, and quality assurance.
• Contribute to the commercialization process from concept to market.
• Engage with a diverse range of therapeutic areas including orthopedics and neurology.
• Be part of a global presence with offices in the US, Japan, and Europe.
• Support over 1500 clients globally.
• Work in a dynamic and market-leading environment.

Requirements

• Experience in clinical research and site management.
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Strong organizational and communication skills.
• Ability to work independently and as part of a team.
• Detail-oriented with strong problem-solving skills.
• Experience in monitoring clinical trials.
• Familiarity with Standard Operating Procedures (SOPs).
• Ability to manage multiple projects simultaneously.
• Relevant educational background in life sciences or related field.
• Willingness to travel as required for site visits.

Benefits

• Competitive salary and benefits package.
• Opportunities for professional development and growth.
• Work in a collaborative and innovative environment.
• Engage with a diverse range of projects and clients.
• Access to industry-leading training and resources.
• Flexible work arrangements.
• Supportive team culture.
• Health and wellness programs.
• Retirement savings plan.
• Paid time off and holidays.