Lead Clinical Research Coordinator

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strategy clinical trial design and execution market access and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.

Overview

The Lead Clinical Research Coordinator plays a critical role in supporting the execution of clinical research studies by coordinating and performing remote clinical activities in compliance with study protocols Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP). This role is responsible for performing a variety of clinical procedures to collect record report and interpret patient data for individuals enrolled in or seeking enrollment in clinical studies.

Responsibilities and Duties

• Adhere to SOPs and Manual of Procedureswhen conducting all study-related activities to ensure compliance and consistency. This includes maintaining a working knowledge of study-specific software applications and equipment.
• Collaborate with the research team and study sites to identify recruit and virtually enroll eligible patients for clinical trials.
• Collect maintain and securely storeall relevant data associated with clinical research trials in accordance with regulatory and organizational standards.
• Educate potential participantsabout clinical research trials including study requirements and manage the informed consent process through virtual interactions.
• Assist with participant study complianceby providing guidance and reminders to ensure adherence to protocol requirements.
• Conduct follow-up activitiesfor clinical trials while maintaining adherence to Good Clinical Practice (GCP) guidelines.
• Ensure patient safetyby monitoring participants reporting adverse events promptly and ensuring compliance with IRB-approved protocols.
• Support the research participant call centeras assigned handling inquiries and providing assistance.
• Maintain professionalismin all interactions with research participants to foster trust and engagement.
• Assist with study equipment management and reporting ensuring proper tracking functionality and documentation.
• Communicate effectivelywith MCRA clinical affairs staff and clients providing updates and support under the guidance of senior MCRA staff as needed.
• Perform additional duties and projectsas assigned to support the success of clinical research operations.

Required Knowledge Skills and Experience

• Education: Bachelors degree required (preferably in a life sciences or healthcare-related field)
• Experience: Minimum of three years of experience as a Clinical Coordinator or in a comparable clinical research role
• Strong attention to detail
• Excellent verbal and written communication skills

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role when annualized is $49200.00 - $123000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.

Required Experience:

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