Remote Field Clinical Research Associate - Part-Time Contract

Medasource; Chicago (IL); On-site; USD 40,000 - 80,000; Part time

Job summary

Medasource is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month contract focused on the North Central Region. You will monitor site performance, ensure compliance with GCP, and support study initiation and close-out visits.

The role requires strong experience in cardiac, vascular, or neuromodulation technologies, collaboration with cross-functional teams, and mentoring junior staff while delivering timely data and documentation.

Qualifications

• Minimum five years of clinical research experience with a broad understanding of all aspects of clinical research.
• Bachelor’s degree from an accredited university or college, preferably in natural science, pre-medicine, nursing, bioengineering, or a related field.
• Strong written, verbal, interpersonal, presentation, analytical, and organizational skills.
• Ability to interpret basic clinical data, meet deadlines, and communicate effectively with all levels of employees.
• Proficiency with word processing software and relevant clinical applications.
• Ability to work independently and within a dynamic, global team environment.
• Familiarity with cardiac, vascular, and/or neuromodulation technologies.
• Certification by an industry-recognized professional society (e.g., SoCRA, ACRP) or accredited institution (preferred).
• Experience in a medical device/pharmaceutical company or clinical/hospital environment (preferred).

Responsibilities

• Monitor clinical studies at sites in your assigned territory to ensure compliance with regulatory requirements, GCP, and study protocols, including site initiation, periodic, and close-out visits.
• Ensure regulatory and clinical protocol compliance for all assigned projects.
• Review data and source documentation from investigational sites for accuracy and completeness.
• Ensure timely and accurate reporting of adverse events, protocol deviations, device complaints, and malfunctions.
• Resolve site issues, identify root causes, and implement corrective actions.
• Coordinate with study teams, field clinical engineers, and specialists to enroll sites into new and ongoing studies.
• Facilitate enrollment of study subjects via site coordinators and resolve data queries.
• Report findings of monitoring visits promptly according to processes.
• Collaborate with in-house teams to ensure timely submission of study documents.
• Participate in conference calls and training sessions as required.
• Train site personnel to ensure compliance with study protocols and local regulations.
• Mentor less experienced clinical team members as requested.
• Demonstrate strong written and verbal communication with internal and external customers.

Skills

Clinical research experience

Communication skills

Analytical skills

Organizational skills

Mentoring junior team members

Education

Bachelor's degree in natural science/related field

Job description

Medasource is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month contract focused on the North Central Region. You will monitor site performance, ensure compliance with GCP, and support study initiation and close-out visits.

The role requires strong experience in cardiac, vascular, or neuromodulation technologies, collaboration with cross-functional teams, and mentoring junior staff while delivering timely data and documentation.