Sr. Field Clinical Research Associate

Medasource; United States; Remote; USD 80,000 - 110,000; Part time

Job summary

A leading company in the life sciences sector is seeking a Sr. Clinical Research Associate for a 12-month contract role. This remote position requires travel in Upstate NY and involves monitoring clinical studies, ensuring compliance, and collaborating with various teams. Ideal candidates will have a Bachelor's degree in a related field and at least five years of clinical research experience.

Qualifications

• At least five years of clinical research experience.
• Ability to interpret clinical data and work independently within a global team.
• Proficiency in word processing.

Responsibilities

• Monitor clinical studies for compliance with regulatory requirements.
• Coordinate with study teams to enroll sites and subjects.
• Train site personnel on protocol and regulations.

Skills

Communication

Interpersonal Skills

Analytical Skills

Organizational Skills

Education

Bachelor’s degree in natural sciences, pre-medicine, nursing, bioengineering, or related field

Tools

Clinical applications

Job description

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Job Title: Sr. Clinical Research Associate

Location: Remote with Travel required in Upstate NY

Client: Large Life Sciences Company

Duration: 12 month contract with the possibility for extension

Job Duties:

• Monitor clinical studies at sites in an assigned territory to ensure compliance with regulatory requirements, GCP, and accuracy standards, including site initiation, periodic, and close-out visits.
• Ensure regulatory and protocol compliance for all assigned projects, including reviewing data, reporting adverse events and protocol deviations, and reporting device complaints and malfunctions.
• Coordinate with study teams and specialists to enroll sites and subjects, facilitate data queries, and resolve issues.
• Report monitoring findings promptly according to SJM processes.
• Collaborate with teams to submit study documents and participate in training sessions.
• Train site personnel on protocol and regulations; mentor less experienced team members as needed.
• Maintain high communication standards with internal and external stakeholders.

Minimum Qualifications:

• Bachelor’s degree in natural sciences, pre-medicine, nursing, bioengineering, or related field.
• At least five years of clinical research experience.
• Strong communication, interpersonal, analytical, and organizational skills.
• Ability to interpret clinical data and work independently within a global team.
• Proficiency in word processing and clinical applications.

Preferred Qualifications:

• Prior clinical monitoring experience.
• Familiarity with cardiac, vascular, or neuromodulation technologies.
• Experience in medical device/pharmaceutical companies or clinical/hospital settings.
• Industry certification (e.g., SoCRA, ACRP).

Seniority level

• Associate

Employment type

• Part-time

Job function

• Research, Science, and Project Management

Industries

• Pharmaceutical Manufacturing, Biotechnology Research, Medical Equipment Manufacturing