Contract CRA: Site Activation & Compliance

Medasource; Maple Grove (MN); On-site; USD 55,000 - 96,000; Part time

Job summary

Medasource is seeking a Clinical Trial Support professional to participate in Abbott clinical studies, ensuring site activation and compliance with study protocols. You will work with Abbott staff and internal teams to coordinate start-up, maintenance and close-out of study sites, review essential regulatory documents, and support data review and issue resolution.

The role requires a Bachelor’s degree in a natural science or healthcare field, strong communication skills, and proficiency in

Qualifications

• Bachelor's degree or equivalent with focus in natural science or healthcare fields.
• Strong written and verbal communication, interpersonal and analytical skills.
• Proficiency in Microsoft Office; ability to interpret basic clinical data and meet deadlines.

Responsibilities

• Assist in regulatory and protocol compliance for clinical projects at assigned sites.
• Coordinate start-up, maintenance and close-out of study sites with Abbott staff and internal teams.
• Review informed consent documents for required elements.
• Analyze study data and regulatory documents for accuracy.

Skills

Communication

Interpersonal skills

Analytical skills

Organizational skills

Presentation skills

Microsoft Office

Education

Bachelor's degree in natural science / pre-medicine / nursing / bioengineering

Tools

Microsoft Office Suite

Job description

Medasource is seeking a Clinical Trial Support professional to participate in Abbott clinical studies, ensuring site activation and compliance with study protocols. You will work with Abbott staff and internal teams to coordinate start-up, maintenance and close-out of study sites, review essential regulatory documents, and support data review and issue resolution.

The role requires a Bachelor’s degree in a natural science or healthcare field, strong communication skills, and proficiency in