Oversight CRA

Randstad USA; Chicago (IL); On-site; USD 96,000 - 124,000; Full time

Job summary

Randstad USA is seeking an Oversight Clinical Research Associate on a 6-month contract located in Chicago, Illinois. The CRA will oversee clinical research at investigational sites to ensure compliance with study protocols, site monitoring plan, regulatory standards, IRB/EC policies, and Sponsor requirements.

This role works under minimal supervision with Sponsor/CRO study teams and site personnel to resolve site issues.

Qualifications

• 5+ years of onsite clinical monitoring experience with proficiency in GCP.
• Bachelor's Degree or equivalent (scientific or healthcare discipline preferred).
• Strong experience in pain/post-op pain clinical trials.

Responsibilities

• Conducts quality oversight and CRA evaluation visits to ensure adherence to SOPs, monitoring plan, and regulatory standards.
• Performs training and shadowing visits as a senior monitor to coach CRAs.
• Performs site monitoring visits or oversees monitoring visits conducted by CRA.

Skills

Site Monitoring

GCP

Education

Bachelor's Degree

Job description

Job Summary

6-month contract for Oversight CRA located in the Southeast U.S. The Oversight Clinical Research Associate is responsible for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, site monitoring plan, applicable regulatory standards, IRB/EC policies and procedures and Business requirements. This position works under minimal supervision, working closely with the Sponsor/CRO study teams and site personnel for resolution of site issues.

Location & Details

location: Chicago, Illinois

job type: Contract

salary: $70 - 90 per hour

work hours: 9 to 5

education: Bachelors

Responsibilities

• Conducts quality oversight and CRA evaluation visits to ensure site and CRA adherence to the study Monitoring Plan, Standard Operating Procedures, the Clinical Investigational Plan, Monitoring Plan, applicable regulatory, IRB/EC, and Sponsor standards, guidelines and policies
• Conducts training and shadowing visits as a senior monitor to coach, mentor, and verify quality of CRAs.
• Performs site monitoring visits or oversees monitoring visits conducted by CRA

Qualifications

• 5+ years of onsite clinical monitoring experience and an understanding and proficiency in GCP
• Bachelor's Degree or equivalent (scientific or healthcare discipline preferred)
• Strong experience in pain/post-op pain clinical trials required

skills: Site Monitoring, Good Clinical Practice (GCP)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.