Patient Reported Outcomes Manager I
$50 - $59.52 per hourjob summary:
Join a top-tier global pharmaceutical leader driving patient-centric innovation in clinical trials. As a Patient Reported Outcomes (PRO) Manager I, you will oversee Clinical Outcome Assessments (COA) strategies and project management across multiple active clinical studies in a fast-paced environment. location: North Chicago, Illinois
job type: Contract
salary: $50.00 - 59.52 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
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 View email address on us.fitly.work.
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.
Join a top-tier global pharmaceutical leader driving patient-centric innovation in clinical trials. As a Patient Reported Outcomes (PRO) Manager I, you will oversee Clinical Outcome Assessments (COA) strategies and project management across multiple active clinical studies in a fast-paced environment. location: North Chicago, Illinois
job type: Contract
salary: $50.00 - 59.52 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Support clinical outcome assessment strategies and operational implementation across assigned protocols.
- Research study requirements, secure necessary COA licensing, and oversee vendor workflows for translations and localization.
- Manage timelines, deliverables, and cross-functional study priorities using Smartsheet.
- Lead cross-functional meetings to align teams, drive decision-making, and establish clear action items.
- Deliver day-to-day project management support to ensure seamless study execution.
qualifications:
- Foundational understanding of Clinical Outcome Assessments (COA) and Patient Reported Outcomes (PRO).
- Strong clinical trial study management or Project Manager (PM) experience.
- Proficiency with Smartsheet or equivalent project management tools.
- Exceptional organization, communication, and multi-tasking skills.
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 View email address on us.fitly.work.
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.
Vacancy posted 11 days ago
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