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Clinical Project Manager - Patient Experience Data
Contract: North Chicago, Illinois, US span>
Salary Range: 40.00 - 45.00 | Per Hour
Job Code: 367855
End Date: 2026-03-29
Days Left: 28 days, 5 hours left
To Discuss more about this job opportunity, please reach out to Deepak Arya LinkedIn URL www.linkedin.com/in/deepak-arya-8a79aa22a/ , email your updated resume at Email deepak.arya@collabera.com. Thank you!
Pay Range: $60 to $65 an hour
Industry: Pharmaceutical
Work Type: 100% Remote
Contract Duration: 12 Months (Possibility of Extension)
Job Summary:
The Senior Manager, Patient Experience Data and Strategy will play a critical leadership role within the Patient Centered Outcomes Research function in a large enterprise environment. This position is responsible for independently designing and executing patient experience data strategies across oncology clinical development programs. The role focuses on optimizing product registration, access, and reimbursement through purposeful generation and analysis of patient centered outcomes data. The ideal candidate brings strong quantitative expertise, deep knowledge of psychometric methods, and the ability to translate complex analyses into impactful regulatory and scientific communications.
Key Responsibilities:
- Conduct literature and landscape reviews to develop disease conceptual models centered on patient focused outcomes within oncology programs.
- Identify and statistically evaluate existing clinical outcome assessment tools to determine fitness for purpose using rigorous quantitative methodologies.
- Lead the development, validation, and integration of clinical outcome assessment measurement strategies within clinical development programs, including protocol and statistical analysis plan content development.
- Design and execute patient experience data research using advanced quantitative methods such as factor analysis, reliability and validity testing, and statistical programming for endpoint analysis in clinical trials.
- Develop high level technical documentation to support regulatory and reimbursement submissions by translating complex quantitative findings into clear and actionable insights.
- Drive strategic scientific communication efforts including publication development and presentations at peer reviewed journals and medical congresses.
- Establish and promote best practices for quantitative patient experience data and clinical outcome assessment analysis across multifunctional teams.
- Manage publication processes to ensure statistical rigor, scientific integrity, and alignment with regulatory expectations.
Required Qualifications:
- Advanced degree such as MS, MPH, PharmD, or PhD in Biostatistics, Epidemiology, Health Economics and Outcomes Research, Public Health, or a related quantitative discipline.
- Minimum of 3 years of direct research experience with strong hands on quantitative and statistical analysis of clinical trial and patient reported outcome or clinical outcome assessment data.
- Deep understanding of measurement science principles and advanced psychometric and statistical methodologies applied in clinical research.
- Proven experience developing and implementing statistical analysis plans for clinical outcomes research.
- Strong ability to synthesize complex healthcare data into insights suitable for regulatory and cross functional stakeholders.
- Demonstrated experience collaborating within multifunctional teams in clinical or healthcare environments.
Preferred Qualifications:
- Experience in oncology clinical development programs.
- Experience supporting regulatory submissions involving clinical outcome assessment endpoints.
- Experience presenting data at scientific congresses and publishing in peer reviewed journals.
Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)
Job Requirement
- Biostatistics
- Psychometrics
- Clinical Trial Data Analysis
- PRO and COA Endpoints
- Statistical Analysis Plans
- Regulatory Submissions
- Oncology Research
Reach Out to a Recruiter
- Recruiter
- Phone
- Deepak Arya
- deepak.arya@collabera.com