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: $40 to $45 an hour. 

Industry: Pharmaceutical

Contract Duration: 12 Months (Possibility of Extension)

Job Summary:
The Patient Reported Outcomes PRO Manager is responsible for driving and managing PRO and ePRO activities during clinical trial start up. This role ensures timely execution of licensing translation and implementation processes to support study timelines and minimize delays. The position acts as a central point of coordination across cross functional teams vendors and stakeholders. The associate provides subject matter expertise in patient centered outcomes to improve operational efficiency and compliance. This role operates within a global clinical research environment and supports program delivery through strong project execution.

Key Responsibilities:

• Manage PRO and ePRO processes from licensing through study start up ensuring timely execution of deliverables.
• Coordinate with PRO owners vendors and internal stakeholders to support implementation activities.
• Oversee translation licensing agreements and vendor related activities aligned with study timelines.
• Track project milestones timelines and deliverables to prevent delays in clinical trials.
• Maintain documentation repositories and ensure accurate record keeping for PRO related assets.
• Provide guidance and training to internal teams on PRO and ePRO processes.
• Collaborate with cross functional teams including clinical data and research groups to ensure alignment.
• Ensure adherence to regulatory requirements standard operating procedures and global clinical practices.

Required Qualifications:

• Bachelor degree in a scientific field or equivalent relevant experience
• Minimum 4 years of clinical research or project management experience
• At least 1 year of hands on experience with Patient Reported Outcomes or outcomes research
• Strong project management skills with ability to manage timelines and deliverables
• Knowledge of Good Clinical Practice and standard operating procedures
• Strong communication and stakeholder management skills

Preferred Qualifications:

• Experience with ePRO systems and electronic data capture tools
• Background in health economics and outcomes research
• Experience working in global clinical trial environments
• Familiarity with vendor management and outsourcing processes
• Experience supporting study start up activities

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)