yst Patient Oriented Programs
yst Patient Oriented Programs
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Job Description
Summary
The primary responsibility of this role is to manage patient oriented program (POP). Responsible to ensure compliance in POP end to end activities as per the applicable process and quality standards. Liaison with the cross functional team for successful of POP.
About The Role
yst PatientOriented Program
Location Hyderabad Hybrid
About The Role:
The primary responsibility of this role is to manage patient oriented program (POP). Responsible to ensure compliance in POP end to end activities as per the applicable process and quality standards. Liaison with the cross functional team for successful of POP.
Key Responsibilities:
- Administer end to end POP process on behalf of Business Owner (BO) in accordance with Doing Business Ethically (DBE) policy and POP Standard Operating Procedures (SOP).
- Coordinate with all POP stakeholders (POP Champion/ Procurement/ Legal/ Patient Safety/ Compliance/Quality urance) and create POP doents.
- Responsible for obtaining the necessary approvals for conduct of POP in a timely manner. Responsible for the overall management of the External Service Providers (ESP) compliance check prior to fieldwork initiation.
- Enter program details in the POPsys database throughout the conduct of the POP. Keep track of all required activities (First Participant First Contact (FPFC)/Last Participant Last Contact (LPLC) dates Adverse Event Reconciliation (AER) Periodic Reviews closure etc.) related to POP conduct and ensure no monitoring gaps before program closure in POPsys.
- Maintain doentation for all POP related activities in POP repository. Ensure identified quality issues are well doented in quality issue (QI) management tool. Create issue record and perform proper investigation root cause ysis followed by risk essment and corrective and preventive actions (CAPA).
- Ensure proper handover of activities when leaving the role/organization/planned leaves and liaise with POP Champion. Effective management of all projects igned and timely escalation of findings related to projects. Seek constant feedback from stakeholders and improve on suggestions put forth.
Essential Requirements:
- Preferrable experience with 2 5 years experience in the pharmaceutical industry within Clinical Pharmacovigilance (PV) Medical/regulatory Affairs or relevant experience in pharma compliance or commercial framework.
- Good understanding of local regulatory requirements and applicable policies surrounding pharmaceutical industry
- Ability to communicate effectively across different audiences organizational levels and local and global teams.
Desirable Requirements:
- College/university degree preferably in security criminal justice crisis management business continuity or other related field. Advanced degree is highly desirable (e.g. Masters degree or MBA).
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Remote Work :
No
Employment Type
Full Time
