Pfizer

Senior Associate CSR

Reposted 5 Days Ago

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Makati City, Metro Manila, National Capital Region

Hybrid

Senior level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

The Senior Associate CSR manages the lifecycle development of Clinical Study Reports to support drug registration and approval, overseeing coordination, quality control, project management, and cross-departmental collaboration.

Summary Generated by Built In

This team ensures Pfizer's Clinical Study Report (CSR) management meets global agency standards and manages regulatory reporting, dossier development, and submission activities for Global Regulatory & International Operations (RIO). Members in the team oversee and manage end-to-end lifecycle development of CSR to support Pfizer's global drug registration and approval processes, including submission, publishing, and archiving of related reports and documents.

Lead the coordination, compilation, quality control, approval and post-approval processes associated with development of Pfizer global CSRs

Create CSR mockups in System and populate document templates

Project manage CSR compilation, approval and publishing activities

Execute submission ready Quality Control ( QC ) on CSR components and structure

Communicate with function lines regarding issues with CSR components and seek resolutions

Seek approval from signatories on finalized CSRs and update clinical trial registry with CSR milestone status

Prepare investigators declaration packages for distribution to the coordinating investigator

Prepare study data packages required for distribution to study Principal Investigator s ( PIs )

Coordinate Public Disclosure Synopsis ( PDS ) and Plain Language Summary ( PLS ) activities

Publishes the approved report into Pfizer standard submission-ready and regulatory compliant package, and contributes to submission package

Files the report to Trial Master Files (TMF) system to meet regulatory requirements

Monitor public mailbox

Provide ongoing quality reviews and process improvement suggestions to the work group or project team, supporting continuous enhancement of CSR coordination practices

Senior Associate (cumulative from above)

Serve as the subject matter expert for specific CSR coordination business areas, authoring and maintaining local Clinical And Medical Controlled Document (CMCD) / Standard Operating Procedure ( SOP ) /QC checklists, and managing document and email templates

Act as the system business administrator and primary point of contact for related processes

Independently leads moderately complex CSR projects and process improvement initiatives, providing guidance and mentorship to newly appointed CSR Coordinators where appropriate

Facilitate cross-departmental collaboration to streamline workflows, build consensus, and implement optimized CSR processes, regularly taking informal leadership roles to drive group agreements and progress.

Ensure proper workload distribution by factoring in team capacity and capability, while managing personal time to meet objectives for departmental projects

Provide ongoing quality reviews and process improvement suggestions to the work group or project team, supporting continuous enhancement of CSR coordination practices

maintain compliance and uninterrupted operations

Build the bridge across internal and external stakeholders to share CSR related regulations ( e.g. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use ( ICH ) E3), and be the leading voice of the team

Skill Requirements:

In-depth knowledge of drug development process
Independent delivery of all phases CSR for all Theraputic Areas (TAs) and advanced CSRs
Great CSR timeline management capability and decent CSR coordination communication skills
Demonstrated coordination of activities in a highly regulated environment and mastery of concurrent task management
Demonstrate an understanding of applicable filing regulatory guidelines and fluency regarding order and presentation of regulatory dossiers
In depth knowledge of regulatory guidance, data standards, and practices pertaining to technological aspects of submission management and publishing
Experience of successfully mentoring others
Demonstration of experience working in a customer service environment
Preferred skills in electronic submissions builds and/or publishing within the Pharmaceutical Industry
Preferred ability to troubleshoot independently and resolve technical issues efficiently

QUALIFICATIONS

Master's or bachelor's degree in biological, medical, pharmaceutical sciences or life sciences preferred
Proficiency in English and Chinese language preferred (read, written and spoken)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.