Pfizer

SiteCarePartner(Manager)

Taiwan FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Site Care Partner (Manager) at Pfizer. Skills: project management, clinical studies management, resource planning. manage the clinical studies. planning, directing, creating and communicating timelines”

What You'll Achieve.

enable better health and treatment outcomes; Empower healthcare decisions regarding the safe and appropriate use of medicines for patients; achieve new milestones and help patients across the globe; meet objectives; achieve key milestones within time, cost and quality parameters

Industry & Context.

Problems you'll solve

problem solving ability

What They're Looking For.

Must Have

Bachelor's Degree, 7+ years’ experience in clinical trial field, Demonstrated project management / leadership experience, Experience working in the research and development of pharmaceutical industry, Experience conducting, managing or participating in regulatory inspection processes, Knowledge of project management discipline and its application to vaccine development, Country level cultural awareness and interpersonal skills, Excellent communication skills, both written and verbal in English

Nice to Have

Master's degree, Site Care Partner experience, Experience in early drug development, Knowledge of the project management discipline and its application to vaccine/drug development

What You'll Do.

manage the clinical studies

creating and communicating timelines

ensure that the clinical studies are within time

provide guidance to operational teams for managing projects

preparing forecasts for resource requirements

providing areas of improvement for products

processes or services

advancing new concepts and methodologies

facilitate agreements between different teams

Oversee the overall execution of clinical studies

development of realistic detailed study startup and monitoring plans

Oversee and support study start up activities at the country level

review of key documents

address regulatory and/or ethics committee questions

Forecast and manage the Clinical Trial Budget

Manage full studies for Operational Study Management or manage a unique part of a larger study

Serve as primary point of contact for study decisions related to the protocol

data collection and volunteer activities

Approve and oversee drug supply management

manage flow of drug supply to the sites

manage the program to achieve key milestones within time

cost and quality parameters

resolve or triage site level issues

Share and escalate plan deviations to Clinical Project Manager and study team

address Significant Quality Events or other quality issues at patient and/or site level

Lead the data integrity and data quality activities for assigned protocols

Provide regional and cross-regional insights on study-site performance and trends to / from the study team

How You'll Work.

Team & Collaboration

cross-functional coordination; facilitate agreements between different teams; Partner with key team members; Work with functional lines and directly with Contract Research Organization (CRO) line functions; Share and escalate plan deviations to Clinical Project Manager and study team; Provide regional and cross-regional insights on study-site performance and trends to / from the study team

Communication Scope

Excellent communication skills, both written and verbal in English

Process & Methodology

planning, directing, creating and communicating timelines, ensure that the clinical studies are within time, budget and scope, planning skills will help in preparing forecasts for resource requirements, Knowledge of project management discipline and its application to vaccine development, Demonstrated project management / leadership experience, manage own time to meet objectives and plan resource requirements for projects across the division, development of realistic detailed study startup and monitoring plans, manage the program to achieve key milestones within time, cost and quality parameters

Full Job Description

**Why Patients Need You** Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients. **What You Will Achieve** You will be part of Pfizer's medical team and manage the clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope. As a Manager, you provide guidance to operational teams for managing projects. Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement for products, processes or services. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams. It is your problem solving ability and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. **How You Will Achieve It** * Provide guidance, lead/co-lead projects, manage own time to meet objectives and plan resource requirements for projects across the division. * Oversee the overall execution of clinical studies and be accountable for the development of realistic detailed study startup and monitoring plans. * Oversee and support study start up activities at the country level, including review of key documents and providing support to address regulatory and/or ethics committee questions. Forecast and manage the Clinical Trial Budget. *

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