Manager - Pearl River, United States - Pfizer

Pfizer

Verified Company

Pearl River, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.

Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

The primary responsibility of this position is to provide logístical support to clinical study teams for Vaccine Research and Development (VRD) clinical and research studies.

This includes providing training and data management support to clinical studies, study managers, clinical site operations, study team leads, and data management.

The colleague manages their own time to meet objectives; forecasts and plans resource requirements (people, financial, and technology) for projects within VRD.

Provides guidance to and/or may lead/co-lead moderately complex projects. Oversees direct reports and manages the growth and development of a team.

How You Will Achieve It

Manages and leads people and technological aspects within the Sample Logistics and Solutions (SLS) team as part of VRD.
Actively shares knowledge with others within SLS through existing knowledge sharing processes/systems.
SME on clinical trial sample collection and provides training to clinical sites. Interface with study teams to develop shipping schedules. Assist study managers with completing courier questionnaire and provide guidance to study managers on regional sample management requirements. Facilitate resolution of sample shipping issues including shipping supplies, couriers, customs, and permits.
Maintain and customize the clinical site training materials for each study and amendment, including training slides and detailed information contained in the site Study Reference Manual.
Provide support for queries and resolve issues from global study teams on the sample management process, including the process for sample collection, sample processing, storage, shipping, and logistics. Attends study team meetings on an ongoing basis to maintain awareness of any issues in the individual studies that may affect sample management and to address the issues proactively with the study teams.
Interface between clinical operations, study management, data management, and Clinical Immunology and Highthroughput Operations (CIHO) to ensure clear communication and issue resolution regarding sample data as well as testing data.
Work with clinical sites/partners to resolve sample/shipment discrepancies.
Identifies existing process/product improvements and may take appropriate risks to develop innovative ideas/processes/ products and advance new concepts that improve the department's work processes/products.
Recognizes others' need for development and collaborates with individuals to create a development plan.
Is accountable for general effective people management and development.
Manages the performance of direct reports through goal setting, ongoing assessment, and coaching.
Guides direct reports on relevant experiences to meet career objectives.
Qualifications

Must-Have

BS in a scientific discipline with 8 years of industry experience or
MS in a scientific discipline with 6 years of industry experience.
Previous supervisory experience is required.

Nice-to-Have- Excellent written and oral communication skills Excellent analytical abilities and problem-solving skills. Ability to provide leadership, set priorities and be accountable to timeline. Training in a GCLP/GLP/GMP environment and other international regulatory guidelinesNON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

This position may require occasional weekend and evening work to meet critical business timelines. This position may require travel to clinical sites, scientific meetings, or other business-related travel

Other Job Details:

Eligible for Employee Referral Bonus
Eligible for Relocation Assistance

Work Location Assignment:
On Premise

On Premise colleagues work in a Pfizer site because it's needed to get their job done. They may have flexibility to work remotely from time to time, but they are primarily on-site.

Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.

These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.

Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer o