1,000+ matching jobs for “Associate Product Operations”

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Marathon Petroleum

Associate Business Analyst

Findlay, Ohio, United States

… steward of commercial master data and associated governance processes that support critical business operations across the enterprise. This role is responsible for ensuring the accuracy, integrity, consistency, and …

Added Oct 27, 2026

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Genuine Parts

Warehouse Distribution Center Associate

Ontario, California, United States

NAPA Auto Parts is seeking a skilled and energetic Warehouse Associate to join our growing team of professionals. Our warehouse associates perform a variety of tasks including …

Added Nov 3, 2026

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Cencora

Warehouse Associate Nights

Mansfield, Massachusetts, United States

Part time

Pay posted by employer$37,752–$56,650

… area to keep pharmaceutical products and merchandise clean and help prevent work related injuries. Verify product received against receiving documents, notes and reports discrepancies and any obvious damages (dependent on …

Added Nov 10, 2026

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KLA

HQ Product Installation Upgrade Supervisor (Rapid Division)

Milpitas, California, United States

Full time
Regular

Pay posted by employer$95,600–$162,500 per year

… service organization that consists of Service Sales and Marketing, Spares Supply Chain management, Field Operations, Engineering, Product Training, and Technical Support. The KLA Services organization partners with our …

Added Oct 15, 2026

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Global Partners

Food Service Associate

Danbury, CT - Alltown

Pay posted by employer$18.13–$21.34

A fresh foods clerk is responsible for the daily operations of the stores deli/foodservice, ensuring a high level of sanitation, store appearance and customer service …

Added Nov 3, 2026

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Global Partners

Food Service Associate

Danbury, CT - Global

Pay posted by employer$17.49–$20.70

A fresh foods clerk is responsible for the daily operations of the stores deli/foodservice, ensuring a high level of sanitation, store appearance and customer service …

Added Nov 3, 2026

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Pfizer

Associate - Quality Systems

Visakhapatnam, Andhra Pradesh, India

Full time
Regular

… help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving …

Added Oct 16, 2026

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Cencora

Warehouse Associate - Days

Des Moines, Washington, United States

Full time

Pay posted by employer$37,752–$56,650

Added Oct 27, 2026

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Unum Group

Sales Consultant Associate- Maryland

Columbia, Maryland, United States

Full time

… of our entire team. Help us help others, and join Team Unum today! General Summary: The Sales Consultant Associate is in active development to be a marketing and technical expert who represents Unum – educating and …

Added Nov 3, 2026

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Unum Group

Sales Consultant Associate- Phoenix

Phoenix, Arizona, United States

Full time

Added Nov 3, 2026

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Unum Group

Sales Consultant Associate- Dallas

Addison, Texas, United States

Full time

Added Nov 3, 2026

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Unum Group

Sales Consultant Associate- Chicago

Chicago, Illinois, United States

Full time

Added Nov 3, 2026

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Unum Group

Sales Consultant Associate- Atlanta

Atlanta, Georgia, United States

Full time

Added Nov 3, 2026

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Visa

Sr. Associate Counsel

Mumbai, Maharashtra, India

… strategic legal advice and counsel to VAS, VCA and South Asia business teams regarding deal structures, product initiatives, commercial arrangements and regulatory matters. Serve as a trusted partner to business …

Added Oct 27, 2026

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Amgen

Study Delivery Sr Associate

India - Hyderabad

Full time
Regular

Job Description: Study Delivery Associate Role Name: Study Delivery Sr Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and …

Added Oct 15, 2026

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Apollo Global Management

Investment Reference Data Associate

El Segundo, California, United States

Full time
Regular

… & Experience Required Undergraduate degree with 3–6+ years of relevant experience in investment operations, security master, reference data, or asset servicing. Experience setting up and maintaining fixed income, …

Added Oct 27, 2026

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Campbell's

Part Time Sales Associate

USA - MI - Birch Run

Part time
Regular

… Build the Business Develop a strong working knowledge of store products and product-handling procedures. Use suggestive selling with customers, including offering the Behind-the-Counter …

Added Oct 28, 2026

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Amgen

Specialist Manufacturing New Product Introduction (NPI):Downstream Readiness

Holly Springs, North Carolina, United States

Full time
Regular

… in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies …

Added Oct 15, 2026

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Merck (MSD)

Associate Director , Data Stewardship

Hyderabad, Telangana, India

R419321 Associate. Director , Data Stewardship The Opportunity: Join a global biopharma company with a 130-year legacy and …

Added Oct 16, 2026

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Pfizer

Senior Clinical Research Associate

Taipei, Taiwan, Taiwan

Full time
Regular

The Senior Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials …

Added Oct 16, 2026

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Pfizer

Senior Clinical Research Associate

Taipei, Taiwan, Taiwan

Full time
Regular

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QUALIFICATIONS · employer excerpt

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience

1 more in the full description below.

About this opportunity

Original employer description

JOB SUMMARY

The Senior Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards.

The Senior Clinical Research Associate role is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders.

The Senior Clinical Research Associate is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner, and other members of the study team, as required, in activities associated with the set-up, running and close out of sites in a clinical trial.

JOB RESPONSIBILITIES

Responsible for investigator site management and monitoring for assigned sites:

Clinical Trial Monitoring:

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and Pfizer standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site initiation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meetings when required (virtual or F2F).
Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the Study Monitoring Plan, SOPs and commensurate with emerging issues and technologies.
Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics
Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues
Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines
Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities.
Support database release as needed
May undertake the responsibilities of an unblinded monitor where required

Clinical/Scientific and Site Monitoring Risk:

Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team
Interact with investigator site heath care professionals in a manner which enhances Pfizer’s credibility, scientific leadership and in order to facilitate Pfizer’s clinical development goals
Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators
Drive Quality Event remediation, when applicable
Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development andchecks, when applicable.

Other:

Mentor/train Clinical Research Associates as assigned
Serve as an SME for CRA-related processes
Participate in regional or local working groups/process improvement initiatives
Perform activities under guidance of a Site Care Partner prior to site activation e.g. feasibility and site selection, PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation
Conduct co-monitoring activities as requested

QUALIFICATIONS

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in both English and Mandarin.

PHYSICAL/MENTAL REQUIREMENTS

Advanced knowledge of clinical research and development processes and ability to gain command of process details

Demonstrated knowledge of global and local regulatory requirements
Advanced understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Advanced knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Proven ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required

ORGANIZATIONAL RELATIONSHIPS

Partners with Site Care Partner and Country SOM
Reports to Director of Clinical Site Operations, or Director of Site Management and Monitoring, or Site Care Partner III in some countries
When required Partners with other Study Team members e.g. Clinician, Recruitment Specialist, Clinical Data Scientist
Act as a mentor for Clinical Research Associates
Partner with other functional lines if engaged in a workstream/ LDT/ SME role

Work Location Assignment: Remote - Field Based

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

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Medical

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Full time
Medical
Regular

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