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

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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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Cardinal Health

Warehouse Associate II (Mornings)

Memphis, Tennessee, United States

Cardinal Health - Warehouse Associate II Shift- Monday-Friday 5:00AM-1:30PM (or until task complete) Anticipated hourly range: $19.10 per hour - …

Added Oct 27, 2026

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Cardinal Health

Warehouse Associate II - Inventory

Memphis, Tennessee, United States

Cardinal Health - Warehouse Associate II Shift- Monday-Friday 4:00AM-12:30PM (or until task complete) Anticipated hourly range: $19.10 per hour - …

Added Oct 27, 2026

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Amgen

Senior Associate Quality Assurance

Thousand Oaks, California, United States

Full time
Regular

… part of the Amgen team. Join us and transform the lives of patients while transforming your career. Senior Associate Quality Assurance What you will do Let’s do this! Let’s change the world! The Sr. Associate Quality …

Added Oct 15, 2026

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BlackRock

Associate, Application Engineer

Bengaluru, Karnataka, India

Full time
Regular

… scalable platforms that distribute data to clients, integrate with strategic data platforms, and enable new product capabilities. Working closely with engineers, product managers, and data owners, you will contribute to the …

Added Oct 27, 2026

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Becton Dickinson

Associate Territory Manager - Boston

Boston, Massachusetts, United States

Field
Full time
Regular

Pay posted by employer$66,700–$106,700 USD

The Associate Territory Manager (ATM) is primarily responsible for providing field level support to physicians and other …

Added Oct 27, 2026

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Pfizer

Associate Manager - Microbiology

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 meets the highest standards of safety and efficacy. What You Will Achieve In this role, you …

Added Oct 16, 2026

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Cardinal Health

Warehouse Associate (2nd Shift)

OH-Columbus-Consumer Hub Logistics Center

The Warehouse Associate assists on Inbound or Outbound activities as requested by the Warehouse Supervisor meeting quality, safety, …

Added Oct 27, 2026

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S&P Global

Application Associate, SNL Feeds

Islamabad, Islamabad, Pakistan

Full time

Grade Level (for internal use): 07 Help shape the data product that powers the world's largest financial institutions. As an Application Associate, you'll sit at the …

Added Oct 27, 2026

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Target

Seasonal Full Time Hourly Warehouse Operations Openings (T3865)

3501 S Pulaski Rd, Chicago,IL 60623-4926

Pay posted by employer$22.75–$26.00 per hour

Current shift openings at this location:

Seasonal Warehouse Associate
Monday, Tuesday, Wednesday, Thursday 8:00AM-6:00PM
Wednesday, Thursday, Friday, Saturday …

Added Oct 19, 2026

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Target

Full Time Hourly Warehouse Operations Openings Only (T0587)

12735 E L Ave, Galesburg,MI 49053-9586

Pay posted by employer$20.70–$22.80 per hour

Current shift openings at this location:

Warehouse Associate
Tuesday, Wednesday, Thursday, Friday 6:00AM-4:00PM
Tuesday, Wednesday, Thursday, Friday …

Added Oct 16, 2026

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Target

Full Time Hourly Warehouse Operations Seasonal Openings (T0558)

875 Beta Dr SW, Albany,OR 97321-3714

Pay posted by employer$22.25–$24.75 per hour

of Warehouse Worker or Warehouse Associate based on your responses to the questionnaire and assessment you’ll complete during the application process. …

Added Oct 16, 2026

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Ingram Micro Holding

Sr Principal, Product Manager - Unified Support & AI Experience

Irvine, California, United States

… into a modern, AI-enabled global platform experience. We are looking for a visionary Senior Principal Product Manager to lead product strategy and roadmap execution for our Unified Support and AI Experience ecosystem. …

Added Nov 3, 2026

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Merck (MSD)

Associate Director, Vaccine Manufacturing

USA - Kansas - De Soto

Pay posted by employer$129,000–$203,100

Associate Director, Vaccine Manufacturing Join Us in Shaping the Future of Animal Health Our company is investing …

Added Oct 16, 2026

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Merck (MSD)

Associate Director, CMC

Beijing, Beijing, China +1 location

… and the lifecycle management. Technical Regulatory Support: Partner with regulatory colleagues on product specifications, quality control testing, and inspection-related matters; provide technical input and …

Added Oct 16, 2026

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Boeing

Associate Structural Design Engineer

USA - North Charleston, SC

In person

Pay posted by employer$85,000–$115,000

… system and component designs, using 3-D Computer Aided Design tools and/or other design methods, to provide product definition to other engineering groups, production operations, suppliers and external customers throughout …

Added Oct 12, 2026

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Becton Dickinson

Associate Territory Manager - Dallas

Dallas, Texas, United States

Field
Full time
Regular

The Associate Territory Manager (ATM) provides field-level support to customers and potential new customers in the …

Added Oct 27, 2026

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Capital One Financial

Sr Manager, Product Management - HR Products & Data

McLean, Virginia, United States +2 locations

Sr Manager, Product Management - HR Products & Data Product Management at Capital One is a booming, vibrant craft that requires …

Added Oct 30, 2026

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Capital One Financial

Senior Manager, Product Management - Machine Learning and AI

McLean, Virginia, United States +2 locations

Senior Manager, Product Management - Machine Learning and AI Senior Manager, Product Management (PXDP55) Product Management at …

Added Oct 27, 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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Keywords also found in description

Full time
Medical
Regular

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.