Thermo Fisher Scientific

Thermo Fisher Scientific

Posted via Workday

Associate Project Manager - Labs

Apply by Oct 5, 2026

Posted Sep 29, 2026

Role at a glance

Job function
Product, Strategy & Operations Program & Project Management
Salary
Not Disclosed
Location
Remote - Virginia, United States
Work arrangement
Remote
Employment
Full-time
Experience
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’) or equivalent...
Education
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Visa support
Must be legally authorized to work in the United States without sponsorship.

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Role Summary

AI-generated

The Associate Project Manager - Labs supports clinical trial shipment and sample resolution and database import quality processes. The role liaises with operational departments, affiliates, and sponsors in support of identified protocols and study programs.

What You'll Do

  • Investigate clinical trial shipments and samples that cannot be clearly identified or routed upon receipt.
  • Review shipment documentation, manifests, and other relevant data to resolve shipment, manifest, and sample discrepancies.
  • Review database import requests for accuracy and consistency, and provide status information on pending and completed imports.
  • Implement quality control review procedures for data imports.
  • Participate in internal or self-audits of database content and support quality assurance and quality control procedures.
  • Perform corrective and preventative action activities and special projects to support quality assurance and quality event outcomes.

Generated from the employer's posting. Verify important details before applying.

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Qualifications

Requires a bachelor's degree or equivalent and relevant formal academic or vocational qualification, plus previous experience comparable to 0 to 2 years or an equivalent combination of education, training, and experience. Skills include organization and adaptability, project management, computer skills, general knowledge of clinical trial processes and programs, attention to detail, problem solving, written and verbal communication, resolving technical problems in a professional environment, applying procedural documents, and working well with others.

Required

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience comparable to 0 to 2 years or an equivalent combination of education, training, and experience
  • Organizational and project management skills; ability to adapt to changing priorities and manage multiple assignments with challenging...
  • Computer skills and general knowledge of clinical trial processes and programs
  • Attention to detail and problem-solving skills
  • Written and verbal communication skills
  • Experience identifying and resolving technical problems in a professional environment
  • Ability to attain, maintain, and apply working knowledge of applicable procedural documents

Original job description

Content provided by the employer

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

This is a fully remote role supporting our BioAnalytical Laboratory in Richmond, VA. We welcome applicants from all locations within the US.  

Must be legally authorized to work in the United States without sponsorship. 

Must be able to pass a comprehensive background check, which includes a drug screening. 


The working shift for this role is Monday - Friday from ~8AM-5PM.


Join Us as an Associate Project Manager - Labs – Make an Impact at the Forefront of Innovation

The Associate Project Manager - Labs liaises with PPD's operational departments, affiliates and sponsors. Supports the identification, evaluation, and resolution of shipments for identified protocols and/or study programs.

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

What You'll Do:
• Investigate clinical trial shipments and samples that cannot be clearly identified or routed upon receipt.
• Review available shipment documentation, manifests, and other relevant data to support resolution of shipment, manifest and sample discrepancies.

• Review requests for database imports for accuracy and consistency and provide accurate status information of all pending and completed database imports.
• Implement quality control review procedures to ensure accurate data imports.
• Participate in internal/self-audit of database content, supporting ongoing quality assurance and quality control procedures.
• Perform corrective and preventative action activities and special project activities, as required, to support ongoing quality assurance and quality event outcomes.

Education and Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’) or equivalent combination of education, training, & experience.

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities:
• Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
• Effective project management and organizational skills
• Good computer skills
• General knowledge of clinical trial processes and programs
• Strong attention to detail and problem solving skills
• Good written and verbal communication skills
• Demonstrated experience in identification and resolution of technical problems in a professional environment
• Ability to attain, maintain and apply a working knowledge of applicable procedural documents
• Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others

Working Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations, occasional domestic travel.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.

Why join us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

The salary range estimated for this position based in Virginia is $50,800.00–$67,700.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Thermo Fisher Scientific

About the company

Thermo Fisher Scientific

Large Enterprise

Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.