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Home Flexible Job Board Manager, Global Proposals

$95,000–110,000/yr 9d ago

Manager, Global Proposals

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QPS, LLC

Newark, DE, US

Full-time Permanent Remote

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Summary

The Manager, Global Proposals will lead the development of competitive budgets and proposals for full-service clinical trials while coordinating with global cross-functional teams. They are responsible for managing the RFP process, ensuring pricing accuracy, and mentoring team members within the Global Proposal Office.

Job Description

QPS is a global contract research organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies throughout the drug development process. Our services span Bioanalysis, Drug Metabolism and Pharmacokinetics (DMPK), Toxicology, Translational Medicine, Early Phase Clinical, and Phase II–IV Clinical Research.

We are looking for a US-based experienced clinical proposal and contract professional to join our Global Proposal Office. This is a hands-on role for someone who enjoys developing proposals, budgets and contracts for USA, Europe and Asia while also working with colleagues based in USA, Europe and Taiwan. 

The Job

As Manager, Global Proposals, you will support the development of budgets and proposals for full-service clinical trials, with a primary focus on patient studies. You will have experience in developing/reviewing contracts for USA, Europe and Asia. You will work closely with Business Development, Clinical Operations, Finance, Contracts, and other subject matter experts to develop competitive, accurate proposals that reflect study requirements and operational assumptions.

You will also work within a team of where you work independently to complete and prioritize your proposal work, monitoring timelines, and supporting other members as a back-up of the Global Proposal Office. This role is a good fit for someone who wants to be hands-on, while working with Business Development and internal SMEs to create and finalize proposals and budgets in a client-ready format.

Key responsibilities include:

  • Develop and review budgets and proposals for full-service, multi-site clinical trials.
  • Coordinate proposal timelines, assignments, priorities, emails responses, client clarifications and your workload in order to deliver according to client timelines.
  • Lead selected complex or high-priority proposals from RFP through final submission.
  • Review proposals and budgets for accuracy, consistency, competitiveness, and alignment with protocol and operational assumptions.
  • Work closely with Business Development on RFP intake, bid strategy, pricing, and risk considerations.
  • Partner with Clinical Operations, Finance, Contracts, and subject matter experts to confirm scope, assumptions, timelines, and costs.
  • Support and mentor team members and serve as a resource for questions or more complex assignments.
  • Use advanced Excel skills for pricing, budget development, margin analysis, and scenario planning.
  • Maintain accurate proposal and opportunity information in Salesforce and related systems.
  • Help identify opportunities to improve proposal processes, tools, consistency, and efficiency.
  • Support a smooth handoff of awarded studies to operational teams.

Work Location

  • This job will be home-office based (see Telecommuting Policy for full details)

What We’re Looking For

  • Strong experience developing budgets and proposals for clinical trials in patient studies from a CRO.
  • Experience with full-service, multi-site patient studies, CRO contracting across USA, Europe and Asia.
  • Experience in clinical trials understanding how full-service proposals and budgets are created, and the background for how a clinical trials are performed.
  • Demonstrated ability to manage multiple proposals, competing deadlines, and changing priorities.
  • Strong understanding of clinical trial operations and the factors that drive study scope, timelines, and cost.
  • Strong Excel skills, including experience with complex budgets, pricing models, or financial analysis.
  • Clear communication skills and the ability to work effectively with global, cross-functional teams.
  • Strong attention to detail with a practical, solutions-focused approach to proposal development.
  • Ability to work independently and adjust working hours when needed to support global teams, client deadlines, and periods of high proposal volume.
  • Bachelor’s degree in Life Sciences, Business, Finance, or a related field, or equivalent relevant experience.
  • Approximately 5+ years in CRO budgets, proposals and contracting in a Full Service CRO that includes Project Management, CRAs, Medical Writing, Medical Monitoring, Safety/PV, Data Management, Biostatistics, and PK.
  • Salesforce or similar CRM experience is preferred.

A few important details

  • Because this role supports a global team, candidates located in the Eastern U.S. time zones are preferred.
  • We are not accepting agency submissions for this position at this time. 
  • This position is not eligible for employer-sponsored visa support; candidates must be authorized to work in the U.S. without current or future employer-sponsored visa support.

Why QPS?

At QPS, you will join a collaborative global team supporting a wide range of clinical research programs. You will have the opportunity to work on complex studies, contribute to how our Global Proposal Office operates, and take on meaningful team leadership responsibilities while remaining closely involved in the work itself.

QPS offers a competitive salary and benefits package, remote work, and the opportunity to work with colleagues across our global organization.

If you have strong clinical proposals experience and enjoy balancing hands-on work with team coordination and leadership, we would like to hear from you.

Equal Opportunity Employer

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

#LI-DNI

About the company

QPS, LLC

QPS is a GLP/GCP-compliant contract research organization (CRO) delivering the highest grade of discovery, preclinical, and clinical drug development services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction and turnkey laboratories and facilities. We are passionate about our work, creating value for patients and customers while generating opportunities for employees to thrive.

Since 1995, it has rapidly expanded from a tiny bioanalysis shop to a full-service CRO with 1100+ employees in the US, Europe, India and Asia. Today, it offers expanded pharmaceutical contract R&D services with special expertise in Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, and Clinical Development.

Through continual enhancements in capacities and resources, QPS stands tall in its commitment to deliver superior quality, skilled performance and trusted service to its valued customers.

Founded

1995

Company size

1,001-5,000 employees

Industry

Pharmaceutical Manufacturing

Org type

Privately Held

Headquarters

Newark, DE

Apply Now

About the company

QPS, LLC

QPS is a GLP/GCP-compliant contract research organization (CRO) delivering the highest grade of discovery, preclinical, and clinical drug development services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction and turnkey laboratories and facilities. We are passionate about our work, creating value for patients and customers while generating opportunities for employees to thrive.

Since 1995, it has rapidly expanded from a tiny bioanalysis shop to a full-service CRO with 1100+ employees in the US, Europe, India and Asia. Today, it offers expanded pharmaceutical contract R&D services with special expertise in Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, and Clinical Development.

Through continual enhancements in capacities and resources, QPS stands tall in its commitment to deliver superior quality, skilled performance and trusted service to its valued customers.

Founded

1995

Company size

1,001-5,000 employees

Industry

Pharmaceutical Manufacturing

Org type

Privately Held

Headquarters

Newark, DE

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