MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Job Responsibilities:
- Interpret and assess requests for proposal (RFPs) or requests for information (RFIs) and build a response that addresses Sponsor requirements and provides a compelling message differentiating our offering.
- Coordinate with Business Development Leads and subject matter experts throughout the company to build an operational strategy to address the Sponsor’s needs.
- Coordinate with SMEs to provide responses to Sponsor-specific questions and concerns.
- Collect specifications and details from SMEs and build a budget that clearly outlines the appropriate deliverables, pricing, resourcing and timelines.
- Support the defense of proposals and pricing to Sponsors as well as to internal approvers.
- Continuously improve the process of developing proposals and budgets, incorporating technology where appropriate, to more efficiently provide deliverables, check for quality gaps, and effectively manage communication.
- Support the maintenance of internal proposal and response libraries.
- Advanced understanding of CROs and scientific & clinical data/terminology, & the drug development process.
- 3 to 6 years’ experience in the CRO industry in proposals, pricing, and/or other related roles.
- Bachelors’ Degree in Scientific Discipline, Finance, or equivalent experience. Advanced degree is preferred.
- Highly proficient with effectively organizing and maintaining records related to proposals and contracts using CRM, SharePoint (SPO). Highly compliant with Commercial Operations records retention processing including file naming convention, folder organization and status updates in CRM.
- Ability to map budgets into client grid and use client systems such as Ariba or Workday.
- Effectively sets and manages priorities to ensure efficient and timely outcomes to satisfy internal and external customers.
- Highly proficient managing lifecycle of assigned deliverables.
- Demonstrated expertise in reviewing, validating, and quality-controlling budgets prepared by others.
- Extensive experience in authoring and managing complex proposals.
- Highly proficient with MS Office Applications: Word, Excel, PowerPoint, Outlook, etc.
Skills Required
- Advanced understanding of contract research organizations, scientific and clinical data terminology, and the drug development process
- 3 to 6 years of experience in the CRO industry in proposals, pricing, or related roles
- Bachelor's degree in a scientific discipline, finance, or equivalent experience
- Experience organizing and maintaining proposal and contract records using CRM and SharePoint
- Compliance with Commercial Operations records retention processes, file naming conventions, folder organization, and CRM status updates
- Ability to map budgets into client grids and use client systems such as Ariba or Workday
- Ability to set and manage priorities to achieve timely outcomes
- Experience managing the lifecycle of assigned deliverables
- Expertise reviewing, validating, and quality-controlling budgets prepared by others
- Extensive experience authoring and managing complex proposals
- Advanced degree
- Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook
What We Do
MMS is an award-winning, global clinical research organization (CRO) that supports leading pharmaceutical and biotech companies as well as many smaller enterprises across our spectrum of services. Having completed more than 50 submissions for drug approval over the last 5 years, we remain a top choice for sponsors who are looking for innovation and demand high quality from their CRO partners. Senior leadership at MMS has more than two decades of hands-on drug development experience which helps support program-level strategy and execution of projects across multiple therapeutic areas. Continual staff training, innovative recruitment and motivating career opportunities help MMS retain the best talent and develop a strong, client-focused workforce across all global locations. Our mission is to deliver high-quality services, rooted in good science and decades of regulatory experience, that will assist our clients in developing and marketing life-changing therapies, thereby positively affecting patients' lives worldwide.







