About MMS 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 MMS recognizes that a talented staff drives its business forward. The company focuses on identifying and attracting top talent and continuous training to strengthen core skills. Enthusiasm, collaboration, and teamwork are fostered, recognizing that a global and diverse talent pool makes the company stronger. Visit or follow MMS on LinkedIn for more information. We are looking for a full-time employee, remotely based within SA. Responsibilities Understand various cost models and develop budgets for moderate complexity projects. Ensure financial KPIs are achieved on assigned projects; invoice on time and align with contracted payment schedule; update revenue projections. Control project scope via defined PM methodology and change management processes. Develop moderate complexity project timelines independently. Perform advanced functions in MSP. Understand task constraints and convey critical path milestones to the functional lead. Develop input into strategies to help achieve timeline expectations. Execute day-to-day activities during the course of a program/project including risk identification, issue escalation and resolution. Collaborate with functional line management to resolve any issues and trends. Intermediate Excel skills (HLOOKUP, VLOOKUP, Pivot Table, etc.). Drive customer satisfaction and strengthen client relationships. Develop an account growth plan and consult with line manager to achieve at least 10% revenue growth annually. Manage at least one key account. Participate in or lead RFIs/RFPs in collaboration with proposals team. Participate in or lead capabilities meetings – at least 2 annually. Participate in or lead bid defenses – at least 1 annually. Proficiency in Word, Outlook, PowerPoint. Proficiency in meeting facilitation including scheduling, development of agendas, and minutes; work with project leads to ensure meeting objectives are met. Understand general requirements: ICH, 21 CFR Part 11, and ISO 9001:2000. Requirements Bachelor’s Degree required, or relevant work experience. Minimum of 2 years’ experience in project coordination or project management or similar field. Expert knowledge of scientific principles and concepts. Proficiency with MS Office applications. Hands‑on experience with clinical trial and pharmaceutical development preferred. Good communication skills and willingness to work with others to clearly understand needs and solve problems. #J-18808-Ljbffr