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. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO in Global Health & Pharma’s international awards programs for the last three consecutive years. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

Responsibilities: 

• Completes set-up of contracts within financial systems; creates projections versus actual spreadsheet for PM review; De-activate projects within ERP system and ensure all invoices have been generated; At close-out, perform financial reconciliation of invoicing versus actual contract per PM request.
• Performs basic functions within ERP system.
• Prepare, verify and carry out invoicing via electronic processing and reporting activities within specified deadlines for assigned portfolios; Close interaction with revenue team to ensure timely billing; Investigate and resolve customer financial queries; develop payment schedules from existing templates.
• Periodic reporting of project financial KPIs to Project Management and Finance Management, including investigation and root cause analysis; Assist in the implementation of financial reports that monitor MMS' financial health (i.e.. %BO, CPI, Financial by department or deliverable, etc.).
• Intermediate excel skills (Hlookup, Vlookup, Pivot Table, etc.).
• Proficient in Word, Outlook, PowerPoint.
• Understands general requirements.

Requirements:

• College graduate Business, Accounting, Finance discipline or related field, or related experience.
• Minimum of 5 years’ experience in a project billing role or similar field required.
• 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.         
• Excellent problem-solving skills.        
• Good organizational and communication skills.       
• Familiarity with current ISO 9001 and ISO 27001 standards preferred.        
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.           
• Basic understanding of CROs and scientific and clinical data/ terminology, and the drug development process.