Job Details

Project Manager II (CRO or Life Sciences) - Remote

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About MMS
MMS is an innovative, data-focused CRO supporting the pharmaceutical, biotech, and medical device industries with a scientific approach to complex trial data and regulatory submissions. With a global presence across four continents, MMS maintains a 97% customer satisfaction rating.

Our mission is to deliver high-quality service and technology solutions rooted in strong science and decades of regulatory experience to help develop and market life-changing therapies worldwide.

MMS values talented staff, continuous training, enthusiasm, collaboration, and teamwork, recognizing that a diverse talent pool strengthens the company. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

This position requires expertise in supporting Biometric deliverables (Data management, Biostatistics, Statistical Programming services).

Responsibilities

• Develops budgets for moderate complexity projects, understanding various cost models.
• Ensures financial KPIs are met; invoices on time; updates revenue projections; controls project scope via PM methodology and change management processes.
• Creates moderate complexity project timelines independently.
• Uses MSP for advanced functions; understands task constraints; communicates critical milestones; develops strategies to meet timelines.
• Manages daily activities including risk identification, issue escalation, and resolution; collaborates with functional management.
• Proficient in Excel (Hlookup, Vlookup, Pivot Tables).
• Works to enhance customer satisfaction, develops account growth plans, and manages at least one key account aiming for 10% revenue growth annually.
• Participates in or leads RFIs/RFPs, capabilities meetings, and bid defenses.
• Proficient in Word, Outlook, PowerPoint; skilled in meeting facilitation.
• Understands ICH, 21CRF Part 11, ISO 9001:2000 requirements.

Minimum Requirements

• Bachelors Degree or relevant work experience.
• At least 5 years of project coordination or management experience.
• Scientific principles and concepts knowledge.
• Proficiency with MS Office.
• Experience with clinical trials/pharmaceutical development preferred.
• Good communication, problem-solving, and organizational skills.
• Familiarity with ISO 9001, ISO 27001, 21 CFR Part 11, FDA, GCP standards.
• Basic understanding of CROs, clinical data, and drug development process.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Project Management and IT
• Industry: Pharmaceutical Manufacturing

This job is active and accepting applications.