Project Manager II (CRO or Life Sciences) - Remote

ZipRecruiter; Canton (OH); Remote; USD 75,000 - 95,000; Full time

Job summary

A leading clinical research organization in Canton, Ohio is seeking a Project Manager to oversee project budgets and timelines while ensuring regulatory compliance. The ideal candidate has over 5 years of experience in project management within the clinical trials sector and a strong understanding of scientific principles. This full-time role offers an opportunity to enhance customer satisfaction and drive account growth.

Qualifications

• Minimum 5 years of project coordination or management experience.
• Strong knowledge of scientific principles.
• Experience with clinical trials and pharmaceutical development.

Responsibilities

• Develop budgets for moderate complexity projects.
• Independently develops project timelines.
• Handles daily project activities including risk management.

Skills

Project Management

Data Management

Biostatistics

Statistical Programming

Problem-Solving

Communication

Education

Bachelor’s Degree or relevant experience

Tools

MS Office

Excel (Hlookup, Vlookup, Pivot Tables)

Job description

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 science and regulatory expertise to help our clients develop and market life-changing therapies globally.

We value talented staff, continuous training, enthusiasm, collaboration, and teamwork, believing that diversity makes us stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

This position requires experience in Project Management, specifically supporting Biometric deliverables (Data Management, Biostatistics, Statistical Programming).

Responsibilities:

1. Develops budgets for moderate complexity projects, understanding various cost models.
2. Ensures financial KPIs are met, invoices on time, and updates revenue projections; manages project scope via established PM methodology and change management processes.
3. Independently develops project timelines of moderate complexity.
4. Uses MSP to understand task constraints, conveys critical milestones, and develops strategies to meet timelines.
5. Handles daily project activities including risk management, issue escalation, and resolution, collaborating with functional management.
6. Uses intermediate Excel skills (Hlookup, Vlookup, Pivot Tables, etc.).
7. Enhances customer satisfaction, develops account growth plans aiming for at least 10% annual revenue growth, and manages at least one key account.
8. Participates in or leads RFIs/RFPs, capabilities meetings (at least twice annually), and bid defenses (at least once annually).
9. Proficient in Word, Outlook, PowerPoint, and meeting facilitation.
10. Understands regulatory requirements: ICH, 21 CFR Part 11, ISO 9001:2000.

Qualifications:

1. Bachelor’s Degree or relevant experience.
2. At least 5 years of project coordination or management experience.
3. Strong knowledge of scientific principles.
4. Proficiency with MS Office.
5. Experience with clinical trials and pharmaceutical development.
6. Good communication, problem-solving, and organizational skills.
7. Familiarity with ISO 9001, ISO 27001, 21 CFR Part 11, FDA, and GCP standards.
8. Basic understanding of CROs, clinical data, and drug development processes.

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