[Hiring] Project Manager II (Biometrics) @MMS

Role Description

We are looking for a full-time employee, remotely based within South Africa. This position requires proven Project Management experience in support of Biometric and Data deliverables (Data management, Biostatistics, Statistical Programming services).

• Understands various cost models and develops budgets for moderate complexity projects.
• Ensures financial KPIs are achieved on assigned projects; invoices on-time and ensures alignment with the contracted payment schedule; updates revenue projections on assigned projects.
• Controls project scope via defined PM methodology and processes for change management.
• Develops moderate complexity project timelines independently.
• Performs advanced functions in MSP. Understands task constraints and conveys critical path milestones to the functional lead. Develops/input into strategies to help achieve timeline expectations.
• Executes day-to-day activities during the course of a program/project including risk identification, issue escalation and resolution. Collaborates with functional line management to resolve any issues and trends.
• Intermediate excel skills (Hlookup, Vlookup, Pivot Table, etc.).
• Drives customer satisfaction and works to strengthen client relationships. Develops an account growth plan and consults with line manager to achieve a 10% revenue growth annually (minimum). Manages minimum one key account.
• Participates in or leads RFIs/RFPs in collaboration with proposals team. Participates in or leads capabilities meetings - at least 2 annually.
• Participates in or leads bid defenses - at least 1 annually.
• Proficient in Word, Outlook, PowerPoint.
• Proficient in meeting facilitation including scheduling, development of agendas and meeting minutes; works with project leads to ensure meeting objectives are met.
• Understands general requirements: ICH, 21CRF Part 11, and ISO 9001:2000.

Qualifications

• Bachelor’s Degree required, or relevant work experience.
• Minimum of 5 years’ experience in project coordination or project management 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 & clinical data/terminology, & the drug development process.

Requirements

• Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.