MMS
Overview
Project Manager II (CRO or Life Sciences) - Remote
– position with MMS, a data-focused CRO supporting the pharmaceutical, biotech, and medical device industries. This role requires proven project management experience in supporting marketing applications and in the development and management of Risk Evaluation and Mitigation Strategies (REMS) programs. Our mission is to deliver high-quality service and technology solutions rooted in science and regulatory experience to help clients develop and market life-changing therapies. MMS values enthusiasm, collaboration, and teamwork in a global, diverse environment. Responsibilities
Understands various cost models and develops budgets for moderate complexity projects. Ensures financial KPIs are achieved on assigned projects; invoices on-time and aligns 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 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 issues and trends. Intermediate Excel skills (Hlookup, Vlookup, Pivot Table, etc.). Drives customer satisfaction and strengthens client relationships. Develops an account growth plan and, with the line manager, aims for a minimum 10% revenue growth annually. Manages at least one key account. Participates in or leads RFIs/RFPs in collaboration with the 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, developing agendas and meeting minutes; coordinates with project leads to ensure meeting objectives are met. Understands general requirements: ICH, 21 CFR 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. 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, and the drug development process. Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Project Management and Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at MMS. Get notified about new Project Manager jobs in Canton, MI.
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Project Manager II (CRO or Life Sciences) - Remote
– position with MMS, a data-focused CRO supporting the pharmaceutical, biotech, and medical device industries. This role requires proven project management experience in supporting marketing applications and in the development and management of Risk Evaluation and Mitigation Strategies (REMS) programs. Our mission is to deliver high-quality service and technology solutions rooted in science and regulatory experience to help clients develop and market life-changing therapies. MMS values enthusiasm, collaboration, and teamwork in a global, diverse environment. Responsibilities
Understands various cost models and develops budgets for moderate complexity projects. Ensures financial KPIs are achieved on assigned projects; invoices on-time and aligns 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 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 issues and trends. Intermediate Excel skills (Hlookup, Vlookup, Pivot Table, etc.). Drives customer satisfaction and strengthens client relationships. Develops an account growth plan and, with the line manager, aims for a minimum 10% revenue growth annually. Manages at least one key account. Participates in or leads RFIs/RFPs in collaboration with the 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, developing agendas and meeting minutes; coordinates with project leads to ensure meeting objectives are met. Understands general requirements: ICH, 21 CFR 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. 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, and the drug development process. Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Project Management and Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at MMS. Get notified about new Project Manager jobs in Canton, MI.
#J-18808-Ljbffr