Job Description
This is a fantastic opportunity for an experienced Project Manager with a background in supporting Biometric deliverables (Data Management, Biostatistics, Statistical Programming) within the life sciences or CRO space. The ideal candidate will have a passion for managing projects with moderate complexity, collaborating with cross-functional teams, and ensuring high-quality service delivery.
You will oversee the end-to-end project management process, ensuring that projects stay on budget, on schedule, and meet the required financial and operational KPIs. This role is perfect for someone with advanced project management skills, strong attention to detail, and a proactive approach to problem-solving.
Key Responsibilities:
Project Financial Management: Develop and manage project budgets for moderate complexity projects. Ensure financial KPIs are met, invoices are submitted on time, and revenue projections are updated regularly.
Scope and Timeline Management: Lead the development of project timelines and ensure the scope is managed according to established project management methodologies. Track project progress and adjust timelines as necessary.
Risk and Issue Management: Proactively identify project risks and issues, escalate as needed, and collaborate with teams to resolve them. Provide guidance and solutions to ensure smooth project execution.
Customer Satisfaction: Foster strong relationships with clients to drive satisfaction. Work to achieve a minimum 10% revenue growth annually for assigned accounts and contribute to the growth of the client portfolio.
Collaboration: Participate in or lead requests for information (RFIs), proposals (RFPs), and bid defenses. Engage with internal teams to facilitate meetings, including setting agendas, taking minutes, and ensuring objectives are met.
Tools & Systems: Utilize advanced project management software (such as MSP) and Excel (Hlookup, Vlookup, Pivot Tables) to track project progress, manage resources, and create reporting tools.
Compliance and Best Practices: Maintain familiarity with industry standards such as ICH, 21 CFR Part 11, and ISO 9001:2000 to ensure all projects comply with regulatory requirements.
Qualifications:
Education: Bachelor's degree required, or equivalent relevant experience.
Experience: At least 5 years of experience in project coordination or project management in a related field.
Industry Knowledge: Strong understanding of scientific principles, clinical trial processes, and the drug development lifecycle. Familiarity with CROs and clinical/clinical trial terminology is a plus.
Technical Skills: Proficiency in MS Office (Word, Outlook, PowerPoint) and advanced Excel skills. Experience with clinical trial or pharmaceutical development preferred.
Communication & Problem-Solving: Excellent communication skills with the ability to work effectively with various teams and clients. Strong organizational skills and the ability to manage multiple tasks and deadlines simultaneously.
Regulatory Knowledge: Familiarity with ISO 9001, ISO 27001, 21 CFR Part 11, FDA, and GCP regulations.
Employment Type: Full-Time
Salary: $ 115,000.00 Per Year
Job Tags
Full time, Remote job,