Job Description

Job Overview

We are seeking a highly skilled Project Manager II with a strong background in Biometric deliverables, including Data Management, Biostatistics, and Statistical Programming, specifically within the Life Sciences or CRO sector. This role offers an exciting opportunity to manage projects of moderate complexity while working collaboratively with cross-functional teams to ensure exceptional service delivery.

Key Responsibilities

  • Oversee the complete project management lifecycle, ensuring adherence to budget and schedule while achieving financial and operational KPIs.
  • Develop and manage project budgets, ensuring that financial targets are met and invoices are processed promptly.
  • Lead timeline development and scope management in accordance with established project management practices, regularly monitoring project progress and adjusting plans as necessary.
  • Identify, assess, and mitigate project risks and issues, collaborating with teams to devise effective solutions for seamless project execution.
  • Cultivate strong client relationships to enhance satisfaction, aiming for at least a 10% annual growth in revenue for assigned accounts.
  • Engage in activities such as RFIs, RFPs, and bid defenses, facilitating internal meetings and ensuring all objectives are accomplished.
  • Utilize advanced project management software and Excel tools for tracking project advancements, managing resources, and generating reports.
  • Maintain compliance with industry standards and regulations including ICH, 21 CFR Part 11, and ISO 9001:2000.

Required Skills

  • Proficiency in MS Office (Word, Outlook, PowerPoint) and advanced Excel capabilities.
  • In-depth understanding of clinical trial processes and the overall drug development lifecycle.
  • Excellent verbal and written communication skills, enabling effective collaboration with diverse teams and clients.
  • Strong organizational abilities with the capacity to juggle multiple tasks and deadlines efficiently.
  • Familiarity with project management software and regulatory knowledge of ISO 9001, ISO 27001, 21 CFR Part 11, FDA, and GCP regulations.

Qualifications

  • A bachelor’s degree is mandatory, or an equivalent combination of relevant experience.
  • Minimum of five years of experience in project coordination or management in a related field.
  • Familiarity with CROs and clinical trial terminology is advantageous.

Career Growth Opportunities

This position offers significant prospects for professional development within the project management domain, allowing you to refine your skills in overseeing complex projects while contributing to the organization’s ongoing success.

Company Culture And Values

We pride ourselves on a collaborative and supportive work environment that encourages proactive problem-solving and high-quality service delivery. Our team members are integral to project success, and we value strong relationships with our clients and internal teams.

Employment Type: Full-Time