OptymEdge - Manager, Ophthalmic Certification Project Management Group - Rockville, United States - Emmes

    Emmes
    Emmes Rockville, United States

    1 week ago

    Default job background
    Regular Full time
    Description

    Overview

    Manager, Ophthalmic Certification Project Management Group

    US Remote

    The Emmes Company, LLC ("Emmes") is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass.

    Our "Character Achieves Results" culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. We are a trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research.

    If you share our motivations and passion in research, come join us You will be joining a collaborative culture that empowers every Emmes employee — from entry level through top executive — to contribute to our clients' success by sharing ideas openly and honestly.

    Primary Purpose

    The Manager, Ophthalmic Certification Project Management Group (OCPMG) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical-sponsored clinical trials, as a matrix leader of a vendor project team. The Manager, OCPMG will be client-facing and serve as the internal lead of the project through the life cycle of the study, ensuring effective project delivery in agreement with contracted project timeline and budget. The Manager, OCPMG directs project delivery by driving team and financial efficiency, work product quality, and is responsible for client satisfaction through strong relationship management. The Manager, OCPMG works closely with the Ophthalmic Certification Project Management leadership to ensure compliance with operational tasks, Standard Operating Procedures (SOPs) and overall ophthalmic certification objectives.

    Responsibilities

  • Accountable for the training, performance management, and mentoring of assigned Project Managers
  • Provides ongoing coaching and feedback to Project Managers, including addressing
  • performance issues, conducting formal performance appraisals, and creating development plans. Escalates performance issues to Director, Ophthalmic Project Management

  • Coordinates Project Team Meetings, including the development of meeting agendas and minutes
  • Ensures training occurs and evaluates proficiency or additional training needs of Project Management (PM) staff
  • Tracks PM utilization with the goal to ensure at least 90% utilization of all staff
  • Motivates and develops the team
  • Develops and oversees recruitment and retention strategies for the Ophthalmic Certification Project Management Group
  • Serves as the primary point of contact for biopharma clients and demonstrates proficiency in knowledge and understanding of client needs
  • Ensures that deliverables for the assigned projects are completed according to the contract budget, schedule, and quality standards. Projects will be effectively managed in all areas of performance
  • Develops successful working relationships with clients, executive management, and project staff and collaborates to manage project issues, proactively identify and mitigate risks and drive milestone achievement
  • Tracks project deliverables against contract. Proactively prepares/presents study metrics to maintain transparency for internal/external stakeholders. Monitors trends and drives changes to the plan as needed; identifies risks to delivery and agrees to mitigation plans with the project team to be presented to the client
  • Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables
  • Identifies and manages changes to scope and requests for out-of-scope activities. Collaborates with Business Development, Contracts Department, and executive management to ensure timely execution of contract amendments/change orders. Prospectively manages client expectations
  • Supports development of Requests for Proposal (RFPs) for biopharma clients in collaboration with leaders and key subject matter experts (SMEs)
  • Models and propagates Emmes' commitment to a culture of quality in all aspects of our deliverables, utilizing a solution-based, science-driven, value-added approach in collaborating with clients
  • Supports internal stakeholders on departmental initiatives upon request
  • Contributes to the development and maintenance Ophthalmic Certification Project Management SOPs and processes in collaboration with department leads
  • Supports the identification and implementation of tools and process integrations that support the efficiency and productivity of the OCPMG. This may include but is not limited to collaboration with internal stakeholders and vendors to support global, OCPMG efficiency and standardization with the department
  • Performs other duties as assigned
  • Qualifications

  • Bachelor's degree preferred or equivalent experience will be considered
  • Minimum 6 years demonstrating related experience, with 3 years working in a pharmaceutical and/or Clinical Research Organization (CRO) setting
  • 2 years of related supervisory experience
  • Demonstrated experience with MS Office Suite, particularly MS Word
  • Time management and decision-making skills
  • Attention to detail and the ability to address several assignments simultaneously
  • Excellent oral and written communication skills
  • Some knowledge of clinical trials in ophthalmology preferred
  • Emmes requires all US based Clinical Research Associate new hires to be fully vaccinated before their first day of employment. All new hires may also be required to comply with other COVID-19 health and safety protocols, such as masking or testing. Emmes complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons.

    Why work at Emmes?

    At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

  • Unlimited Approved Leave
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment