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    Job · 16765601

    PrimeVigilance logo

    Project Manager ( Pharmacovigilance )

    PrimeVigilance · Noida · onsite · Posted 43d ago

    Not disclosedFresherfulltimeSourced fromFoundit

    About a minute. You'll make an account on the way through.

    About this role

    Company Description

    Safety science and technology move forward here. So will you.

    Prudentia, a PrimeVigilance company, is where safety science meets technology. We advise pharmaceutical companies on the processes and systems behind clinical and post-marketing safety, from selecting and implementing safety databases to managed services, data migration and turnkey tools that close the gaps in leading safety platforms.

    It is specialist, high-trust work, and it depends on people who love solving hard problems. We are a team of curious minds, problem-solvers and experts brought together by a shared commitment to patient safety and to doing meaningful work well. Our culture values kindness, flexibility, growth and belonging, and we back one another to keep learning.

    If you want a role with purpose, room to grow and the chance to make a real difference, we would love to hear from you.

    Job Description

    Bridges the gap between individual project delivery and overarching program strategy, managing clusters of

    related projects.

    Role And Responsibilities

    • Coordinate PMO activities as directed
    • Manage project scope, schedule, and costs
    • Maintain good client relations
    • Oversee task delivery and interim milestones.
    • Ensure assigned project tasks are delivered within budget and on time
    • Act as a secondary point of contact for clients.
    • Track risks/issues to closure
    • Status reporting to customer
    • Manage changes to project scope
    • Perform advanced financial analysis
    • Oversee Quality Management System activities for the client.
    • Coordinate inter-project dependencies
    • Consolidate reporting across multiple project streams
    • Manage project escalations.

    Additional Responsibilities

    • Support Program Managers in strategic planning
    • Contribute to client governance meetings.
    • Practice Development (PD)
    • Leads development of internal process docs (eg SOPs) and training materials
    • Leads development of articles, brochures, whitepapers, POVs
    • Identifies required PD activities
    • Estimates budget for PD activities
    • Additional Service offerings (SO)
    • Well versed in 2+ SOs
    • Leads small project or work stream
    • Recruiting
    • Identifies candidates from personal networks
    • Assists with recruiting blitz as directed
    • Conducts technical interviews
    • Conduct culture / fit interview
    • Author job description as directed
    • Sales
    • Represents company at bid defense
    • Authors components of proposal
    • Participates at conferences
    • Identify new opportunities with existing clients
    • Leads demos
    • Admin
    • Completes all admin tasks (e.g. time reporting, training records) timely with high quality
    • Conduct appraisals for team members
    • Review team T&E

    Qualifications

    Education

    Bachelor's degree in pharmaceutical sciences, healthcare management, information technology, or a related field; PMP Certification preferred

    Experience

    • Ability to lead and motivate teams
    • Able to provide training to new hires and colleagues with good mentoring and coaching skills
    • Advanced resource allocation skills
    • Proactive approach to work with high level of commitment
    • Able to work well in a team environment
    • Good attention to detail, time management and organisational skills
    • Good communication and interpersonal skills
    • Structured and methodical approach to work with good analytical and problem-solving skills
    • High level of quality consciousness
    • Able to take ownership of assigned processes
    • Ability to work under pressure
    • Able to work independently with minimum supervision
    • Ability to evaluate data and draw conclusions independently
    • Able to design innovative solutions
    • Good note-taking ability
    • Able to generate enthusiasm and drive for commitment to excellence
    • Strong presentation skills and ability to deliver informative, well-organised presentations to team and management
    • Confident decision maker
    • Advanced conflict resolution skills
    • Strategic thinking
    • Cross-functional collaboration

    Additional Information

    When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

    We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.

    • Quality: we hold ourselves to the standard patients deserve.
    • Integrity and trust: we do the right thing, especially when it is hard.
    • Drive and passion: we care about the outcome, because someone is waiting on it.
    • Agility and responsiveness: we move quickly, because patients cannot wait.
    • Belonging: everyone is welcome, and every voice counts.
    • Collaborative partnerships: we go further by going together.

    We look forward to welcoming your application.

    Sourced from foundit

    Skills

    RecruitingQuality Management SystemCross-Functional CollaborationClient Relationspresentation skillsStatus ReportingConflict ResolutionResource Allocationfinancial analysis

    About PrimeVigilance

    PrimeVigilance logo

    PrimeVigilance

    501-1000

    employees

    2008

    18 years old

    Guildford

    United Kingdom

    ₹9.7L PA avg

    Avg at PrimeVigilance

    About

    PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.
    From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.
    • 900+ highly qualified professionals
    • Global leader in QPPV services
    • 24/7 multilingual call center
    • Choice of leading drug safety databases
    • Robotic Process Automation (RPA) expertise
    • Access to regulatory experts and key opinion leaders

    GLOBAL LIFE CYCLE MANAGEMENT SERVICES
    • PHARMACOVIGILANCE
    • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT
    • AUDIT & INSPECTION
    • QUALITY MANAGEMENT
    • REGULATORY SCIENCE

    Industries

    Health CareInformation TechnologyMedical

    Employee ratings

    9 reviews

    3.3/ 5

    Culture

    3.4

    Career growth

    2.9

    Work-life

    3.7

    Employees rate it well for

    Work-Life Balance35Work Satisfaction34

    Find them on

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