Associate Clinical Project Manager, Real World Evidence
Dubai, AE
منذ 1 ساعة
source : DirectEmployers Association

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers and patients.

Our approach is unique in the industry and is defining the way companies can develop and apply real-world evidence to provide deeper insight about market dynamics, therapy area changes, outcomes research and other scientific insights.

We are collaborative, intellectually curious, entrepreneurial and constantly looking for opportunities to harness the value of real-world evidence in a constantly evolving industry.

RWE Project Management is at the cornerstone of our study delivery and responsible for ensuring high-quality delivery to help our customers generate critical evidence.

RWE Project Management is creating and delivering the next generation of late phase studies, emphasizing creative problem solving and looking for individuals interested in changing the way research is conducted.

Job OverviewAssociate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster.

The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.

Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.

The Associate Project Lead support the efforts of CPM to drive operational excellence and strategic leadership with our customers.

Associate Project Leads may run their own studies, as part of their development.Essential Functions

  • Provide input in to the development of integrated study management plans with the core project team and / or sub-team.
  • Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
  • Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
  • Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
  • Monitor progress against contract and prepare / present project and / or sub-team information proactively to internal stakeholders.
  • Support the project leader to prepare / present project and / or sub-team information proactively to external stakeholders.

  • Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
  • Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning / implementing appropriate corrective and preventative action plans.
  • May serve as primary (for small projects) or back-up project contact with customer.
  • Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
  • Support the project leader in ensuring the financial success of the project.
  • Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
  • Identify changes in scope and partner with project leader to manage change control process as necessary.
  • Identify lessons learned and implement best practices.
  • May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirementsQualifications
  • Associate's Degree In life sciences or related field required Req Or
  • Bachelor's Degree In life sciences or related field required Req
  • 2 years clinical research experience.
  • Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.;
  • Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements , regulations and guidelines, towards clinical trial conduct.
  • Broad protocol knowledge, therapeutic knowledge desired.;
  • Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
  • Problem solving - Strong problem solving skills.
  • Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
  • Prioritisation - Ability to handle conflicting priorities.
  • Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
  • IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
  • Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Strong customer service skills.

  • Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
  • Finances - Good understanding of project financials.
  • IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
  • At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.

    The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.

    Learn more at IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward.

    Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

    To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health.

    Thank you for your interest in growing your career with us.EEO Minorities / Females / Protected Veterans / Disabled

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