Project Manager: Clinical Research, PCS

IQVIA

Cataluña

On-site

EUR 70,000 - 110,000

Full time

6 days ago
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Job summary

IQVIA is seeking a Manager to join the Patient Centered Solutions group to support licensing and electronic implementation of COAs for clinical trials. You will lead COA licensing operations, coordinate with vendors and internal teams, and monitor performance including revenue tracking.

The role requires a life sciences degree, 4+ years in clinical research or vendor management, and 2+ years in a project management or client-facing role, with strong English communication.

Qualifications

  • Bachelor's degree or equivalent in life sciences or related disciplines.
  • 4+ years in clinical research, medical affairs, vendor management, or similar.
  • 2+ years in a Project Management, Consulting, or client-facing role.
  • Solid understanding of the pharmaceutical industry and drug development.
  • Fluency in English (spoken and written).
  • Strong communication, presentation and interpersonal skills.
  • Excellent planning and time management.

Responsibilities

  • Oversee and manage the operational aspects of COA licensing activities from study initiation through closeout; partner with study PMs and set up vendors.
  • Create, track and report COA licensing project support timelines.
  • Provide financial reporting on COA licensing projects including tracking deliverables and invoicing.
  • Monitor, manage, and communicate COA licensing activities to cross-functional project teams.
  • Coordinate with project resources inside and outside the organization.
  • Negotiate COA licensing costs and contracts.
  • Develop and maintain internal databases of COA licensing requests and project plans.
  • Participate in proposal development and sales/presentation for COA licensing.
  • Meet with team members regularly to ensure milestones are met.
  • Ensure work aligns with standard processes and meets timeline metrics.

Skills

Project management
Vendor management
Client communication
Time management
Problem solving
Interpersonal skills
English fluency

Education

Bachelor's degree in life sciences

Tools

MS Office

Job description

Role & Responsibilities

The IQVIA Patient Centered Solutions group has an opportunity for a Manager to join the team to support Licensing & Distribution activities. In this role you will be responsible for managing the licensing and electronic implementation processes of Clinical Outcome Assessments (COAs) to be used in Clinical Trials, serving as primary contact with external vendors and internal departments. Also accountable for tracking the performance of assigned COAs businesses, including sales/revenue and staff allocation.

Specifically, your role will include:

  • Oversight and management of the operational aspects of COA licensing activities and programs from study initiation through to closeout including partnering with study project managers, setting up of vendors within IQVIA systems, facilitating legal reviews/approvals, and ultimately ensuring quality deliverables are on time and within budget.
  • Creating, tracking and reporting on COA licensing project support timelines.
  • Financial reporting on the COA licensing projects including tracking deliverables and invoicing.
  • Monitoring, managing, and communicating expectations and activities related to COA licensing to cross-functional project teams.
  • Coordinating with other project resources within and outside the organization.
  • Negotiating COA licensing costs and contracts.
  • Developing and maintaining internal databases of COA licensing requests and project plans.
  • Participating in proposal development and sales/proposal presentations for COA licensing.
  • Meet with team members on a regular basis regarding project tasks to ensure project milestones are met.
  • Ensure that work is conducted in compliance with standard processes, policies and procedures and meets project timeline metrics.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Bachelor's degree or equivalent in life sciences, other sciences, or related disciplines.
  • 4+ years’ work experience in clinical research, medical affairs, vendor management, or other related scientific roles.
  • 2+ years’ work experience in a Project Management, Consulting, or other similar client facing role.
  • Solid understanding of the pharmaceutical industry and drug development process.
  • Fluency in English (spoken and written).
  • Excellent communication, presentation and interpersonal skills including the ability to communicate effectively with both technical and non-technical audiences.
  • Results and detail-oriented approach to work delivery and output and excellent problem-solving skills.
  • Excellent planning, time management and prioritization skills.
  • Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
  • Ability to think and develop initiatives independently in alignment with the expectations of usual Project Management approaches.
  • Sound judgement and ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Strong software and computer skills, including MS Office applications.
  • Familiarity with IQVIA business units / functions and ability to navigate the organization effectively is a plus

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

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