Vaga de Manager, COA Management, PCS
1 vaga: | Publicada em 17/05
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Role & Responsibilities
The IQVIA Patient Centered Solutions group has an opportunity for a Managerto join
the team to support COA Management 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 advanced analytics, technology solutions and
clinical research services to the life sciences industry. 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. Learn more at
https://jobs.iqvia.com