Senior Project Manager

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We have an incredible opportunity for a Project Manager to join our Real World Evidence/Late Phase team.

As a Project Manager within our Real World Evidence/Late Phase team, you will expect to add towards a culture of project group excellence with a focus on process improvement, adding value and exceeding client needs.

Location: Brazil, Mexico or Argentina (Remote)

Summary:

You will be the point of contact for designated projects, responsible to deliver successful client relationships, lead cross-functional teams, define project scope, build resource requirements, risk migration strategies, associate action plan and issue resolution.

Our projects range from phase II safety and efficacy trials to large scale outcomes mega-trials. You have the support of extraordinary, tenured and experienced leadership whose goal is to help you apply and expand your project management, drug development and therapeutic expertise.

​Highlights of Key Responsibilities:

• Planning and implementation of cross-functional project(s).

• Facilitate the definition of project scope, goals and deliverables

• Define project tasks and resource requirements.

• Develop full-scale cross-functional project plans.

• Assemble and coordinate project staff

• Plan and schedule project timelines

• Develop and Manage Risk Mitigation Strategies for projects

• Track project deliverables using appropriate tools

• Constantly monitor and report on progress of the project to all stakeholders

• Implement and manage project changes and interventions to achieve project outputs

• Project evaluations and assessment of results

• Manage project study budgets and invoicing procedures according to study contract

Requirements:

• At least 2 year PM experience within clinical research and study operations

• Bachelor’s Degree in science, business, medicine or equivalent degree

• Vaccines experience and/or COVID experience is a plus

• Project Management or equivalent (PMI certification) desirable

• Strength in communication, planning, decision-making, negotiation, conflict management and time management skills

Benefits of Working in ICON: