Associate Project Manager

Pharmaceutical Research Associates, Inc; Brasil; Presencial; USD 30.000 - 70.000; Tempo integral

Resumo da oferta

Join a forward-thinking company as an Associate Project Manager, where you will be instrumental in coordinating clinical trials and advancing innovative treatments. This role offers the opportunity to work collaboratively with cross-functional teams, ensuring project milestones are met while developing essential study documents. You will leverage your project management expertise to enhance planning efficiency and data quality, all within a supportive and inclusive environment. With a focus on well-being and work-life balance, this organization is committed to nurturing talent and fostering a diverse culture that rewards high performance. If you are passionate about making a difference in healthcare, this is the perfect opportunity for you.

Serviços

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualificações

• Bachelor's degree in a scientific field; advanced degree preferred.
• Experience in project management and strong organizational skills.

Responsabilidades

• Assist in planning, execution, and monitoring of clinical trials.
• Coordinate study activities including site selection and data collection.

Conhecimentos

Project Management

Communication Skills

Organizational Skills

Multitasking

Data Interpretation

Formação académica

Bachelor's degree in a scientific or related field

Advanced degree (preferred)

Ferramentas

Planisware

Microsoft Project

Excel

Spotfire

Descrição da oferta de emprego

Overview

As an Associate Project Manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials, contributing to the design, analysis, and advancement of treatments and therapies.

Responsibilities

What you will be doing:

• Assisting project managers in the planning, execution, and monitoring of clinical trials.
• Understanding and interpreting data to support decision-making and problem-solving, with guidance from senior colleagues. Responsibilities include developing detailed schedules for R&D and Medical Projects across all phases, recommending improvements to enhance planning efficiency, and ensuring data quality by adhering to business rules and standards.
• Coordinating study activities, including site selection, patient recruitment, and data collection.
• Supporting the development of study protocols, case report forms, and other study-related documents.
• Participating in data analysis and interpretation to support decision-making and regulatory submissions.
• Collaborating with cross-functional teams to ensure project milestones are met and deliverables are achieved.
• Selecting suitable Work Packages within the planning system, building schedules to forecast Total Project Cost (TPC), and aligning schedules with the project strategy. Additionally, contributing to scenario planning, recommending plan adjustments, and generating status reports on project performance and quality.

Qualifications

You are:

• Bachelor's degree in a scientific or related field; advanced degree preferred.
• Advanced level of English.
• Experience in project management.
• Strong organizational and multitasking skills.
• Excellent communication and interpersonal skills.
• Ability to work effectively in a fast-paced and team-oriented environment.

Additional requirements:

• Experience with Planisware, Microsoft Project, Excel, and Spotfire.
• PMP certification (preferred).
• Experience in headcount resource and financial forecasting (preferred).

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family. Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organization. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.