Associate Project Manager - Oncology - Canada -Remote

worldwide.com; Ottawa; Hybrid; CAD 75,000 - 90,000; Full time

Job summary

A global CRO is seeking an Associate Project Manager to coordinate and manage clinical trials with a focus on oncology studies. The ideal candidate will have at least 3 years of experience in the pharmaceutical industry, possess excellent communication and planning skills, and be proficient in MS Office and project management tools. This role offers the opportunity to work in a dynamic team environment committed to improving lives.

Qualifications

• 3 years of clinical pharmaceutical industry experience in project management.
• Experience working on oncology studies is required.
• Demonstrated ability to manage multidisciplinary project teams.

Responsibilities

• Coordinate and manage clinical trials from start to close.
• Direct technical, financial, and operational aspects of projects.
• Ensure deliverables meet customer expectations.

Skills

Project management

Communication skills

Planning and organizational skills

Ability to work independently

Proficiency in Microsoft Office

Education

University/College degree in Life Science

Tools

CTMS

EDC Systems

Job description

Associate Project Manager - Oncology - Canada -Remote page is loaded

Associate Project Manager - Oncology - Canada -Remote

Apply remote type Remote locations Virtual Canada Ontario time type Full time posted on Posted Yesterday job requisition id JR101191

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What Project Management does at Worldwide

Worldwide Clinical Trials Project management is the perfect blend of operational rigor and therapeutic expertise, with a client-focused approach. Our Global Project Leads (GPLs) and Clinical Project Managers (CPMs) expertly guide our project teams to deliver with high quality, focusing on “doing it right the first time”.

The Project Management team is engaged in all aspects of the trial collaborating with scientific and therapeutic leadership, coordinating across project teams, and providing flexible, innovative, and proactive solutions. At Worldwide, you will be dedicated to a specific therapeutic area which will not only give you an opportunity to develop in-depth global operational expertise, but also benefit from exceptional scientific and medical background that our experts bring.

What you will do

• Senior Project Manager (SPM) is responsible for the overall coordination and management of clinical trials from start-up through closeout activities.

• Directs the technical, financial, and operational aspects of the projects -- thus securing the successful completion of clinical trials.

• Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, make good business decisions, and ensure solutions are implemented.

• Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations

• The SPM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.

What you will bring to the role

• Ability to manage projects in a multi-office environment

• Excellent interpersonal, oral, and written communication skills in English

• Superior planning and organizational skills with attention to details

• Ability to work with little or no supervision

• Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

• 3 years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks

• University/College degree, within Life Science is preferred

• Experience working onOncologystudiesis required

• Can demonstrate experience of successfully managing and/or leading multidisciplinary project teams

• Ability to travel when needed

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We’reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

About Us

This is who we are.

We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever.

We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.

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