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
The Director, Project Management will provide support and oversight of large, multi-national projects, responsible for directing large national or global projects or a program of projects, and/or complex projects in terms of customer/deliverables, providing functional leadership to PMs. This role will work closely with Business Development and participate in Bid Defense Meetings.
Works effectively across multiple divisions to direct the delivery of projects/programs within cost, time, and quality requirements
Provide direct supervision, support, training, and mentoring to project managers
Collaborate with Business Development team on proposals and bid defense
May have immediate supervision of employees, prepares and may conduct performance appraisals and salary reviews, and applies company policies
Works with leadership in all functional areas on the continuous development/improvement of business processes to support cross-functional teams and to ensure that work is uniform, complete, and managed appropriately
Serves as a liaison with Business Development and Bids/Contracts for the client presentations and proposal development
Assists in resource utilization, policy development, and implementation of goals
What you will bring to the role
Strong leadership skills
Strong financial acumen
Expert knowledge of project management principles and application
Knowledge of budgeting, forecasting, and resource management
Skilled in process improvement, especially as it applies to clinical trials, clinical development, and project management
Extensive knowledge of various cardiovascular indications
Your experience
7-8 years industry experience with a minimum of 6 years’ experience in a Supervisory role within Clinical Project Management required (demonstrating expertise in Cardiovascular) within a CRO setting is preferred
University/College degree, within Life Science is preferred
A demonstrated track record of success in clinical development and in leading and developing professional staff in a project-led environment
Experience in developing RFPs and participating in Bid Defense Meetings
Proven experience developing and managing the budgets and resources of a segment of the business
Experience using project management software
Experience in conducting global clinical trials
Available for domestic and international travel, including overnight stays
Valid passport
Ability to drive and have a valid driver’s license
Fluent in local office language and in English, both written and verbal
Broad knowledge of drug development process and client need
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’re on a mission to hire the very best and 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.