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Sr Pm / Associate Director, Project Management - Us/Canada - Respiratory - Remote/Home Based

Company

Worldwide Clinical Trials

Address Canada
Employment type FULL_TIME
Salary
Category Biotechnology Research,Pharmaceutical Manufacturing
Expires 2023-09-27
Posted at 8 months ago
Job Description
Associate Director, Project Management
Therapeutic/Indication Experience Required: Respiratory
Location: While this role is remote/hybrid, candidates must reside the United States or Canada
Who We Are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
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 Associate Director, Project Management (ADPM) 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.
  • Works effectively across multiple divisions to direct the delivery of projects/programs within cost, time and quality requirements.
  • May have immediate supervision of employees, prepares and may conduct performance appraisals and salary reviews, and applies company policies
  • Serves as a liaison with Business Development and Bids/Contracts for the client presentations and proposal development.
  • 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.
  • Assists in resource utilization, policy development, and implementation of goals
  • Provide direct supervision, support, training and mentoring to project managers.
Responsibilities
Tasks may include but are not limited to:
  • Meet financial performance targets for the assigned clinical projects
  • Ensure that all staff allocated to assigned projects adheres to professional standards and SOPs established for clinical research
  • Define and manage project resource needs and establish contingency plans for key resources
  • Resolve conflicts as needed
  • Establish excellent working relationships with client project teams and vendors to ensure client satisfaction and operational excellence
  • May have direct reports
  • Ensure successful design, implementation, tracking and revision of project plans for assigned projects
  • Accountable for multiple projects simultaneously
  • Ensure appropriate communication on project-related matters with the PM Management
  • Ensure project deliverables are met according to both WCT and client expectations
  • Perform other duties as assigned by management Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
  • May be key client contact for assigned projects/clients
  • Lead core project team and facilitate their ability to lead extended/complete project team
  • Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects
  • Lead cross unit coordination both internal and external, inclusive of sub-contractors
  • Promote effective teamwork among project team members
What You Will Bring To The Role
  • Effective organizational skills and negotiation skills
  • Strong financial acumen
  • Knowledge of medical therapeutic area and medical terminology
  • Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
  • A relationship builder who is able to work effectively in matrix organizations
  • Excellent interpersonal skills and problem-solving ability
  • Strong leadership skills
  • A clear and deep understanding of the challenges of working in a multicultural service organization
  • Skilled in process improvement, especially as it applies to clinical trials, clinical development and project management
  • Knowledge of regulatory guidelines and Directives
  • Strong marketing and negotiation skills
  • Expert knowledge of project management principles and application
  • Excellent judgment and decision-making skills
  • Computer skills
  • Knowledge of budgeting, forecasting and resource management
Your Experience
  • Ability to drive and have a valid driver’s license
  • Experience using project management software
  • University/College degree, within Life Science is preferred
  • Fluent in local office language and in English, both written and verbal
  • Valid passport
  • A demonstrated track record of success in clinical development and in leading and developing professional staff in a project led environment
  • Broad knowledge of drug development process and client need
  • Available for domestic and international travel, including overnight stays
  • Experience in conducting global clinical trials
  • Proven experience developing and managing the budgets and resources of a segment of the business
  • 7-8 years industry experience with a minimum of 5 years’ experience in a Supervisory role within Clinical Project Management required (demonstrating expertise in Respiratory) within a CRO setting is preferred
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 www.worldwide.com/careers! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.