THERAPEUTIC EXPERIENCE REQUIRED: CNS/NEUROSCIENCE

Location: While this role is remote/home based, 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.

YOUR EXPERIENCE

• 4+ years’ Clinical Project Management (demonstrating expertise within CNS/Neuroscience) required within a CRO setting is preferred
• experience required within a CRO setting is preferred
• University/College degree, within Life Science is preferred
• Thorough knowledge of project management processes with a solid understanding of how to craft and manage a project budge
• 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 www.worldwide.com/careers! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
  

  LI-CS1 #LI-Remote

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 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. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.

WHAT YOU WILL DO

• Project Manager (PM) 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
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• thus securing the successful completion of clinical trials.

• Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented.
• Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations
• The PM, 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.

RESPONSIBILITIES

Tasks may include but are not limited to:

• Lead core project team members and facilitate their ability to lead extended/complete project team
• Lead cross unit coordination both internal and external, inclusive of sub-contractors
• Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
• Ensure successful design, implementation, tracking and revision of project plans for assigned projects
• Promote effective teamwork among project team members; resolve conflicts as needed
• Ensure appropriate communication on project-related matters with the PM Management
• Meet financial performance targets for the assigned clinical projects
• Ensure project deliverables are met according to both Worldwide and client expectations
• Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects
• Act as key client contact for assigned projects
• Establish excellent working relationships with client project teams to ensure client satisfaction and operational excellence
• Ensure that all staff allocated to assigned projects are trained on the study protocol and all other study related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations
• Liaise with functional line management in identification of any training or development needs and input into the performance appraisal process for trial team members
• Manage delegated aspects of designated projects
• Perform other duties as assigned by management

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