Director, Project Management (Rare Disease) - Remote (US)

Multiple Locations: Philadelphia, Pennsylvania, United States • Morrisville, North Carolina, United States • Boston, Massachusetts, United States • New York City, New York, United States


This position is no longer open.

Requisition Number: 1291

Position Title: Director, Project Management

External Description:

SUMMARY: The Director, Project Management (DPM) will provide functional leadership to PM/SPM, support and oversight of large, multi-national projects, may be responsible for directing and leading the activities of a therapeutic area within a Region; may be responsible for directing large national or global projects or a program of projects, and/or complex projects in terms of customer/deliverables.

Project management experience at a CRO and expertise in Rare Disease are required. Congenital adrenal hyperplasia (CAH) experience would be a bonus.

  • 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
  • Immediate supervision of employees, prepares and conducts 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 instigating and leading change initiatives
  • Communicates with sponsor (s) to obtain direction and feedback on scope of work and performance
  • 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

Tasks may include but are not limited to:

  • Direct line management of project management reports
  • Accountable for multiple projects simultaneously
  • Lead core project team 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 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 Senior Management
  • Meet financial performance targets for the assigned clinical projects/programs
  • Ensure project deliverables are met according to both WCT and client expectations
  • Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects
  • May be key client contact for assigned projects/clients
  • Establish excellent working relationships with client project teams and vendors to ensure client satisfaction and operational excellence
  • Ensure that all staff allocated to assigned projects adheres to professional standards and SOPs established for clinical research
  • 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.


  • Strong leadership skills
  • Strong financial acumen
  • Excellent judgment and decision making skills
  • Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
  • Excellent interpersonal skills and problem solving ability
  • Effective organizational skills and negotiation skills
  • Expert knowledge of project management principles and application
  • Knowledge of budgeting, forecasting and resource management
  • A relationship builder who is able to work effectively in matrix organizations
  • A clear and deep understanding of the challenges of working in a multicultural service organization
  • Knowledge of regulatory guidelines and Directives
  • Skilled in process improvement, especially as it applies to clinical trials, clinical development and project management
  • Knowledge of medical therapeutic area and medical terminology
  • Strong marketing and negotiation skills
  • Computer skills 


  • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities
  • Minimum of ten (10) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks 
  • In lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and eight (8) years clinical research experience in the pharmaceutical or CRO industries will be considered 
  • A demonstrated track record of success in clinical development and in leading and developing professional staff in a project led environment
  • 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 needs 

#LI-HH1 #LI-Remote


State: North Carolina

Employment Type: Regular

Community / Marketing Title: Director, Project Management (Rare Disease) - Remote (US)

Company Profile:

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.

Location_formattedLocationLong: Research Triangle Park, North Carolina US

CountryEEOText_Description: Worldwide Clinical Trials is an equal opportunity employer, dedicated to a policy of non-discrimination in employment on any basis including age, sex, color, race, creed, national origin, religion, marital status, sexual orientation, political belief or disability.

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