San Diego, CALIFORNIA | about 1 month
$85,583 Average salary of similar jobs | Check Salary...
|Director, Project Management|
|The Senior Project Manager (SPM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. WCT Project Managers are 100% accountable for the success of their projects:|
SPM is responsible for the overall coordination and management of clinical trials from start up through close out 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.
Tasks may include but are not limited to:
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 the PM Management
Meet financial performance targets for the assigned clinical projects
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
Act as key client contact for assigned projects
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.
Manage all aspects of designated projects
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.
OTHER SKILLS AND ABILITIES:
The SPM possesses a high level of the following skills and attributes
Sound knowledge of the key principles of cross functional project management (time, quality, cost)
Solid financial acumen
Effective negotiation technique and evidence of commercial and organizational knowledge
Displays effective communication skills (listening, oral and written) and can communicate in the English language (oral and written)
The ability to persuade, convince, and influence/impress others
Organizational skills and proficiency at multi-tasking with good attention to detail
Demonstrated ability to lead, motivate and coordinate teams and coach/mentor team members as appropriate
The ability to delegate effectively and prioritise own and workload of project team members
Cross cultural awareness and ability to adapt appropriately
Ability to work independently
Good 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 seven (7) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
o In lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and six (6) years clinical research experience in the pharmaceutical or CRO industries will be considered
Thorough knowledge of project management processes
Can demonstrate experience of successfully managing and/or leading multidisciplinary project teams
Experience using project management software
Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
Solid understanding of how to craft and manage a project budget
Available for domestic and international travel, including overnight stays
Valid current passport required
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
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