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| Job Title: |
Project Manager - Oncology |
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Job Location:
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Austin - Texas - USA |
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Job Category:
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Project Management
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Job description:
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POSITION SUMMARY: Ensures the contracted services and expectations of a clinical study are carried out by the CRO project team in accordance to the executed contract and the Customer’s expectations. Works in the role of a project manager on assigned project(s), which may range from single service studies to full scope or multiple protocol projects. Duties include primary liaison with Customers, Vendors and/or Investigative Sites. May have line management responsibility for Project Management staff.
ESSENTIAL JOB FUNCTIONS:
1. Acts as a primary liaison between CRO and the Customer to ensure study launch, conduct and closeout according to the Customer’s and CRO’s contractual agreement. Ensures the study is progressing according to internal and Customer quality standards, SOPs, GCPs and ICH guidelines to fulfill all federal and local regulations.
2. Serves as the team leader for the project team. Acts as a liaison and facilitator between other operation departments within CRO and DataSpectrum for project related tasks and/or issues. Plans and projects resources required across all areas of the study. Manages projects ranging in size and complexity from single service studies to full scope or multiple protocol projects with interaction from supervisor.
3. Actively manages and mentors other Project Management staff (which may include junior level Project Managers and Project Research Associates) in general team leadership skills, project management skills, internal CRO processes, and for project specific tasks.
4. Manages the executed contract and financial aspects of assigned projects. Reviews study budgets and expenses and ensures all study related contractual and budgeting issues are upheld and performed. Oversees and tracks site payment issues as required. Alerts Finance to the need for customer invoicing.
5. Develops knowledge of current therapeutic environment and drug development trends as needed. Facilitates team training in accordance with protocol and/or project requirements including therapeutic, protocol specific, and process training.
6. Reviews protocol and draft CRFs for consistency within each document. Develops and maintains project plans for the study in accordance with CRO SOPs and work instructions.
7. Maintains effective communication with the Customer and project team through oral and written correspondence, project status reports, and monthly progress reports, and ensures adequate documentation of each communication.
8. Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing and tracking reports, and functional area plans, to appropriate team members and senior management.
9. Performs on-going review of project financial status of studies within his/her responsibility; alerts senior management to potential issues and ensures necessary corrective action is taken.
10. Independently prepares information for internal review meetings. Presents prepared information at project review meetings.
11. Oversees the regulatory document collection and submission process.
12. Networks to acquire new and/or repeat business.
13. Assists in the negotiation and contracting process with outside vendors such as laboratories, printers, drug packaging, labeling and storage, and Interactive Voice Response System companies.
14. Supports the Business Development Department by providing information on CRO capabilities, patient populations, etc. Presents company capabilities as well as project management specific responsibilities at Customer proposal defense meetings.
OTHER RESPONSIBILITIES:
1. May participate in proposal and investigator grant determination.
2. May participate in Customer proposal development.
3. May represent CRO at professional meetings or seminars.
4. Performs other work-related duties as assigned.
5. Minimal travel may be required (up to 25%).
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Skills:
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Requires a B.A./B.S. in the life sciences, nursing degree, or equivalent, plus a minimum of three years clinical research experience in a contract research organization, pharmaceutical, or biotechnology company. CRO and oncology or central nervous system experience is preferred. Thorough knowledge of FDA regulations, drug development, and clinical monitoring procedures is necessary. Must have demonstrated proficiency with ICH/GCP guidelines. Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment are essential. Requires presentation, documentation and interpersonal skills as well as a team-oriented approach. Proficient computer skills in Word, Excel, PowerPoint, Email and Internet are necessary; basic computer skills using MS Project are required. |
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Employment type:
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Salary Range:
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Unspecified |
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| Other Information |
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Degree:
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Bachelors |
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Experience (year):
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3 |
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Post Date:
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09/07/2008 |
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| Contact Information |
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Address:
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<a href="http://trials.in.ua">clinical research</a> 01033 - Ukraine |
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