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Section: Defence/Armed Forces Vacancy 1137 |
Post:Drug Development Project Manager – preclinical small molecule programs |
Salary contractual |
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Requirements and conditions |
Age: |
Has no value
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Gender |
Has no value
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Education: |
no
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Work schedule: |
Has no value
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Work place: |
London
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The announcement text: |
Company:
Stemline Therapeutics, Inc.
Company description:
Stemline is a clinical stage, oncology-focused biopharmaceutical company developing drug candidates that target cancer stem cells. The Company has built a broad pipeline of compounds which include both biologics and small molecules, a robust discovery platform, and a comprehensive intellectual property portfolio.
Title:
Drug Development Project Manager – preclinical small molecule programs
Job Description:
Stemline Therapeutics is currently seeking a Drug Development Project Manager who will be responsible for managing multiple preclinical small molecule programs. This Project Manager will lead and coordinate the various aspects of these programs including the project team, contract research organizations (CROs), and academic collaborators. The Project Manager will manage all aspects of the Company’s preclinical small molecule programs, including:
• Identify, negotiate with, and engage consultants and CROs to manage the medicinal chemistry, synthesis, and ADME studies to optimize the Company’s therapeutic small molecule candidates
• Work with CROs, and certain select academic laboratories, to identify and employ functional assays to validate compound activity
• Work regularly with the Company’s medicinal chemistry consultants to develop and implement a medicinal chemistry program around the Company’s small molecule candidates
• Identify, negotiate with, engage, and manage CROs to perform medicinal chemistry and synthesis of select small molecules
• Identify, negotiate with, engage, and manage CROs to perform ADME studies
• Present status updates to management via regular team meetings
• Organize and maintain accurate budgets
• Keep management informed of project status and escalating issues when they impact timeline, scope, quality or budget
• Coordinate and develop yearly project goals, strategic plans and annual project budgets and ensure integration of these goals with overall corporate objectives
• Assess project issues and areas of risk and developing mitigation plans to assist in management decision making
Qualifications:
• Requires BA/BS, MS in life sciences or business related field. PhD preferred.
• A minimum of 2 years bench work in a relevant scientific field.
• Experience with pre-clinical small molecule therapeutic development.
• 2 years experience working in a biotechnology/pharmaceutical company
Skills, Knowledge and Abilities:
• Experience with small molecule drug development
• Experience negotiating with Contract Research Organizations
• Demonstrated experience managing CROs and consultants
• Must have entrepreneurial attitude, ability to be creative thinker
• Work well independently using strong organizational, project and time management skills
• Effective communication skills, both written and verbal
Compensation: Commensurate with experience
Principals only. Recruiters, please don`t contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
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Contact information |
Employer: |
Åâãåíèé
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Email: |
info@elikaassociates.com
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Phone: |
8 (044) 593-85-63, 64
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Publication date: 2009-09-21 20:32:27
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