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Senior Director,Product Development Team Job Details

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Job Ref:  5679
State:  Maryland (MD)
City:  Gaithersburg - Corporate Headquarters
Post Code:  Dec 08, 2011
Job Description:  Position Summary:

* Overall leadership of one or more global cross-functional Product Development Teams (PDT) from candidate selection through Phase III Go decision.
* Working with project leaders and managers in Research to ensure a seamless transition of candidate biologics assets from Research to Clinical Development.
* Lead PDT to create strategic and integrated brand/product development plans which are aligned with business objectives as well as emerging project and competitive information
* Accountable for the execution of the integrated product plan to agreed scope, timelines, and resources/budget
* Accountable for ensuring that PDT outputs are cross-functionally integrated, of high quality, and strategically aligned.
* Leading/representing the PDT at governance meetings, including internal and external stakeholder management.
* Leading the PDT to effectively manage./mitigate/communicate risk, make decisions, and manage conflict and change.
* Responsible for maintaining a high degree of PDT effectiveness through collaboration, influence, and, as necessary, coaching and mentoring of team members.
* Alliance management accountabilities and responsibilities are generally consistent with those described above.
* Working with organization leadership, build systems, processes, and tools to facilitate business planning and decision making, and to grow streamlined product leadership and management capabilities.

Requirements/Qualifications:

Education: College degree in a scientific, medical, or business discipline is required. A graduate degree such as M.D., Ph.D., or PharmD is highly desired and will make the candidate most competitive.

Experience:
* 8 -- 12 years of pharma/biotech industry experience in drug development including experience in early phase non-clinical and/or clinical drug development and regulatory knowledge.
* Strong knowledge and understanding of the science of the therapeutic area
* Demonstrated ability to lead the development of project strategy and be accountable for project plans, timelines, progress, and outcomes.
* Demonstrated experience leading and motivating teams in a matrix environment.
* Demonstrated ability to cultivate excellent cross-functional collaborations
* Strong organizing and project management skills
* Demonstrated ability to effectively communicate at multiple levels of the organization.
* Demonstrated success in influencing colleagues and leaders in various departments.
* Must demonstrate high integrity.

Special Skills/Abilities: Prior experience in Oncology R&D activities. Oncology Phase I -- III drug development experience required. Prior experience with biologics is highly desirable. Experience in more than one therapeutic area as well as regulatory submissions (BLA/NDA filings) and product launches is a plus.

Requirements

Position:
* 8 -- 12 years of pharma/biotech industry experience in drug development including experience in early phase non-clinical and/or clinical drug development and regulatory knowledge.
* Strong knowledge and understanding of the science of the therapeutic area
* Demonstrated ability to lead the development of project strategy and be accountable for project plans, timelines, progress, and outcomes.
* Demonstrated experience leading and motivating teams in a matrix environment.
* Demonstrated ability to cultivate excellent cross-functional collaborations
* Strong organizing and project management skills
* Demonstrated ability to effectively communicate at multiple levels of the organization.
* Demonstrated success in influencing colleagues and leaders in various departments.
* Must demonstrate high integrity.

Education:
College degree in a scientific, medical, or business discipline is required. A graduate degree such as M.D., Ph.D., or PharmD is highly desired and will make the candidate most competitive.

MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law.

MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency.

My company shares my passion for helping to improve human health around the world.

"This is My MedImmune"

Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities... that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world.

12/08/2011
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