- Location:
- Gaithersburg, MD 20878
- Status:
- Full Time, Employee
- Job Category:
- Biotech/R&D/Science
Clinical Program Manager/Sr. Manager
Title: Clinical Program Manager/Sr. Manager
Location: MD Gaithersburg - Corporate Headquarters
Req: 01994
Position Summary:
Major Duties and Responsibilities:
o Lead operational activities for multiple trials
o Lead multiple cross functional project teams
o Manage all CRO activity for assigned trials
o Plan and lead Investigator Meetings
o Forecast and manage Clinical Trial budgets
o Responsible for Clinical Trial timelines
o Lead data review process for CPM team
o Lead process improvement initiatives
o Review and approves protocol and template Informed Consent Forms
Special Skills/Abilities:
o Focuses on team interaction and cooperation rather than individual heroics
o Represents the organization as the prime technical contact on contracts and projects
o Chooses one's own behaviors and responses carefully based on awareness of how it impacts others and their performance
o Interacts effectively with senior individuals outside of working group
o Frequent inter-organizational and outside contacts
o Represents the organization in providing solutions to difficult technical issues associated with specific projects
Job Complexity:
o Provide technical solutions to a wide range of difficult problems
o Solutions are imaginative thorough practicable and consistent with organizational objectives
o Contributes to the completion of specific programs and projects
o Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources
Supervision:
o Works under only general direction.
o Independently determines and develops approach to solutions
o Work is reviewed upon completion for adequacy in meeting objectives
Educations:
Requirements/Qualifications:
Education:
o BA/BS + minimum 7 years or equivalent
Experience:
o Complete understanding and wide application of technical principle theories and concepts in the field.
o General knowledge of other related disciplines.
o Specific knowledge of data collection and review
o Specific knowledge of specimen and lab collection regulatory processes compliance and IVR
o Thorough comprehension of assigned
CLICK HERE TO APPLY
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.
Location: MD Gaithersburg - Corporate Headquarters
Req: 01994
Position Summary:
Major Duties and Responsibilities:
o Lead operational activities for multiple trials
o Lead multiple cross functional project teams
o Manage all CRO activity for assigned trials
o Plan and lead Investigator Meetings
o Forecast and manage Clinical Trial budgets
o Responsible for Clinical Trial timelines
o Lead data review process for CPM team
o Lead process improvement initiatives
o Review and approves protocol and template Informed Consent Forms
Special Skills/Abilities:
o Focuses on team interaction and cooperation rather than individual heroics
o Represents the organization as the prime technical contact on contracts and projects
o Chooses one's own behaviors and responses carefully based on awareness of how it impacts others and their performance
o Interacts effectively with senior individuals outside of working group
o Frequent inter-organizational and outside contacts
o Represents the organization in providing solutions to difficult technical issues associated with specific projects
Job Complexity:
o Provide technical solutions to a wide range of difficult problems
o Solutions are imaginative thorough practicable and consistent with organizational objectives
o Contributes to the completion of specific programs and projects
o Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources
Supervision:
o Works under only general direction.
o Independently determines and develops approach to solutions
o Work is reviewed upon completion for adequacy in meeting objectives
Educations:
Requirements/Qualifications:
Education:
o BA/BS + minimum 7 years or equivalent
Experience:
o Complete understanding and wide application of technical principle theories and concepts in the field.
o General knowledge of other related disciplines.
o Specific knowledge of data collection and review
o Specific knowledge of specimen and lab collection regulatory processes compliance and IVR
o Thorough comprehension of assigned
CLICK HERE TO APPLY
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.
