| Location: |
Minneapolis, MN |
| Territory
Covered: |
Home Office Based (MN) |
| Specialty: |
| Clinical Research- Medical Device/Oncology |
|
| Description: |
Primary Responsibilities
• Handle all duties related to the execution of a Clinical Development Program from protocol design to the final clinical study report for one or several studies
• Coordinate all efforts for the trial both within the organization and through outside vendors
• Manage cross-functional project teams to deliver a high-quality clinical trial or suite of clinical trials
• Drive all aspects of the project management process from initiation, planning, execution, control to closure
• Plan/direct timelines as well as create and manage project budgets
• Deliver projects on time and within budget
• Work with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects
• Create and maintain timelines for each project, using these timelines to track and manage project progress
• Manage and coordinate all vendors involved in the clinical trials, e.g. central lab, CROs, including managing the RFP processes for each |
| Job
Requirements: |
• Bachelors degree in Life Sciences or a related field (Masters preferred)
• 3-5 years of experience in clinical project management
• Experience in oncology and medical device trials
• Experience in resource and budget/financial management
• Knowledge of clinical study guidelines (FDA, ICH and GCP)
• In-depth understanding of the clinical trials process
• Excellent communication (written and oral) and vendor-management skills
• Proven leadership, organizational, and interpersonal skills
• Willingness to travel as required |
| Compensation: |
Compensation package includes competitive salary commensurate with experience and bonus potential. |
| Benefits: |
Medical and Dental |
| Travel
Requirements: |
10-20% |
|
|
