| Job Posting Title: |
Senior Clinical Program Manager - Cardiovascular |
| Requisition Number: |
3637 |
| Country: |
US
|
| State: |
California
|
| Job Location: |
Palo Alto
|
| Functional Area: |
CLINICAL
|
| Position Type: |
Regular
|
| Full-Time / Part-Time: |
Full-Time
|
| Shift: |
Days
|
| Specific Responsibilities: |
This position reports into the Palo Alto campus supporting the Cardiovascular Franchise. |
| Essential Duties and Job Functions: |
Must meet all requirements for Clinical Program Manager position and have demonstrated proficiency in all relevant areas. Provides leadership and therapeutic expertise for the successful management of international clinical trials. Participates in development of SOPs, Clinical Study Reports, INDs, NDAs, and other clinical, regulatory, safety documents. Contributes to development of abstracts, presentations, and manuscripts. Contributes to the strategic implementation of a clinical development program(s). Provides input into the management of the Clinical Trials Management department. Recruit, hire, mentor, and manage CPA/CRA/CPA direct reports and support their professional development. Solves problems and uses judgment referring to national and international regulations, guidelines, investigator interactions and timelines. Manages international clinical trials within designated program budgets and timelines. Initiates and participates in leading departmental or interdepartmental strategic initiatives. |
| Knowledge, Experience and Skills: |
Typical requires a BS or BA in a relevant scientific discipline and minimum 10 years relevant clinical experience in the pharmaceutical industry. Extensive experience in given therapeutic area is required. Excellent interpersonal skills, ability to lead multifunctional teams, ability to manage staff, and mentor junior staff is required. Effectively solves problems and uses judgment relating to national and international regulations, guidelines, investigator interactions and timelines. Must possess a proven ability to successfully develop, implement, manage and complete clinical trials and manage vendor relations. Extensive experience in developing RFPs, selection of CROs/vendors, and management of external resources is required. Demonstrated ability to manage international clinical trials within designated program budgets and timelines is required. Must possess a proven ability to effectively communicate scientific, medical, and organizational concepts to internal and external customers. Ability to initiate, participate in and/or lead departmental or interdepartmental strategic initiatives. |
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