Clinical Budget Analyst

General Summary
As the Clinical Budget Analyst, you will provide essential support to the Clinical Research Department for Penumbra clinical trials and act as a key liaison between the Clinical Research and Legal Departments within Penumbra.
Specific Duties and Responsibilities
•    Drive the process of clinical study budget negotiations with the clinical study sites (e.g., hospitals) for multiple clinical studies. *
•    Prepare and negotiate site clinical trial budgets and budget amendments. *
•    Act as a key liaison between the Clinical Research and Legal Departments. Submit contract requests for clinical studies and investigator-sponsored studies and follow through with internal and external stakeholders to completion. *
•    Provide periodic updates to management regarding site start-up progress related to their strategic impact. Communicate potential or actual delays and propose actions to ensure that project timelines are met. *
•    Communicates regular updates to clinical project manager and other study staff.
•    Proactively identifies potential issues that may arise with budget and contract negotiations
•    Partner closely with Legal team to manage timelines and expectations for new and changing clinical studies on a regular basis. *
•    Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. *
•    Understands relevant security, privacy and compliance principles and adheres to the regulations, standards, and procedures that are applicable to the Company. *
•    Ensure other members of the department follow the QMS, regulations, standards, and procedures. *
•    Perform other work-related duties as assigned.
*Indicates an essential function of the role
 
Position Qualifications
Minimum education and experience:
•    Bachelor's degree in life sciences or related field with 5+ years of experience, or equivalent combination of education and experience

Preferred qualifications:
•    Experience in a medical device, pharmaceutical or comparable regulated environment desirable but not essential
•    Strong organizational skills and demonstrated competence in word processing and database creation and management are critical skill sets
•    Ability to process a high volume of work and meet deadlines in a fast-paced environment is essential
•    High degree of accuracy and attention to detail necessary
•    Creative problem-solving skills are highly desirable
•    Outstanding written, oral, and interpersonal communication skills are required
•    Proficiency with MS Word, Excel, and PowerPoint
•    Excellent organizational skills with ability to prioritize assignments while handling various projects simultaneously

Working Conditions
•    General office, laboratory, and cleanroom environments
•    May have business travel from 0% - 5%
•    Requires some lifting and moving of up to 15 pounds
•    Must be able to move between buildings and floors
•    Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day
•    Must be able to read, prepare emails, and produce documents and spreadsheets
•    Must be able to move within the office and access file cabinets or supplies, as needed
•    Must be able to communicate and exchange accurate information with employees at all levels on a daily basis

 

Annual Base Salary Range:  $93,000 - $130,000   
This is the pay range for a mid-cost labor market. If hired in another region, there will be a difference in pay range. We offer a competitive compensation package plus a benefits and equity program, when applicable. Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

• A collaborative teamwork environment where learning is constant, and performance is rewarded.

• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.

• A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

 

Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc.

 

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws.

 

If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents.

 

For additional information on Penumbra’s commitment to being an equal opportunity employer, please see Penumbra's AAP Policy Statement.