Alameda, CA · On-site
$125K - $160K/yr
General Summary The Senior Clinical Budget Analyst will provide key support to the Clinical Research Department for Penumbra clinical trials and act as a core liaison between the Clinical Research ...
Alameda, CA · On-site
$125K - $160K/yr
General Summary The Senior Clinical Budget Analyst will provide key support to the Clinical Research Department for Penumbra clinical trials and act as a core liaison between the Clinical Research ...
Alameda, CA · On-site +1
$125K - $160K/yr
General Summary The Senior Clinical Budget Analyst will provide key support to the Clinical Research Department for Penumbra clinical trials and act as a core liaison between the Clinical Research ...
Alameda, CA · On-site +1
$125K - $160K/yr
General Summary The Senior Clinical Budget Analyst will provide key support to the Clinical Research Department for Penumbra clinical trials and act as a core liaison between the Clinical Research ...
... Penumbra to assess safety and effectiveness of products. This position works with confidential ... R&D, Finance, and Sales. • Attends scientific conferences and interacts with key opinion leaders.
... Penumbra to assess safety and effectiveness of products. This position works with confidential ... R&D, Finance, and Sales. • Attends scientific conferences and interacts with key opinion leaders.
Alameda, CA · On-site +1
Working in collaboration with statisticians, data managers, clinical team, CMOs, data vendors, IT ... access research activities to enhance the value proposition of Penumbra products. * Identify ...
Alameda, CA · On-site +1
Working in collaboration with statisticians, data managers, clinical team, CMOs, data vendors, IT ... access research activities to enhance the value proposition of Penumbra products. * Identify ...
Alameda, CA · On-site +1
Working in collaboration with statisticians, data managers, clinical team, CMOs, data vendors, IT ... research activities to enhance the value proposition of Penumbra products. Identify evidence gaps ...
Alameda, CA · On-site +1
Working in collaboration with statisticians, data managers, clinical team, CMOs, data vendors, IT ... research activities to enhance the value proposition of Penumbra products. Identify evidence gaps ...
... research activities to enhance the value proposition of Penumbra products. • Identify evidence ... Clinical data management systems, electronic data capture, query tools, web browser, MS Office ...
... research activities to enhance the value proposition of Penumbra products. • Identify evidence ... Clinical data management systems, electronic data capture, query tools, web browser, MS Office ...
$63K - $79.30K/yr
Penumbra's Medical Education team designs and delivers innovative programs that equip healthcare ... clinical objectives. The Sr. Medical Education Program Specialist must ensure all programs and ...
$63K - $79.30K/yr
Penumbra's Medical Education team designs and delivers innovative programs that equip healthcare ... clinical objectives. The Sr. Medical Education Program Specialist must ensure all programs and ...
... Clinical Research Organization (CRO)), or an equivalent combination of relevant education and ... Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on ...
... Clinical Research Organization (CRO)), or an equivalent combination of relevant education and ... Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on ...
What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?
What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?
What are Clinical Research Associates?
Is it hard to get a CRA job?
What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?
| Aspect | Clinical Research Associate | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often with clinical research certifications | Bachelor's degree, often with clinical research or healthcare certifications |
| Work Environment | Monitors clinical sites, reviews data, ensures compliance | Coordinates trial activities, manages schedules, and communicates with sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, CROs |
Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.
Do workers at Penumbra get paid breaks?
Does Penumbra pay people when they’re sick?
At Penumbra, are sick days and vacation days separate paid time off?
Is the health insurance from Penumbra affordable enough for their workers?
Do people get paid time off at Penumbra?
Do workers at Penumbra worry about hours?
Do Penumbra workers get to choose the shifts they work?
How easy is it to get time off at Penumbra?
Do Penumbra managers change schedules at the last minute?
Do workers at Penumbra do extra work that they don't get paid for?
How easy is it to take sick days at Penumbra?
Do people at Penumbra feel treated with respect by their managers?
Do people at Penumbra get to take their breaks without interruption?
Is it stressful to work at Penumbra?
Do people at Penumbra enjoy their jobs?
Do people at Penumbra recommend working with their team?
Do people get enough training when they start at Penumbra?
Do people get support to advance at Penumbra?
Do people think Penumbra’s headquarters understands what’s happening where they work?
Do workers feel well informed about how Penumbra is doing?
$125K - $160K/yr
Other
Medical, Dental, Vision, Life, Retirement, PTO
Posted 20 days ago
8.3
Based on 27 frontline employees who took The Breakroom Quiz
General Summary
The Senior Clinical Budget Analyst will provide key support to the Clinical Research Department for Penumbra clinical trials and act as a core liaison between the Clinical Research and Legal Departments within Penumbra.
Specific Duties and Responsibilities
Lead the process of clinical study budget negotiations with the clinical study sites (e.g., hospitals) for multiple clinical studies. *
Develop, review, and negotiate budgets and amendments for clinical trial sites.
Serve as a primary point of contact between the Clinical Research and Legal teams by submitting contract requests for clinical and investigator-sponsored studies and coordinating with all parties until finalization.
Provide management with regular updates on site start-up progress and strategic implications.
Identify and communicate any potential or actual delays, recommending solutions to keep projects on schedule.
Maintain ongoing communication with clinical project managers and study teams to provide timely status updates
Proactively identifies potential issues that may arise with budget and contract negotiations and proposes potential solutions or options*
Provide training and support for complex budget topics to junior team members
Identify and participate in ongoing process improvement initiatives when appropriate (i.e., new templates/processes, etc.)
Enter dates and comments for budget and contract in Clinical Trial Management System (CTMS) in a timely manner
Partner closely with the 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, business, finance, legal, or related field with 8+ years of clinical budget or similar relevant experience, or equivalent combination of education and experience
Additional qualifications:
Clinical research experience in a medical device, pharmaceutical or comparable regulated environment desirable but not essential
Strong organizational skills
Experience in creating and negotiating budgets
Familiarity with clinical trial agreements (contracts)
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%
Potential exposure to blood-borne pathogens
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: $125,000 - $160,000
This is the pay range for a high-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.
