Job Description
H
Headway
Licensed Psychiatrist
Headway • Alameda, CA, United States • via HospxCare - HC Employ Zone
22 hours ago
Contractor
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Job highlights
Identified by Google from the original job post
Qualifications
You’re a fully licensed psychiatrist with your DEA or CDS number, ANCC board certification, a valid NPI number and malpractice insurance
You’re looking to start or expand your private practice while maintaining control over your schedule, client load, and work environment
We accept the following licenses on a state by state basis: MD / DO
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Benefits
Wage: Up to $224/hour
Headway is here to help you start accepting insurance with ease, increase your earnings with higher rates, and start taking covered clients sooner
Hassle-free insurance credentialing: Get credentialed for free in multiple states within as little as 30 days
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Responsibilities
This position is for licensed psychiatrists looking to build or grow their private practice
Headway provides the tools, resources, and support to help you navigate insurance, streamline operations, and focus on delivering quality care - on your own terms
Instant verification: Clients can easily check their insurance status and get the care they need without disruption
Job description
"
Licensed Psychiatrist
Wage: Up to $224/hour
Licensed psychiatrist - Are you ready to launch or expand your private practice? Headway is here to help you start accepting insurance with ease, increase your earnings with higher rates, and start taking covered clients sooner. It’s all on one free-to-use platform, no commitment required.
About the role
This position is for licensed psychiatrists ...
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Abbott Laboratories
Senior Specialist Regulatory Affairs
Abbott Laboratories • Alameda, CA, United States • via Abbott Jobs
7 hours ago
Full–time
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Job highlights
Identified by Google from the original job post
Qualifications
Bachelors Degree (± 16 years), Related field OR an equivalent combination of education and work experience
Minimum 3 years, 3-4 years experience in a regulated industry (e.g., medical products, nutritionals)
Regulatory history, guidelines, policies, standards, practices, requirements and precedents
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Benefits
Career development with an international company where you can grow the career you dream of
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
An excellent retirement savings plan with high employer contribution
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Responsibilities
As an individual contributor in the function of a Sr. Regulatory Affairs Specialist, you will provide support to the Regulatory Affairs department to ensure efficient and compliant business processes and environment are followed
With limited supervision you will execute tasks and partner across business functions
The individual will be reviewing Labeling, Advertising and Promotional materials, determining risk, identifying data needed, obtaining data, and ensuring that the information is reliable and effectively presented to substantiate claims
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Job description
Job Description
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
• Career development with an international company where you can grow the career you dream of
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists
We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.
The Opportunity
This Senior Regulatory Affairs Specialist will work out of our Alameda, CA location in the Diabetes Care Division. As an individual contributor in the function of a Sr. Regulatory Affairs Specialist, you will provide support to the Regulatory Affairs department to ensure efficient and compliant business processes and environment are followed. With limited supervision you will execute tasks and partner across business functions.
The individual will be reviewing Labeling, Advertising and Promotional materials, determining risk, identifying data needed, obtaining data, and ensuring that the information is reliable and effectively presented to substantiate claims. You may also have opportunities to participate in worldwide regulatory submissions.
This is a broad scoped position with strong opportunity for growth and career development based on performance.
As an individual contributor, the Senior Regulatory Affairs Specialist will support product development and regulatory activities to commercialize new digital products and features including generative AI technologies designed to help millions of patients in the US. In this role, you will provide regulatory input on design and development activities to cross-functional teams, including software development and systems engineering members, and ensure availability of documentation to support submission activities to meet program objectives and timelines. Prior experience working with software development teams, diabetes management devices (e.g. insulin dosing algorithms), and artificial intelligence/machine learning technologies is preferred. This role will also be an important resource for the regulatory department to ensure efficient and compliant business processes. This is an exciting opportunity to work in the dynamic and evolving digital health space.
What You’ll Work On
• Review and analyze labeling, advertising and promotional materials while working with Marketing teams to provide regulatory strategy and compliance input.
• Coordinate RA Ad & Promo activities among internal Regulatory functions and Division cross functional teams. Facilitate development and process discussions toward implementing advertising and promotion improvement processes.
• Support RA Ad & Promo management ensuring on time department deliverables and developing mitigation plans for any issues that are identified, including Ad & Promo process improvements.
• Analyze reports and metrics from tracking tools, identifying trends and ramifications.
• Lead and execute projects that support the strategic direction of Division, working independently or as part of a team.
• Lead and support projects involving AI-driven solutions, ensuring successful implementation and integration into business processes.
• Lead junior RA Ad & Promo team members, developing their skills/abilities, verifying work, and assisting them in areas of efficiency and regulatory knowledge.
• Function as a team lead when RA Management is not available toward prioritizing department workstream and facilitating issue resolution or escalation.
• Assist with activities related to NPI and on market products (510K, PMA, Health Canada submissions and Latin America countries) as needed.
• Determine and communicate promotional content and approval requirements to cross functional teams with limited supervision.
• Assist compliance with product post-marketing approval requirements as needed.
Required Qualifications
• Bachelors Degree (± 16 years), Related field OR an equivalent combination of education and work experience
• Masters Degree (± 18 years), In Regulatory Affairs preferred and may be used in lieu of direct regulatory experience.Minimum 3 years, 3-4 years experience in a regulated industry (e.g., medical products, nutritionals). 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)
• Knowledge of:
Regulatory history, guidelines, policies, standards, practices, requirements and precedents.
