She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance ...
She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance ...
She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance ...
She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance ...
Regulatory Analyst
Signal Hill, CA · On-site
Regulatory Submissions Management and Operations for Janssen R&D Project Goal (Mandatory): The management and delivery of regulatory submissions to global health authorities required to support the ...
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Regulatory Analyst
Signal Hill, CA · On-site
Regulatory Submissions Management and Operations for Janssen R&D Project Goal (Mandatory): The management and delivery of regulatory submissions to global health authorities required to support the ...
Manager, Regulatory Operations and Publishing
San Diego, CA · Remote
$134K - $162K/yr
Manage submission execution activities, including deliverable tracking, timeline coordination, submission readiness assessments, and communication with Regulatory Affairs and cross-functional ...
Manager, Regulatory Operations and Publishing
San Diego, CA · Remote
$134K - $162K/yr
Manage submission execution activities, including deliverable tracking, timeline coordination, submission readiness assessments, and communication with Regulatory Affairs and cross-functional ...
Manager, Regulatory Operations and Publishing
San Diego, CA · Remote
$134K - $162K/yr
Generate submission-ready PDFs in compliance with regulatory guidance, eCTD requirements, and internal PDF publishing standards. * Perform technical QC of submission documents and published ...
Manager, Regulatory Operations and Publishing
San Diego, CA · Remote
$134K - $162K/yr
Generate submission-ready PDFs in compliance with regulatory guidance, eCTD requirements, and internal PDF publishing standards. * Perform technical QC of submission documents and published ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
Resume Submission
Los Angeles, CA · On-site
About Us Everchron is a legal tech company built by lawyers for lawyers. We build cloud-based case management software for top tier law firms and Fortune 500 companies so that their lawyers can ...
Resume Submission
Los Angeles, CA · On-site
About Us Everchron is a legal tech company built by lawyers for lawyers. We build cloud-based case management software for top tier law firms and Fortune 500 companies so that their lawyers can ...
General Submission
Manhattan Beach, CA · On-site
Pearl Abyss America, Inc . - the team behind Black Desert and Crimson Desert as well as the upcoming titles DokeV and Plan8- is seeking a high-performing, creative, results-oriented, and quality ...
General Submission
Manhattan Beach, CA · On-site
Pearl Abyss America, Inc . - the team behind Black Desert and Crimson Desert as well as the upcoming titles DokeV and Plan8- is seeking a high-performing, creative, results-oriented, and quality ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
General Submission
Santa Rosa, CA · On-site
$21 - $22/hr
General SubmissionPlease feel free to drop off your resume for review if we do not have an open listing. We review these resumes often for upcoming roles! Job Posted by ApplicantPro
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General Submission
Santa Rosa, CA · On-site
$21 - $22/hr
General SubmissionPlease feel free to drop off your resume for review if we do not have an open listing. We review these resumes often for upcoming roles! Job Posted by ApplicantPro
General Submission
Manhattan Beach, CA · On-site
Pearl Abyss America, Inc . - the team behind Black Desert and Crimson Desert as well as the upcoming titles DokeV and Plan8- is seeking a high-performing, creative, results-oriented, and quality ...
General Submission
Manhattan Beach, CA · On-site
Pearl Abyss America, Inc . - the team behind Black Desert and Crimson Desert as well as the upcoming titles DokeV and Plan8- is seeking a high-performing, creative, results-oriented, and quality ...
Principal Regulatory Affairs Specialist
Irvine, CA · On-site
$127K - $153K/yr
Ensure submissions are scientifically sound, technically accurate, well organized, and compliant with applicable regulations, standards, and guidance documents. * Support regulatory agency ...
Principal Regulatory Affairs Specialist
Irvine, CA · On-site
$127K - $153K/yr
Ensure submissions are scientifically sound, technically accurate, well organized, and compliant with applicable regulations, standards, and guidance documents. * Support regulatory agency ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
Resume Submission
Palo Alto, CA · On-site
If you do not see a position(s) currently listed that matches your experience, you can still submit your resume-- we'd love to hear from you! PsiQuantum provides equal employment opportunity for all ...
Principal Regulatory Affairs Specialist
Irvine, CA · On-site
$127K - $153K/yr
Ensure submissions are scientifically sound, technically accurate, well organized, and compliant with applicable regulations, standards, and guidance documents. Support regulatory agency interactions ...
Principal Regulatory Affairs Specialist
Irvine, CA · On-site
$127K - $153K/yr
Ensure submissions are scientifically sound, technically accurate, well organized, and compliant with applicable regulations, standards, and guidance documents. Support regulatory agency interactions ...
$90 - $130/hr
C. The Rankings, Awards & Media Relations Coordinator supports the firm's strategy for awards, surveys, league tables, and legal directory submissions - including but not limited to Chambers and ...
$90 - $130/hr
C. The Rankings, Awards & Media Relations Coordinator supports the firm's strategy for awards, surveys, league tables, and legal directory submissions - including but not limited to Chambers and ...
This position supports product registrations, regulatory submissions, approvals, and post-market regulatory requirements across domestic and international markets. The Regulatory Affairs Specialist ...
This position supports product registrations, regulatory submissions, approvals, and post-market regulatory requirements across domestic and international markets. The Regulatory Affairs Specialist ...
Director, RA
San Francisco, CA · On-site
$176K - $233K/yr
Develop and implement regulatory strategies for successful submission of product candidates from pre-IND stage through the product approval process. * Collaborate with project teams to ensure ...
Quick apply
Director, RA
San Francisco, CA · On-site
$176K - $233K/yr
Develop and implement regulatory strategies for successful submission of product candidates from pre-IND stage through the product approval process. * Collaborate with project teams to ensure ...
This position supports product registrations, regulatory submissions, approvals, and post-market regulatory requirements across domestic and international markets. The Regulatory Affairs Specialist ...
Quick apply
This position supports product registrations, regulatory submissions, approvals, and post-market regulatory requirements across domestic and international markets. The Regulatory Affairs Specialist ...
S. regulatory submissions, including 510(k) submissions and other applicable premarket activities * Support international regulatory submissions and registrations across applicable global markets
S. regulatory submissions, including 510(k) submissions and other applicable premarket activities * Support international regulatory submissions and registrations across applicable global markets
Director, Regulatory Affairs
Fremont, CA · On-site
$192K - $253K/yr
Develop and implement regulatory strategies for successful submission of product candidates from pre-IND stage through the product approval process. * Collaborate with project teams to ensure ...
Quick apply
Director, Regulatory Affairs
Fremont, CA · On-site
$192K - $253K/yr
Develop and implement regulatory strategies for successful submission of product candidates from pre-IND stage through the product approval process. * Collaborate with project teams to ensure ...
Submissions information
What is a submissions role?
What are the key skills and qualifications needed to thrive as a submissions specialist?
What are some common challenges faced in a submissions role, and how can they be managed?
What is the difference between Submissions vs Data Entry Clerk?
| Aspect | Submissions | Data Entry Clerk |
|---|---|---|
| Required Credentials | Varies; often includes industry-specific certifications | High school diploma or equivalent; some roles may require basic certifications |
| Work Environment | Office, remote, or online platforms | Office settings, data centers, or remote work |
| Employer & Industry Usage | Used across various industries for submitting documents, applications, or content | Commonly employed in administrative, healthcare, and finance sectors for inputting data |
| Search & Comparison Intent | Focuses on submitting information or content | Involves entering and managing data accurately |
Submissions generally refer to the act of submitting documents, applications, or content, often requiring specific industry certifications. Data Entry Clerks focus on inputting and managing data within organizations, typically with basic qualifications. While both roles involve handling information, Submissions emphasizes the process of submitting, whereas Data Entry Clerks concentrate on data management and accuracy.
What are popular job titles related to Submissions jobs in California?
For Submissions jobs in California, the most frequently searched job titles are:
What job categories do people searching Submissions jobs in California look for?
The top searched job categories for Submissions jobs in California are:
What cities in California are hiring for Submissions jobs?
Cities in California with the most Submissions job openings:

Other
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 11 days ago
Job description
SUMMARY/JOB PURPOSE:
The Associate Regulatory Operations Director is responsible for overseeing submission activity for the company's submission portfolio, with first line accountability for managing the submission forecast and ensuring proper staffing for upcoming submissions. She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance towards achieving department application filing objectives , identifying areas of concern that are impacting submission timelines, drive process efficiencies and overall operational effectiveness for timely and high-quality regulatory submissions. This role also provides oversight and guidance on the Veeva RIM suite and identify best practices for effective implementation.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
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Oversees the planning of all regulatory submissions (INDs, NDAs, BLAs, supplemental applications, etc.) in electronic format.
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Accountable for the oversight of regulatory submission processes and best practices, bringing clarity to submission timelines and deliverables.
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Works collaboratively with Regulatory Affairs and contributing cross-functional team members in order to create and maintain global regulatory submission project plans, manages deliverable timelines and activities, ensures alignment on roles and responsibilities, and that any issues, risks, or impact due to changes in strategy and/or timelines are assessed quickly throughout the submission process ensuring transparency of submission status to key stakeholders and management.
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Leads a cross-functional team within Exelixis to explore submission process optimization.
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Develops submission planning best practices and implementation of major submission timelines.
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Partners with Vice President, Regulatory Operations in the development and implementation of Department best practices and ways of working.
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Provides key insight to identify IT solutions to enhance Regulatory Operations systems (i.e., Project planning tools, Veeva RIM)
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Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal guidelines) and other departmental initiatives to improve standards and systems internally.
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Mentors/instructs members of the Regulatory Operations team on Best Practices for submission planning.
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Reviews and interprets regulatory guidelines.
SUPERVISORY RESPONSIBILITIES:
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None.
EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education/Experience:
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Bachelor's degree in related discipline and a minimum of eleven years of related experience; or,
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Master's degree in related discipline and a minimum of nine years of related experience; or,
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PhD degree in related discipline and a minimum of five years of related experience; or,
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Equivalent combination of education and experience.
Experience/The Ideal for Successful Entry into Job:
Knowledge/Skills:
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Develops and manages plans within established timelines and balances commitments to complete multiple activities and achieve results. Takes pride in delivering high quality work.
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Applies wide knowledge of the regulatory framework and industry practices to develop innovative approaches and complete complex work.
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Demonstrates clear and effective verbal and written communication. Provides timely and appropriate information updates. Speaks clearly and confidently in one-to-one situations and effectively presents information to groups of departmental colleagues.
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Strong interpersonal skills and ability to accommodate differing views to actively support the development of an agreed upon resolution.
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Manages effectively performing teams to achieve common objectives. Engages internal stakeholders to establish productive collaborative relationships.
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Applies knowledge of organizational goals and objectives and demonstrates skill and insight in gathering, analyzing and applying key information to solve problems.
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Leads self and others; acts with integrity and builds trust with colleagues to contribute to accomplishing team objectives.
JOB COMPLEXITY:
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Capable of managing the execution of multiple tasks.
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Ensures appropriate prioritization and execution for area of responsibility.
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Proactively anticipates, prioritizes and resolves task-related challenges.
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Designs and implements solutions to address task-related challenges, taking into consideration the broader impact.
WORKING CONDITIONS:
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Travel approximately 20%
DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state, or local protected class.
#LI-MB1
Our compensation reflects the cost of labor across severalU.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this positionis $157,500 - $222,500 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors. In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.If you have a disability and need an accommodation in relation to the recruiting process, please email us at: ApplicantAccommodations@exelixis.com.
WORKING CONDITIONS:
Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.
DISCLAIMER:
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
About Exelixis
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
501 - 1,000 Employees
Headquarters location
Alameda, CA, US
Year founded
1994