Mon-Fri 40 hrs. work weekDeliverables to be performed: · Establish Dossier Plans for the assigned global submission types as needed to support the lifecycle of one or more products. · Generate ...
Quick apply
Mon-Fri 40 hrs. work weekDeliverables to be performed: · Establish Dossier Plans for the assigned global submission types as needed to support the lifecycle of one or more products. · Generate ...
Quick apply
Mon-Fri 40 hrs. work weekDeliverables to be performed: · Establish Dossier Plans for the assigned global submission types as needed to support the lifecycle of one or more products. · Generate ...
... Dossier Plans for the assigned global submission types as needed to support the lifecycle of one or more products. · Generate dossier plans that will reflect inputs from functional area ...
Quick apply
... Dossier Plans for the assigned global submission types as needed to support the lifecycle of one or more products. · Generate dossier plans that will reflect inputs from functional area ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Pleasanton, CA · On-site
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. * Interacts with regulatory affairs and ...
Pleasanton, CA · On-site
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. * Interacts with regulatory affairs and ...
Pleasanton, CA · On-site
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. * Interacts with regulatory affairs and ...
Pleasanton, CA · On-site
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. * Interacts with regulatory affairs and ...
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. Interacts with regulatory affairs and ...
$86K - $102K/yr
Contributes to the development and implementation of dossier publishing processes and procedures to improve efficiency and meet health authority standards. Interacts with regulatory affairs and ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
South San Francisco, CA · On-site
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
South San Francisco, CA · On-site
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
Letters will be reviewed and included as part of the appointment dossier of the selected candidate Apply link: HS Associate Professor Position title: Health Sciences Associate Clinical Professor ...
Letters will be reviewed and included as part of the appointment dossier of the selected candidate Apply link: HS Associate Professor Position title: Health Sciences Associate Clinical Professor ...
Redwood City, CA · On-site
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Redwood City, CA · On-site
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
South San Francisco, CA · On-site
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
South San Francisco, CA · On-site
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
$180K - $237K/yr
Oversee the end-to-end CMC dossier preparation, review, and finalization, ensuring scientific soundness, data integrity, and regulatory compliance across all product modalities. * Develop and ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Redwood City, CA · Hybrid
$183K - $242K/yr
They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational ...
Vos missions contacter les victimes, leurs ayants droit ou leurs mandataires en vue de la constitution de leur dossier (justificatifs des prejudices, remise des documents reglementaires, etc.), les ...
Vos missions contacter les victimes, leurs ayants droit ou leurs mandataires en vue de la constitution de leur dossier (justificatifs des prejudices, remise des documents reglementaires, etc.), les ...
Foster City, CA · On-site
Knowledge of Veeva RIM modules like Document Management, Registration Management, xEVMPD , Dossier Management , Application , Submission etc are required. Knowledge on other Vault like Vault eTMF ...
Foster City, CA · On-site
Knowledge of Veeva RIM modules like Document Management, Registration Management, xEVMPD , Dossier Management , Application , Submission etc are required. Knowledge on other Vault like Vault eTMF ...
Foster City, CA · On-site
Knowledge of Veeva RIM modules like Document Management, Registration Management, xEVMPD , Dossier Management , Application , Submission etc are required. Knowledge on other Vault like Vault eTMF ...
Foster City, CA · On-site
Knowledge of Veeva RIM modules like Document Management, Registration Management, xEVMPD , Dossier Management , Application , Submission etc are required. Knowledge on other Vault like Vault eTMF ...
| Aspect | Dossier | Case Manager |
|---|---|---|
| Required Credentials | Typically requires a high school diploma or equivalent; some roles may need certifications in record management | Requires a bachelor's degree in social work, healthcare, or related fields; certifications may be preferred |
| Work Environment | Office settings, record storage facilities, administrative environments | Healthcare facilities, social service agencies, client-facing settings |
| Employer & Industry Usage | Used mainly in legal, administrative, and record-keeping contexts | Common in healthcare, social services, and community support industries |
While both roles involve managing information, a Dossier focuses on organizing and maintaining records, whereas a Case Manager actively coordinates services and supports clients' needs. Understanding these differences helps in choosing the right career path or job search focus.
For Dossier jobs in California, the most frequently searched job titles are:
The top searched job categories for Dossier jobs in California are:

Contractor
Re-posted 5 days ago
Sourced by ZipRecruiter
Sapta Global is headquartered in Woodbridge, New Jersey. We are a women owned, SBA 8(a) certified company with innovative Consulting Solutions and Services firm that is dedicated to helping companies realize improved outcomes from the investments they’ve made in their Associates, Systems and Business Processes. Sapta’s expertise in professional recruitment consultancies, specializing in the placement of candidates in permanent, contract, temporary and interim positions with clients around the world. We concentrate on our customer’s key business differentiators then match relevant solutions and services that help extend the company’s value in the market. Through our unique Global delivery model and innovative design approach, we provide high value Information Services that enable our clients to enhance their business performance and increase their productivity. Our Technology advantage is the process design expertise we use from the start of our work that integrates our customer’s Strategy with their business goals. Our project management skills, software engineering practices that are integrated with software quality assurance methodologies delivers innovative solutions that provides our customers a competitive advantage.
1,001 - 5,000 Employees
Woodbridge, NJ, US
2003