Associate Regulatory Affairs Submission Management
2 months ago
Duration: 1 year
Employment Type:W-2
Overview:
- The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.
- With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications.
- This individual is recognized as a very knowledgeable in their discipline expert and in regulatory affairs submission management.
Responsibilities:
- Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.
- Acts as RA Submissions support to project teams providing guidance and communication of established submission processes and standards. Provides input to project publishing timelines and deliverables.
- Participates in submission team meetings.
- Expedites, manages, and coordinates multiple
- concurrent interrelated activities for submission projects in the delivery of low to moderately complex published submissions within the required timelines.
- Anticipates obstacles and proposes solutions within the team.
- Coordinates submission publishing with offsite publishers/provides notification to ensure all required resources are available to meet submission timelines.
- Prepares content planner for publishing and works with vendor to resolve publishing issues. May perform in-house publishing tasks
- Facilitates the creation or procurement of submission content deliverables such as cover letters and forms
- Performs detailed quality reviews of published output to ensure compliance with Regulatory Standards and Health Authority guidence including verification of content, bookmarks, hypertext links and tables of content in low to moderately complex submissions.
- Facilitates team reviews.
- Contributes to the development of optimal business processes and standards within the
- department to ensure high levels of customer support and to achieve high quality submissions.
- Contributes to the implementation of internal process and standards documents relating to publishing and publishing deliverables.
- Suggests and contributes to process improvements, including changes to software and business processes.
- May participate on internal project teams to update business software.
- Demonstrates ability to influence without direct authority. Builds and maintains positive
- relationships internally and externally.
- Position accountability/scope: o Supervision required o Receives project assignments from manager but has responsibility for managing own projects with oversight o Reviews project progress with manager on a regular basis with direction provided by manager o May assist with onboarding staff.
Qualifications:
- Required Education: Bachelor’s Degree
- Required Experience: Two years pharmaceutical or industry related experience
- Preferred experience: Publishing related software tools e.g. Documentum, eCTDXPress/ISIPublisher, ISI Toolbox/DocuBridge/Insight platform, Adobe Acrobat.
Top 3-5 skills, experience:
1. eCTD submission publishing (advertising and promotional 2253 submissions if possible)
2. US regulatory FDA guidelines/CFR
3. submission/regulatory project management
4. Veeva Promomats experience
5. Lorenz publishing software experience
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Anil
Email: anil.g@ustechsolutionsinc.com
Internal Id: 24-20483
-
Regulatory Affairs Submission Manager
3 weeks ago
North Chicago, Illinois, United States US Tech Solutions Full timeJob Title: Associate Regulatory Affairs Submission ManagementAt US Tech Solutions, we are seeking a highly skilled Associate Regulatory Affairs Submission Management professional to join our team.About the Role:The Associate Regulatory Affairs Submission Management will be responsible for managing low to medium impact submission projects involving multiple...
-
North Chicago, Illinois, United States US Tech Solutions Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Submission Management Associate to join our team at US Tech Solutions.The successful candidate will be responsible for managing low to medium impact submission projects involving multiple cross-functional regulatory submission teams.Key Responsibilities:Manage submission projects from initiation...
-
Regulatory Affairs Submission Manager
1 month ago
North Chicago, Illinois, United States US Tech Solutions Full timeJob Title: Associate Regulatory Affairs Submission ManagementAbout the Role:We are seeking an experienced Associate Regulatory Affairs Submission Management professional to join our team at US Tech Solutions. As a key member of our regulatory affairs team, you will be responsible for managing low to medium impact submission projects, ensuring timely delivery...
-
Associate Regulatory Affairs Submission Management
2 months ago
North Chicago, United States US Tech Solutions Full timeDuration: 1 year Employment Type: W-2 Overview: The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines,...
-
Regulatory Affairs Submission Manager
2 weeks ago
Chicago, Illinois, United States AbbVie Full timeJob DescriptionAbbVie is seeking a highly skilled Regulatory Affairs Submission Manager to join our team. As a key member of our Regulatory Affairs department, you will be responsible for managing medium to high-impact submission projects, ensuring timely delivery of high-quality dossiers that meet regulatory authorities' technical specifications.Key...
-
Regulatory Affairs Submission Manager
1 week ago
North Chicago, Illinois, United States US Tech Solutions Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Submission Manager to join our team at US Tech Solutions. As a key member of our regulatory affairs team, you will be responsible for managing low to medium impact submission projects, ensuring timely delivery of high-quality dossiers that meet technical specifications defined by regulatory...
-
Regulatory Affairs Submission Manager
1 week ago
Chicago, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Submission Manager to join our team at AbbVie. The successful candidate will be responsible for managing medium to high-impact submission projects, ensuring timely delivery of high-quality dossiers that meet regulatory authority requirements.Key ResponsibilitiesManage submission projects,...
-
North Chicago, Illinois, United States US Tech Solutions Full timeAbout the RoleUS Tech Solutions is seeking a highly skilled Regulatory Affairs Submission Management professional to join our team. As a key member of our regulatory affairs team, you will be responsible for managing low to medium impact submission projects, ensuring timely delivery of high-quality dossiers that meet technical specifications defined by...
-
Regulatory Affairs Associate I
3 weeks ago
North Chicago, United States Collabera Full timeJob DescriptionJob Description· What are the top 3-5 skills, experience or education required for this position:· eCTD submission publishing (advertising and promotional 2253 submissions if possible)· US regulatory FDA guidelines/CFR submission/regulatory project managementAll potential applicants are...
-
Regulatory Affairs Associate I
4 weeks ago
North Chicago, United States Collabera Full timeJob DescriptionJob Description· What are the top 3-5 skills, experience or education required for this position:· eCTD submission publishing (advertising and promotional 2253 submissions if possible)· US regulatory FDA guidelines/CFR submission/regulatory project management Veeva Promomats...
-
Regulatory Affairs Associate I
2 weeks ago
Chicago, Illinois, United States Collabera Full timeJob OverviewWe are seeking a highly skilled Regulatory Affairs Associate I to join our team at Collabera. As a key member of our regulatory affairs team, you will be responsible for managing low to medium impact submission projects, ensuring timely delivery of high-quality dossiers that meet technical specifications defined by regulatory authorities.Key...
-
Senior Regulatory Affairs Specialist
3 weeks ago
North Chicago, Illinois, United States Abbott Laboratories Full timeAbout AbbottAbbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.Job SummaryWe are seeking a Senior Regulatory Affairs...
-
Senior Manager, Regulatory Affairs CMC
6 days ago
Chicago, Illinois, United States AbbVie Full timeJob DescriptionAbbVie is a leading biopharmaceutical company that discovers and delivers innovative medicines and solutions to address serious health issues. We are committed to making a remarkable impact on people's lives across various therapeutic areas, including immunology, oncology, neuroscience, and eye care.The Senior Manager, Regulatory Affairs CMC,...
-
Senior Director Global Regulatory Affairs
4 weeks ago
Chicago, Illinois, United States Danaher Corporation Full timeJob Title: Senior Director Global Regulatory AffairsAt Danaher Corporation, we are committed to accelerating the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.Job SummaryWe are seeking a highly...
-
Regulatory Affairs Manager
2 weeks ago
Chicago, Illinois, United States AbbVie Full timeJob Title: Senior Manager, Regulatory Affairs AdvertisingJob SummaryAbbVie is seeking a Senior Manager, Regulatory Affairs Advertising to join our team. This role will be responsible for ensuring that advertising and promotion materials are accurate, competitive, and compliant with internal policies and regulations.Key ResponsibilitiesDevelop and implement...
-
Senior Manager Regulatory Affairs
4 weeks ago
Chicago, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Senior Manager Regulatory Affairs to join our team at AbbVie. As a key member of our Global Regulatory Strategy team, you will be responsible for developing and implementing regulatory strategies for assigned products in the US and Canada.Key ResponsibilitiesDevelop and implement regulatory strategies for assigned...
-
Senior Manager Regulatory Affairs
2 weeks ago
Chicago, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Senior Manager Regulatory Affairs to join our team at AbbVie. As a key member of our Global Regulatory Strategy team, you will be responsible for developing and implementing regulatory strategies for assigned products or product lines.Key ResponsibilitiesDevelop and implement regulatory strategies for assigned...
-
CER Medical Writer
7 days ago
North Chicago, United States Rangam Full timeRegulatory Submission Writer Ivd or medical device or pharma experienceProofreading on the submissionauthor the submission is plusWorking with cross-functional teamRegulatory submissionProduct labellingLooking for regulatory backgroundIvdr submission, Pma, 510k submissionRegulatory submission writingRole Requirements and Expectations:The company is seeking...
-
Senior Director of Regulatory Affairs
1 week ago
Chicago, Illinois, United States Meitheal Pharmaceuticals Inc Full timeJob SummaryThe Senior Director of Regulatory Affairs will provide regulatory guidance for product development and tech transfer, especially biosimilars. This role involves preparing and reviewing submissions and working closely with cross-functional teams within the company and across business partners.Key ResponsibilitiesThoroughly understand US regulatory...
-
Regulatory Affairs Director
7 days ago
Chicago, Illinois, United States Tempus Full timeRegulatory Affairs DirectorTempus is seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our regulatory team, you will be responsible for developing and executing global regulatory strategies to support business objectives.Key Responsibilities:Develop and execute global regulatory strategies to support business...