Associate Submission Manager
3 weeks ago
Manage activities associated with the preparation of non-oncology Investigator Brochure (IB) annual updates within Biomedical Research (BR) in compliance with internal SOP and health authority requirements.
Organizing and chairing the kick-off meeting to establish the level of update and contributors across Biomedical Research Translational Medicine and Development.
Leads subsequent IB planning discussions, creating, and maintaining a comprehensive project plan capturing actions and key activities, target governance board review, content delivery timelines, and finalization date for IB.
Manage stakeholder engagement, and ensure that any issues, risks, or impact due to changes in strategy and/or timelines are assessed quickly and remediated.
Timely escalation (as per agreed process) if the IB will not be finalized within the annual update period.
Collaboration with Document Quality Management (DQM) team and other key stakeholders e.g. Regulatory Operations to ensure strategic resource planning of downstream activities allowing IB to be finalized in accordance with targeted timelines. Completion of all internal documentation and distribution of the final IB package in accordance with SOP and internal guidance.
Timely update of all internal tracking systems.
Manage submission related activities associated with the preparation of Clinical Trial Application submissions following internal working practice, guidance, and SOPs to ensure the delivery of high-quality submission documents to regulatory operations.
This may include creation of requisite templates, drafting of timelines, ensuring documents are finalized according to internal process via source data verification and formatting checks in accordance with agreed timelines, and stakeholder management.
Manage the preparation of Biomedical Research components (preclinical and early phase clinical) of supplementary submissions.
May distribute workload to and collaborate with external vendor on documentation specific activities.
Regularly maintain supporting IT systems/trackers to ensure accuracy of information by liaising with stakeholders.
-
Associate Submission Manager
1 month ago
hyderabad, India Novartis Full timeYour responsibilities include, but are not limited to:Provide operational support to the BR Submission manager with many of the tasks involved with the smooth running of regulatory submission preparation in compliance with Novartis processes. Collaborate with the SM in taking action to address issues as they arise. Ensure all assigned submission related...
-
Associate Submission Manager
3 weeks ago
Hyderabad, India Novartis Full timeManage activities associated with the preparation of non-oncology Investigator Brochure (IB) annual updates within Biomedical Research (BR) in compliance with internal SOP and health authority requirements.Organizing and chairing the kick-off meeting to establish the level of update and contributors across Biomedical Research Translational Medicine and...
-
Associate Submission Manager
3 weeks ago
Hyderabad, India Novartis Full timeManage activities associated with the preparation of non-oncology Investigator Brochure (IB) annual updates within Biomedical Research (BR) in compliance with internal SOP and health authority requirements.Organizing and chairing the kick-off meeting to establish the level of update and contributors across Biomedical Research Translational Medicine and...
-
Submission Manager
1 month ago
hyderabad, India Novartis India Full timePosition Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) forNew Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental NDAs/BLAs/...
-
Submission Manager
1 month ago
hyderabad, India Novartis India Full timePosition Title : Submission Manager About The Role Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for New Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental...
-
▷ [Immediate Start] Submission Manager
6 days ago
Hyderabad, India Novartis India Full timePosition Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for- New Drug Applications (NDA), Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental NDAs/BLAs/...
-
Associate Editor
4 weeks ago
Hyderabad, India SciRes Literatire LLC Full time**Job Summary** - Associate Editor is responsible for communicating and building relationship with renowned scientists through mail and other modes of communication. **Responsibilities and Duties** - AE is responsible to follow the activities of the Editorial Board members and assist them in assigning reviewers for received submissions as on needed. -...
-
Senior Transparency Associate
4 weeks ago
hyderabad, India Novartis India Full timePosition Title :Senior Transparency AssociateAbout the role :Be part of a growing Industry expertise! Come, join a global team of nearly 200 regulatory professionals- life scientists, clinicians and project managers across 6 countries and support Novartis operational expertise in the mobilization of the organization’s commitment to sharing of clinical...
-
Senior Transparency Associate
4 weeks ago
Hyderabad, India Novartis India Full timePosition Title :Senior Transparency AssociateAbout the role :Be part of a growing Industry expertise! Come, join a global team of nearly 200 regulatory professionals- life scientists, clinicians and project managers across 6 countries and support Novartis operational expertise in the mobilization of the organization’s commitment to sharing of clinical...
-
Senior Transparency Associate
4 weeks ago
Hyderabad, India Novartis India Full timePosition Title : Senior Transparency Associate About the role : Be part of a growing Industry expertise! Come, join a global team of nearly 200 regulatory professionals- life scientists, clinicians and project managers across 6 countries and support Novartis operational expertise in the mobilization of the organization’s commitment to sharing of...
-
Regulatory Affairs Associate
3 weeks ago
Hyderabad, Telangana, India Parexel Full timeRegulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Contribute to preparation...
-
Regulatory Affairs Associate
3 weeks ago
Hyderabad, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for...
-
Regulatory Affairs Associate
1 week ago
hyderabad, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends,...
-
Clinical Research Associate
2 weeks ago
Hyderabad, India Learning Labb Research Institute Full timeAs a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:- Conduct site visits to monitor trial activities and ensure compliance...
-
Global Program Regulatory Manager- LCM
1 month ago
hyderabad, India Novartis Full timeYour responsibilities include but not are limited to:• Regulatory Strategy -Responsible for implementing regulatory strategy and managing operational activities for assigned regions.Provides input into global regulatory strategy and contributes to Regulatory Functional Plan (RFP) and Seed Document, or their equivalents, including identification of gaps or...
-
Sr. Associate
7 days ago
Hyderabad, Telangana, India Cognizant Technology Solutions Full timeTEAM LEADJob summaryWe are seeking a dedicated Team Lead - Senior Associate with a strong background in Field Services and a proven track record of leading teams to excellence. With a role that bridges technical expertise and team management the ideal candidate will drive operational efficiency ensure high-quality service delivery and foster a culture of...
-
Senior Regulatory Affairs Associate
4 weeks ago
Hyderabad, Telangana, India Parexel Full timeRegulatory Affairs LabelingBachelor's Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI, packaging)The...
-
Senior Regulatory Affairs Associate
1 month ago
Hyderabad, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Regulatory Affairs Labeling Bachelor’s Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling...
-
Senior Regulatory Affairs Associate
4 weeks ago
hyderabad, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Regulatory Affairs Labeling Bachelor’s Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling...
-
Project Manager
4 weeks ago
hyderabad, India Amogen Pharma Full timeThe ideal candidate should be able to a ssist in timely delivery of projects from start to finish by ensuring the execution as per master schedule and coordinating with various internal resources to ensure that the set timelines / milestones are met and escalation of deviations / lags in completion.Key Internal Stakeholders: R&D, Projects &...