
Submission Specialist
21 hours ago
JD:-
We have an exciting role of Submission Specialist (MLR+EMA) to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global clients, including many Fortune 50 companies.
About US
We are an integral part of Annalect Global and Omnicom Group, one of the largest media and advertising agency holding companies in the world. Omnicoms branded networks and numerous specialty firms provide advertising, strategic media planning and buying, digital and interactive marketing, direct and promotional marketing, public relations, and other specialty communications services. Our agency brands are consistently recognized as being among the worlds creative best.
Annalect India plays a key role for our group companies by providing stellar products and services in areas of Creative Services, Technology, Marketing Science (data & analytics), Market Research, Business Support Services, Media Services, Consulting & Advisory Services. We are growing rapidly and looking for talented professionals like you to be part of this journey. Let us build this, together
This is an exciting role and would entail you to
- Oversee the end-to-end submission process of materials to the MLR review platform (Veeva Vault Promo Mats)
- Understand and document client-mandated submission requirements and ensure these protocols are maintained with guidance from MLR/Submission managers
- Create, uphold, and maintain submission checklists for assigned brands and ensure accurate and timely MLR submissions into Client systems
- Maintain a comprehensive and accurate record of all current and upcoming submissions including the stage of review, job codes, references, and deadlines
- Annotate any notes/comments relevant to MLR reviewers onto the submission file (As required, for identifying derivative/pick-up content, or callouts for changes between reviews)
- Perform QC of MLR submission components/package prepared by the team, before submission, and prepare and submit electronic and/or paper MLR-submission, including electronic tagging and linking references in Client system
- Establish and build relationships with all internal cross-functional team members in collaboration with the Copy department, organize references to streamline project submissions
- Support cross-functional team with opening projects in Client review platforms in collaboration with the Editorial team
- Proofread/fact check against multiple source documents to confirm annotation accuracy
- Stay current with new electronic submission and regulatory documentation practices and standards
You will be working closely with
Our global medical communication agency teams. You will also be closely collaborating with our team of talented and designers to deliver high-quality services.
This may be the right role for you if you have
- 2-3 years of relevant work experience, preferably in science, medicine, or at a pharmaceutical advertising agency.
- Bachelors degree in science, specifically related to medicine or pharmaceuticals
- Demonstrated proficiency/mastery of English language
- Excellent written and oral communication skills
- Proficiency in Microsoft Office (Word, Outlook, Excel, PowerPoint) and Adobe Acrobat.
- Familiarity with Veeva Vault PromoMats and/or Fuse and PubMed
- Extremely detail-oriented and organized approach
- Ability to work collaboratively with multiple departments and levels within the agency
- Strong team-oriented approach and excellent interpersonal skills
- Ability to thrive and grow in a fast-paced environment
- Ability to prioritize deadlines and work under pressure.
- A passion for sciences and regulations
-
Submission Specialist
3 weeks ago
Bengaluru, India Annalect Full timeOverview: About Role: We have an exciting role of Submission Specialist (MLR+EMA)to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global clients, including many Fortune 50 companies. About Omnicom Global Solutions Omnicom Global Solutions (OGS)...
-
Submission Specialist
24 hours ago
Bengaluru, Karnataka, India Annalect Full time ₹ 9,00,000 - ₹ 12,00,000 per yearOverview:About Role:We have an exciting role of Submission Specialist (MLR+EMA)to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global clients, including many Fortune 50 companies.About Omnicom Global SolutionsOmnicom Global Solutions (OGS) is...
-
Submission Senior Specialist
3 weeks ago
Hyderabad, India Bristol Myers Squibb Full timeWorking with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...
-
Submission Senior Specialist
1 week ago
Hyderabad, Telangana, India Bristol Myers Squibb Full time ₹ 12,00,000 - ₹ 36,00,000 per yearWorking with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...
-
Submission Senior Specialist
1 week ago
Hyderabad, Telangana, India Bristol Myers Squibb Full time ₹ 20,00,000 - ₹ 25,00,000 per yearWorking with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...
-
Valuation Specialist
3 weeks ago
Gurugram, India GSPANN Full timeRole: Valuation Specialist Exp 5+ years Responsibilities: Review and update high volumes of investment valuation data• Identify and assess the client's submissions to achieve compliant results• Must process with efficiency and accuracy by using the proper methods/tools in accordance with company procedures • Maintain records of client submissions,...
-
Regulatory Affairs- eCTD Specialist
2 weeks ago
Hyderabad, Telangana, India Nooha Asp Full time ₹ 5,00,000 - ₹ 15,00,000 per yearRegulatory Affairs Hiring Profile eCTD SpecialistExperience Level: 3 to 6 YearsLocation: Work from office (Hyderabad)Skills & Qualifications:1.Education: Bachelor's or Masters degree in Life Sciences, Regulatory Affairs, or related field.2.Experience: 3 to 6 years of experience in regulatory affairs with a focus on eCTD submissions, preferably in the...
-
Invoicing Associate/Trainee
3 weeks ago
Bengaluru, India Nes Global Specialist Engineering Services Full timeInvoicing Associate Location: Bangalore "Join our growing team as an Invoicing Associate where accuracy counts ABOUT THE ROLE: As an Invoicing Associate, you will play a key role in maintaining the financial accuracy of our operations by ensuring timely and precise invoicing. You will be responsible for preparing and issuing invoices to customer and meet the...
-
Invoicing Associate/Trainee
2 weeks ago
Bengaluru, Karnataka, India Nes Global Specialist Engineering Services Full time ₹ 6,00,000 - ₹ 12,00,000 per yearInvoicing AssociateLocation: Bangalore"Join our growing team as an Invoicing Associate where accuracy countsABOUT THE ROLE:As an Invoicing Associate, you will play a key role in maintaining the financial accuracy of our operations by ensuring timely and precise invoicing. You will be responsible for preparing and issuing invoices to customer and meet the...
-
labeling specialist
2 weeks ago
Bengaluru, India Biocon Biologics Full timeRegulatory Affairs Labeling Specialist roleKey Responsibilities: Responsible for Creating Labeling Strategy for the health authority interactions and handling HA or Country Organization (CO) labeling queries for assigned program/ products. Ensure Artwork Management for Initial Submission / Commercial Launch activities in coordination with CFT team....