Trainee - Regulatory Operations (Rims)

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

JOB DETAIL RR 2 : RIMS (Regulatory Information Management Systems ) Technical Support • Total 5 Yrs of experience in Regulatory Applications and eSubmisisons, out of which a mandatory minimum 2-3 Yrs Experience in Veeva RIMS (Regulatory Information Management Systems) Technical/Product Application Support.Ability to carry our L2/ L3 technical Support •...

**_Regulatory Affairs Associate _**: **Experience: RIM**: **Relevant experience in Regulatory and should be willing to work in EU Shifts (12:00 - 9.00 PM)**: - **Experience of handling RIM tools - Veeva Vault specifically.**: - **Basic Regulatory knowledge on regulations and Health Authorities.**: - **Excellent communication skills.** **Knowledge and...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Regulatory Professional I - Clinical trial Submission **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department**:EU Submissions Hub- Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure...

Role Summary:Corporate Records and Information Management (CRIM) ProgramMonitor CRIM Program based on policies / guidelines, ensuring compliance with applicable regulatory, legal, and governmental compliance.Provide guidance and monitor the CRIM program throughout the organization.Perform internal audits and record inventories on hardcopy and electronic...

Role Summary:Corporate Records and Information Management (CRIM) ProgramMonitor CRIM Program based on policies / guidelines, ensuring compliance with applicable regulatory, legal, and governmental compliance.Provide guidance and monitor the CRIM program throughout the organization.Perform internal audits and record inventories on hardcopy and electronic...

**Trainee**: **Take your next career step at ABB with a global team that is energizing the transformation of society and industry to achieve a more productive, sustainable future. At ABB, we have the clear goal of driving diversity and inclusion across all dimensions: gender, LGBTQ+, abilities, ethnicity and generations. Together, we are embarking on a...

**JOB DESCRIPTION** Are you looking for an exciting opportunity to join a dynamic and growing team in a fast paced and challenging area? This is a unique opportunity for you to work in the Regulatory Operations team to partner with the Business. As a Regulatory Operations - Regulatory Reporting - Associate within the Regulatory Operations CoE, you will...

**Department: Global Regulatory Affairs - GBS - EU Submission Hub** **About the Department** Global Regulatory Affairs (GRA) in Global Business Services (GBS) Bangalore is a global RA hub consisting of high calibre regulatory professionals. The objective of the team is to offer core RA competencies enabling NN secure fast, high quality product approvals....

**Department: Global Regulatory Affairs - GBS - EU Submission Hub** **About the Department** Global Regulatory Affairs (GRA) in Global Business Services (GBS) Bangalore is a global RA hub consisting of high calibre regulatory professionals. The objective of the team is to offer core RA competencies enabling NN secure fast, high quality product approvals....

The position As Regulatory Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: Working closely with various submission teams across the organization and all countries in Europe Managing initial clinical trial application...

Department: EU Submissions Hub Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to...

**OPERATIONS** Operations is a dynamic, multi-faceted function that partners with all areas of the firm to deliver banking, sales and trading and asset management capabilities to clients around the world. Alongside this vital service delivery role, Operations provides essential risk management and control, preserving and enhancing the firm’s assets and...

**This is a Non IT Role** **Job Title: Trainee Recruiter (Night Shift)** **Location: Whitefield, Bengaluru, India (Onsite, No Remote or Work From Home)** **About Us**: - Creatigrity is a leading recruitment firm specializing in Human resources. We pride ourselves on delivering high-quality talent solutions to our clients while providing a supportive and...

Are you looking for an exciting opportunity to join a dynamic and growing team in a fast paced and challenging area? This is a unique opportunity for you to work in the Regulatory Operations team to partner with the Business.As a Regulatory Operations - Regulatory Reporting - Associate within the Regulatory Operations CoE, you will cater to private clients...

Bengaluru- Big team (20+ people)- ClientDataArt is a global software engineering firm. With over 25 years of experience, teams of highly-trained engineers around the world, deep industry sector knowledge, and ongoing technology research, we help clients create custom software that improves their operations and opens new markets. We invite to the company, not...

We are seeking highly skilled and experienced DGCA (Directorate General of Civil Aviation)-approved remote pilot trainers to join our team. As a Remote Pilot Trainer, you will be responsible for providing comprehensive training and instruction to aspiring drone pilots, ensuring compliance with DGCA regulations and industry best practices. Your expertise will...

**Job Description: Clinical Research Trainee** **Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments,...

Regulatory Professional I - Labelling **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN- .**Department**:RA Labelling Projects & Planning- **The position** - As a Regulatory Professional I - Labelling at Novo Nordisk, you will be responsible for the following: - Packaging Material Coordination: Collaborate with...