Clinical & Regulatory Executive

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence- 20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager,...

The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial, and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator’s Study File...

Required skill set: #goodcommunicationskills #positiveattitude Experience: Minimum 6 month to 1 Year in DRA /Pharmaceutical Industry Job Location: Vikaspuri-Delhi Salary : Between 25K - 35K In Hand Education: Qualification in Pharmacy is preferable) - Having experience in dossier compilation (CTD ACTD) for CIS, ASEAN, LATAM and AFRICAN countries. -...

About the job Summary Monitors patient data study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely and accurate monitoring of patient data and...

Organisation :USV, a top -15 pharmaceutical company in India, excels in the diabetes and cardio sectors. With a presence in over 65 countries, our dynamic team of over 7,000 spans generations. Our commitment to brand building is evident in our popular products like Glycomet GP, Ecosprin AV, Jalra, Tazloc, Glynase and more.Responsibilities:For the CMC RA...

Job Description - **Regulatory Affairs Executive Medical Devices** As a Manager - Regulatory and Government Affairs for Medical Devices, you would be expected to actively engage with government stakeholders and regulatory bodies to ensure crisp and effective representation on regulatory and policy matters and ensure continuity of license and permits as well...

Job Title: Clinical Trials Data Strategist - AILocation: RemoteJob Type: Full-TimeAbout Us:At ngram, we are at the forefront of revolutionizing the clinical trial industry by integrating advanced artificial intelligence technologies into our solutions. Our platform is designed to enhance predictive analytics, streamline trial operations, and improve...

Clinical SAS Programmer (India)IndiaCRO - BiometricsFull-timeThe Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk...

**Responsibilities**: Regulatory Compliance: Stay up-to-date with the latest CDSCO India guidelines and other relevant regulations pertaining to medical devices. Ensure that all products and processes adhere to these guidelines. Regulatory Strategy: Develop and implement regulatory strategies for the successful approval and launch of medical devices in...

Looking for person having experience in European CE Certification - documentation of Medical Device & InVitro Diagnostics. Designation : Regulatory Affairs Executive Dealing with licensioing work with CDSCO, ICMR & other Govt institution Education : DPharma / MPharma / Btech for Pharma regulatory / Medical device Experiance : 2-5 Yrs Job location :...

Qualifications : B.Pharm/ M. Pharm/ M.Sc.Location: For two years in Brazil Office followed by Office in MumbaiJob descriptionResponsibilitiesEnsure change management, post approval changes to ANVISAReview of technical documents for new submissions, post approval changes (Individual Protocol, HMP).Writing PATE for post approval changesRespond to technical...

Job Title: Clinical Trials Data Strategist - AILocation: RemoteJob Type: Full-TimeAbout Us:At ngram, we are at the forefront of revolutionizing the clinical trial industry by integrating advanced artificial intelligence technologies into our solutions. Our platform is designed to enhance predictive analytics, streamline trial operations, and improve...

Organisation :USV, a top -15 pharmaceutical company in India, excels in the diabetes and cardio sectors. With a presence in over 65 countries, our dynamic team of over 7,000 spans generations. Our commitment to brand building is evident in our popular products like Glycomet GP, Ecosprin AV, Jalra, Tazloc, Glynase and more.Responsibilities:- For the CMC RA...

Senior / Labelling SpecialistJob Description:We are seeking a highly skilled and experienced Senior Labelling Specialist to join our team and take on a pivotal role in the development and approval of labelling documents for our vaccine portfolio. As a Senior Labeling Specialist, you will be responsible for overseeing all aspects of labeling, from initial...

Job Description:• Define solutions based on user needs by working with clinical science.• Create use cases and requirements.• Propose the overall feature design and evaluate between different design choices when available.• Interface to the Platform core-team for feature definition, interface definition with other subsystems.• Drive prototyping /...

Job DescriptionLocation: Mumbai, Chennai, Bangalore, Hyderabad, Ahemedabad,Delhi NCRAbout the Client:we have retained with CMMI level 4 client with the position of Banking operations for the level of SPE.Client is a global IT solutions company specializing in delivering simple and scalable solutions to address complexbusiness problems.More than 1,500 staff...

Design, create and test medical devices - Collaborate with quality assurance, engineering and regulatory professionals to assess the risks of medical devices - Collaborate with research, sales, marketing and communications professionals - Work with health departments,industry professionals and physicians to develop programs to improve health outcomes -...

1. To visit doctors, clinics, hospitals and other healthcare facilities in the neighborhood with a view to increasing the referrals to the clinic. 2. To conceive and implement effectively promotional activities aimed at retail/walk-in customers at housing societies, clubs, parks, shopping complexes or other, with camps, kiosking, road shows, branding...