ClinChoice Jobs in India

ClinChoice a partner to largest pharmaceutical innovators in world established 1995 provide expertise clinical operations biometrics regulatory affairs pharmacovigilance medical affairs toxicology help partners advance healthcare accelerating clinical trials data-driven insights ...

This is a role in the regulatory affairs department responsible for managing raw material data. The associate will handle requests from suppliers and stakeholders while maintaining high standards of technical understanding and data accuracy. · ...

The Senior Associate will collaborate with the client's regulatory project team to identify and collect necessary documents for EU MDR maintenance and resubmission. · ...

+End-to-end request governance for raw material data management involves timely initiation, adherence to turnaround time standards, handling supplier communication effectively, · and maintaining the Global Request Tracker. · On-time initiation within 24 hours of request receipt · ...

The Regional/Senior Artwork Controller is responsible for managing the end-to-end artwork development process from initiation through approval and release ensuring timely delivery of high-quality labeling components. · Manage the end-to-end artwork development process from initia ...

ClinChoice is seeking an Associate/Senior Associate for Regulatory Affairs (Drug Listing) to execute drug product lifecycle management activities and prepare regulatory submissions. · ...

Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems Interpret data analyze results using statistical techniques provide summary reports Develop implement databases data collection systems etc. · ...

ClinChoice is a partner to pharmaceutical innovators in the world. · Perform required data clean-up as per the defined process in RIMS. · ...

Collaborate with the client's regulatory project team to identify and collect documents in compliance with EU MDR. · ...

Handle inbound and outbound calls for Adverse Events (AEs), Product Complaints (PCs) and Medical Inquiries (MIs). Respond to web-based medical inquiries and product complaints received from Health Care Professional and consumers. · ...

Manage the preparation and submission of new product registrations. · Promote regulatory intelligence in both local and regional initiatives. · ...

The role involves collating data from primary/secondary sources or stakeholders and maintaining databases and data systems. · Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems · Interpret data, analyse results using statistic ...

Collaborate with the client's regulatory project team to identify and collect TF/DD documents in compliance with EU MDR and related guidance. · Work with cross-functional teams and affiliates to obtain necessary legal documents. Respond to inquiries from local affiliates and proa ...

ClinChoice is a partner to the largest pharmaceutical innovators in the world with expertise in clinical operations and regulatory affairs. · Actively collaborate with client's regulatory project team to identify TF/DD documents for EU MDR compliance · ...

ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. We provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, · and toxicology to help our partners advance healthc ...

ClinChoice es un socio de los innovadores farmacéuticos, dispositivos médicos y productos para el cuidado del consumidor más grandes del mundo. · ...

This role involves actively collaborating with the client s regulatory project team to identify and collect all necessary TF/DD documents in compliance with EU MDR (2017/745) and related guidance (MDCGs) · ...

+Job Title: · Senior Associate - Regulatory Affairs (Reg Ops EU MDR) · ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affair ...

This role involves end-to-end request governance for raw material data management. · ...

The Lead - Regulatory Affairs (EU MDR) will collaborate with the client's regulatory project team to identify and collect necessary documents for maintenance and resubmission according to EU MDR · Actively collaborate with the client's regulatory project team · Work with cross- ...