ClinChoice Jobs in India

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

About ClinChoice · 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 affairs, pharmacovigilance, medical affairs, and toxicolog ...

The role of an Associate - Regulatory Affairs (RMQ) involves end-to-end request governance for raw material data management. The candidate should have technical expertise in regulatory requirements for raw materials within all categories of use. · ...

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. · ...

Job Title: Senior Associate -MICC · Employment Type: Full time · Location: Bangalore, India · Experience: 4+ Years · About Clinchoice · ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provi ...

· Job Title: Senior Associate -MICC · Employment Type: Full time · Location: Bangalore, India · Experience: 4+ Years · About Clinchoice · ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we pr ...

+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 ...

Handle inbound and outbound calls for Adverse Events (AEs), Product Complaints (PCs) and Medical Inquiries (MIs) and non-standard inquires. · ...

This role involves end-to-end request governance for raw material data management. · Initiate requests within 24 hours of receipt. · Adhere to turnaround times for all requests. · ...

Responsibilities: · Actively collaborate 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) for maintenance and resubmission. The high-level activities may include but a ...

Job Title: Specialist/Team Lead -MICC · Employment Type: Full time · Location: Bangalore, India · Experience: 4+ Years · About Clinchoice · ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we p ...

Collate data from primary/secondary data sources or stakeholders · and maintain databases and data systems. · ...

ClinChoice es un socio clave para los principales innovadores farmacéuticos, dispositivos médicos y productos de cuidado del mundo. · Se requiere experiencia en RIMS regulatory data management. · Se busca candidato con B.Pharm o M.Pharm. · ...

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. · ...

· About ClinChoice · 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 affairs, pharmacovigilance, medical affairs, and toxico ...

ClinChoice is seeking a Senior Associate to join its Regulatory Affairs team in Bengaluru, India. The successful candidate will be responsible for collaborating with clients' regulatory project teams, identifying and collecting necessary documents, and performing quality control ...

Primary Responsibilities: · Manage the preparation and submission of new product registrations, post approval submission and follow-up closely on queries and through approval. · Responsible for writing CMC modules 2 & 3. · Exposure to EU & CIS region in Regulatory filings · Manag ...

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 position involves collaborating with regulatory project teams to identify and collect necessary documents in compliance with EU MDR (2017/745) guidance. · Identify applicable regulatory requirements. · Create Adobe PDF files of TF/DD documents. · Upload bookmarks/indexes of ...

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 ...