Manager-Biologics Regulatory Affairs(Clinical Trials)

About USV Private Limited:USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries.Function: BiologicsPosition: Asst Manager / Manager - Regulatory Affairs (Clinical Trials) For EU and US.Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday...

About USV Private Limited:USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors and has presence in over 65 countries.Function: BiologicsPosition: Asst Manager / Manager - Regulatory Affairs (Clinical Trials) For EU and US.Job Location: Govandi (East ), Mumbai (1st, 3rd, 5th Saturday working, 2nd and 4th Saturday...

You will be working as an Asst Manager / Manager in the Biologics function of USV Private Limited in the Regulatory Affairs department specifically focusing on Clinical Trials for the EU and US markets. Your role will involve the following key responsibilities: - Developing Biosimilar Clinical Development Strategy, focusing on clinical trials and injectables...

Job DescriptionPosition: Sr. Executive/Asst. Manager/Deputy Manager-Regulatory Affairs (Domestic).Location: Andheri, Mumbai.Qualification: M. Pharm. (Experienced preferred).JOB DESCRIPTION Regulatory Affairs (Domestic)The role will involve expertise in D & C Act and Rules as well as FSSAI regulations withexperience in FDA related activities. This profile...

Designation: Asst Manager/Manager – Medicoregulatory AffairsDepartment: Medicoregulatory AffairsJob location :Kandivali-West, MumbaiResponsibilitiesI To independently review following applications online through Sugam Portal to CDSCO:Import license of reference product for BE studiesBE study NOC for export purposeManufacture of new drugs to be introduced...

Job Responsibilitiesminimum 2 Years of project management experience.Should have global pharma experience.Candidate from Mumbai location preferred.Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executedImplement clinical research protocols and ensure compliance with regulatory...

Clinical Research Associate RoleWe are seeking a highly motivated and experienced Clinical Research Associate to join our team. In this role, you will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and facilitating site-level documentation.

Job OpportunityWe are seeking a highly skilled Site Contract Manager. This role will be responsible for managing contracts and agreements with clinical trial sites, ensuring compliance with regulatory requirements.Key ResponsibilitiesPrepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and/or...

Job Title: Clinical Quality Assurance Compliance & training Experience : 5 plus years Location: Mumbai Type: Full-time Experience Level: (Senior) Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality...

Cliniminds is hiring Senior Associate Regulatory Affairs on behalf of globsl consulting company.Role Summary:The Senior Regulatory Associate plays a key role in supporting regulatory submission activities across Asian markets, primarily for biosimilar products. This role involves hands-on drafting, quality checking (QC), and performing Level 1 review of eCTD...