Clinical Affairs

Age limit:20 to 30.Clinical Study Design & Execution: Leading the design and implementation of clinical study protocols and monitoring their progress.Regulatory Compliance: Ensuring all activities, from clinical trials to post-market evaluations, adhere to regulatory requirements and guidelines (e.g., FDA regulations, GCP).Data Management & Analysis:...

**Job highlights** - Years of Experience: Minimum 5 Years in Medical Device/ Pharma/ Life science. Qualification: M Sc Life Science/ BTech Medical / B Pharm/ M Pharm. - Minimum of 2-3 years of experience in regulatory affairs Healthcare industry, with specific experience in USFDA / 510K submission and MDSAP Audit preparation **Job description** This is a...

EXECUTIVE**: **Experience**: TWO TO FOUR YEARS**: **Positions**: 1**: **Location**: Chennai**: **Qualification**: P.HD in Clinical Research**:

Location - Chennai, Pune, Mumbai, Delhi , Noida, Indore, Jaipur, Vijayawada, Meerut, Surat Designation - Clinical Specialist Business Unit - Infusion Therapy / Vascular Access Report to - Head Medical Affairs Dotted line reporting to - State Head Poly Medicure Limited (Polymed, Listed in NSE: BSE), is a leading medical device manufacturer and exporter from...

**Key Responsibilities**: - **Regulatory Compliance**: Ensure compliance with ISO 13485, EU MDR 2017/745, US-FDA, CDSCO, and other applicable international standards for medical devices. - **Submissions and Approvals**: Prepare, review, and submit regulatory documentation, including 510(k) and IMDR submissions, to regulatory authorities such as US-FDA,...

- Provide scientific expertise, build knowledge and activity-based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer’s image in the scientific community.- To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical...

Position OverviewWe are seeking an experienced Clinical Data Specialist II to join our clinical research team in Chennai. The successful candidate will be responsible for accurate and timely data entry into Electronic Data Capture (EDC) systems from various e-source documents, including real-time data and Clinical Research Information Officer (CRIO) sources....

**Industry** Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position** Full Time, Permanent **Division** Pubrica Brand **Reports to**: Pubrica Business Head **About Company** Guires Group is a renowned global provider of services in advanced Contract Research, Data Science, Development, Pilot...

Location - Chennai, Pune, Mumbai, Delhi , Noida, Indore, Jaipur, Vijayawada, Meerut, Surat Designation - Clinical Specialist Business Unit - Infusion Therapy / Vascular Access Report to - Head Medical Affairs Dotted line reporting to - State Head Poly Medicure Limited (Polymed, Listed in NSE: BSE), is a leading medical device manufacturer and exporter...

Position OverviewWe are seeking an experienced Associate Manager - CDM to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration between...