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:...

**Key Responsibilities**: - **Training Program Development**: - Develop and implement a robust training curriculum aligned with industry standards and regulatory requirements. - Create engaging training materials, including presentations, handouts, and online learning modules. - Design and deliver customized training programs to meet the specific needs of...

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

Reporting to: Assistant Manager – Regulatory Affairs Division: Ortho Implants Location: Chennai No. of Positions: 1 Education: B.E/ B. Tech in Biomedical Engineering / M. Pharm Regulatory Affairs Experience: 2 - 4 years Exp. in ‘scientific writing / clinical documentation’ role preferred KEY RESPONSIBILITIES: Technical writing, literature search,...

Dear Candidates, We have an opportunity with clinical trial development and CRO related assets and capabilities from an existing ACRO/SMO organization that is based in Chennai. We have over 10 years of experience running clinical trials as part of the global Group.  Position OverviewThe Head of Regulatory Affairs is responsible for providing strategic...

Responsibilities High clinical quality in the Company’s programs and improvement in outcomes of patients participating in the programs Serve as professional anchor for the registration as Clinical Establishment including liaison with patient’s doctors where needed Primary Execute ongoing oversight on patient reviews by Clinical Pharmacists to ensure...

**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 soundness...

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....

Summary 1 Conduct CME s seminars promotional events and In service programs in the respective region In order to improve BD SM value proposition amongst both clinical and economic buyers towards business outcome and achieve Regional business objectives 2 Clinical capability building amongst regional SM direct selling organisation and amongst channel partners...