1.0 - 5.0 years

0 Lacs

pune, maharashtra

On-site

As an individual responsible for assisting with Clinical Safety and/or PSS operations associated with products, your role will involve managing and processing expeditable adverse events, ensuring timely submission to clients and regulatory agencies if required. Your primary goal is to provide high-quality service to clients in a safe and cost-effective manner. It is essential for you to comply with legal requirements such as the Health and Safety at Work Act 1974, COSHH regulations 1989, and EC Directives 1992/3 as outlined in the Company's Health and Safety Manual. Key Responsibilities: - Assist in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) by maintaining ...

Posted 3 days ago

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Clinical Assistant / Senior Clinical Assistant / Clinical Associate / Senior Clinical Associate Kokilaben Dhirubhai Ambani Hospital

0.0 - 5.0 years

0 Lacs

maharashtra

On-site

You will be working in the Medical Staff department at Mumbai location with 0-5 years of work experience. As a Medical staff member, it is essential to maintain a professional approach towards patients, staff, and visitors. Your responsibilities include providing medical cover for routine and emergency cases, working collaboratively with other specialties, and following clinical safety and hygiene protocols. You must be willing and available to see patients as required and participate in classroom and bedside teaching programs for postgraduate students. Additionally, you will assist consultants in the operation theatre, perform surgeries under supervision, and handle complex surgical problem...

Posted 1 month ago

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Associate Director Biostatistics Novartis

6.0 - 10.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for providing highly advanced expert support and functional and technical leadership to ensure the scientific integrity and validity for clinical development, early development, and/or research projects. Your main tasks will include developing and applying biostatistics and programming methods to ensure valid conclusions, as well as providing statistical support for regulatory submissions, including planning, analysis, and reporting of clinical safety and efficacy summaries. Additionally, you may also provide statistical support to research or other R&D areas. To meet challenges in data review, big data, analytics, and reporting of clinical trial data, you may indepen...

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Associate Consultant / Senior Associate Consultant - ICU (Critical Care Medicine) Reliance Hospitals

0.0 - 5.0 years

0 Lacs

maharashtra

On-site

The Medical Staff position at our institute in Mumbai requires a professional approach in dealing with patients, staff, and visitors. You will be responsible for providing medical cover, both routine and emergency, and collaborating with other specialties. Your duties will include performing procedures such as Central line insertion, IV Channelization, Intubation, and operating instruments like Ventilator. Adherence to clinical safety, hygiene, and infection control protocols is essential, including wearing appropriate protective gear and maintaining hand hygiene. Monitoring patients as needed, identifying complex health issues, and promptly reporting to the concerned doctor are key responsi...

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Senior Pharmacovigilance Specialist Propharma Group India

4.0 - 6.0 years

7 - 9 Lacs

Hyderabad, Bengaluru

Hybrid

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 4 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pha...

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Pharmacovigilance Specialist Propharma Group India

2.0 - 4.0 years

4 - 5 Lacs

Hyderabad, Bengaluru

Hybrid

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 2 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pha...

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Spotfire Programmer : Life Science : 15 LPA : Apply Now Outpace Consulting Services

3.0 - 8.0 years

10 - 15 Lacs

Mumbai, Pune

Work from Office

Hi We are hiring for ITES Company for Spotfire Programmer Role. Responsibilities: Working on Refreshes requests for SRT & CSTV Building Oncology & Standard Visuals for Clinical Study Team Visualization (CSTV) Setting up standard and Study Specific requests for Safety Review Team (SRT) Knowledge of Spotfire, Study configuration tool and On Demand Tool. Creating SAS Codes as per the requirement Validation of visuals as per the specifications 1.5+ years of experience crafting interactive dashboards using TIBCO Spotfire. Adept at developing complex reports utilizing cross tables, bar charts, with advanced features like: property control, custom expressions, labels, and marking. Proficient in all...

Posted 3 months ago

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