Application Specialist Biomedical jobs
- ProPharma GroupIndia
- For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and…
- View all ProPharma Group jobs - India jobs - Specialist jobs in India
- Salary Search: Pharmacovigilance Specialist salaries in India
- Perfint Healthcare Pvt LtdDelhi, Delhi
- Translate imaging and procedural knowledge into application best practices.
- With a strong focus on innovation, Perfint develops advanced robotic and navigation…
- RemidioDelhi
- The Application Specialist – ROP Device is responsible for delivering effective product demonstrations to doctors and healthcare professionals, ensuring a clear…
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- Sunshine Manpower Solution And ServicesJaipur, Rajasthan
- Preventive & corrective maintenance of biomedical equipment.
- Troubleshooting and onsite service support.
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- MacgenceNoida, Uttar Pradesh
- In this role, you will play a critical part in the development of machine learning algorithms for medical imaging analysis and healthcare applications.
- 3B BlackBio Biotech IndiaBengaluru, Karnataka
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- B. BRAUN MEDICAL (INDIA)Hyderabad, Telangana
- Deliver technical training to hospital staff, including OT nurses and biomedical engineers, on the handling and care & maintenance of neuro surgical systems.
- B. BRAUN MEDICAL (INDIA)Hyderabad, Telangana
- Deliver technical training to hospital staff, including OT nurses and biomedical engineers, on the handling and care & maintenance of neuro surgical systems.
- Entrust Pro Medical SystemsBeltola, Guwahati, Assam
- - Experience:* Freshers and experienced candidates are welcome.
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- SiemensPune, Maharashtra
- 10+ years expertise as application engineer in simulation ; leveraging AI, data and data management, and simulation process orchestration as tools.
- Sir H. N. Reliance Foundation Hospital and...Mumbai, Maharashtra
- Requirement gathering with proper understanding and checking the feasibility with application.
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- MedtronicChennai, Tamil Nadu
- Prior experience in a clinical specialist, applications specialist, pre-sales support, or customer education role.
View similar jobs with this employerThermo Fisher ScientificBengaluru, Karnataka- At least 3 - 5 years of laboratory or commercial field applications experience.
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- Siemens HealthineersChennai, Tamil Nadu
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- ZEISS GroupBengaluru, Karnataka
- To support the planning, execution, and management of regulatory activities for global medical devices (software and hardware), ensuring compliance with EU MDR,…
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Job Post Details
Pharmacovigilance Specialist - job post
Job details
Job type
- Full-time
Location
Full job description
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Essential Functions:
- Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level.
- Perform case follow up activities such as identification of information to be collected during follow-up.
- Creating and reviewing case narratives.
- Providing client notifications as required for case management.
- Supporting and contributing to the development of training materials and training delivery.
- Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs.
- Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
- Peer reviews of cases for quality, consistency, and accuracy as needed.
- Other duties as assigned
Necessary Skills and Abilities:
- Strong verbal, written and interpersonal communication skills.
- High level of accuracy and attention to detail.
- Ability to identify and resolve problems in a timely manner.
- Able to work independently and collaboratively in a multi-disciplinary team.
- Excellent organization and prioritization skills; able to multitask.
- Basic knowledge of Pharmacovigilance.
Educational Requirements:
- Required: a Bachelor's degree in life sciences.
- Preferred: advanced degree, RN, RPh, PharmD or equivalent.
Experience Requirements:
Two years of related work experience.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***