GSS Pharma Pvt.LtdBengaluru Urban District
services to pharmaceutical companies worldwide.
Role Description
This is a full-time on-site role for a Drug Safety Associate at GSS Pharma Pvt.Ltd in Bangalore Urban. The Drug Safety Associate will be responsible for tasks related to Pharmacovigilance...
GSS Pharma Pvt.LtdBengaluru
This is a full-time on-site role for a Drug Safety Associate at GSS Pharma Pvt. The Drug Safety Associate will be responsible for tasks related to Pharmacovigilance, including assistance to QPPV, global literature monitoring, data entry and quality review, signal detection and evaluation, and prepar...
GSS Pharma Pvt.LtdBangalore
services to pharmaceutical companies worldwide.Role DescriptionThis is a full-time on-site role for a Drug Safety Associate at GSS Pharma Pvt.Ltd in Bangalore Urban. The Drug Safety Associate will be responsible for tasks related to Pharmacovigilance...
GSS Pharma Pvt.LtdBengaluru
Role DescriptionThis is a full-time on-site role for a Drug Safety Associate at GSS Pharma Pvt. The Drug Safety Associate will be responsible for tasks related to Pharmacovigilance, including assistance to QPPV, global literature monitoring, data entry and quality review, signal detection and evalua...
GSS Pharma Pvt.LtdBengaluru
Role DescriptionThis is a full-time on-site role for a Drug Safety Associate at GSS Pharma Pvt. The Drug Safety Associate will be responsible for tasks related to Pharmacovigilance, including assistance to QPPV, global literature monitoring, data entry and quality review, signal detection and evalua...
Get new jobs by email!
Get email updates for the latest Drug Safety Associate jobs in Bangalore
It's free, and you can cancel email updates at any time
Pharmacovigilance Services Associate
Accenture | Bangalore | www.accenture.com |
Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications:Any Graduation/Bachelor of Pharmacy/BSc. Nursing
Years of Experience:1 to 3 years
Language - Ability:Japanese - Intermediate
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.
Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions.
Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.
You will be a part of pharmacovigilance team helping with Japanese translations, triage and data entry of patient data into a safety database.
In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for? •Written and verbal communication
• Good listening skills
• Collaborate and work in a team
Certifications:
• JLPT Level 4
• The Japan Foundation and Japan Educational Exchanges and Services?; ABK-AOTS DOSOKAI
• JAPANESE LANGUAGE PROFICIENCY TEST – (JLPT)(Level 5
• N5); JLPT/Japanese Language Proficiency Test
• N3 - JEES
Roles and Responsibilities: •In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
• Your expected interactions are within your own team and direct supervisor
• You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
• The decisions that you make would impact your own work
• You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
• Please note that this role may require you to work in rotational shifts
Designation: Pharmacovigilance Services Associate
Qualifications:Any Graduation/Bachelor of Pharmacy/BSc. Nursing
Years of Experience:1 to 3 years
Language - Ability:Japanese - Intermediate
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.
Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions.
Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.
You will be a part of pharmacovigilance team helping with Japanese translations, triage and data entry of patient data into a safety database.
In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for? •Written and verbal communication
• Good listening skills
• Collaborate and work in a team
Certifications:
• JLPT Level 4
• The Japan Foundation and Japan Educational Exchanges and Services?; ABK-AOTS DOSOKAI
• JAPANESE LANGUAGE PROFICIENCY TEST – (JLPT)(Level 5
• N5); JLPT/Japanese Language Proficiency Test
• N3 - JEES
Roles and Responsibilities: •In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
• Your expected interactions are within your own team and direct supervisor
• You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
• The decisions that you make would impact your own work
• You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
• Please note that this role may require you to work in rotational shifts
Recommended jobs: