Pharmacovigilance Services New Associate
Pharmacovigilance Services New Associate
Posted on :
11-03-2025
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1 Vacancy
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Job Description
Job Title: Pharmacovigilance Services New Associate
Job Location: Bengaluru Karnataka India
Job Location Type: Onsite
Job Contract Type: Fulltime
Job Seniority Level: Entry level
Skill required: Pharmacovigilance Services Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services New Associate
Qualifications:Bachelor of Pharmacy
Years of Experience:0 to 1 years
Language Ability:English Advanced
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 699000 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
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 subofferings 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. Management of the Affiliate Mailbox reconciliation of reports per process and performance of all written followup attempts to include both Serious and Nonserious cases. In this role you will be expected to create and manage case identification data entry MedDRA coding case processing submission and followups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for
In this role you are required to solve routine problems largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined narrow scope of work Please note that this role may require you to work in rotational shifts Roles and Responsibilities: In this role you are required to solve routine problems largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined narrow scope of work Please note that this role may require you to work in rotational shifts
Bachelor of Pharmacy
Designation: Pharmacovigilance Services New Associate
Qualifications:Bachelor of Pharmacy
Years of Experience:0 to 1 years
Language Ability:English Advanced
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 699000 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
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 subofferings 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. Management of the Affiliate Mailbox reconciliation of reports per process and performance of all written followup attempts to include both Serious and Nonserious cases. In this role you will be expected to create and manage case identification data entry MedDRA coding case processing submission and followups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for
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Employment Type
Full Time
Key Skills
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