Accenture hiring Freshers for Pharmacovigilance Services Associate – Apply Now

Pharmacovigilance Services Associate

LOCATION: CHENNAI  

JOB NO. AIOC-S01507699  

FULL-TIME

Job Description
Skill required: Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications: Bachelor of Dental Surgery/Bachelor of Pharmacy/Bachelor in Physiotherapy
Years of Experience: Fresher
Language – Ability: English – Expert

What are we looking for?

•Ability to perform under pressure •Agility for quick learning •Collaboration and interpersonal skills •Commitment to quality

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

Qualifications:
Bachelor of Dental Surgery,Bachelor of Pharmacy,Bachelor in Physiotherapy

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. Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases. 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.

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