Pharmacovigilance Services Associate<\/p>\n\n\n\n
Bachelor of Dental Surgery,Bachelor of Pharmacy,Bachelor in Physiotherapy<\/p>\n\n\n\n
Skill required:<\/strong> Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance End Date : 25th April, 2024<\/strong><\/p>\n\n\n\n
Designation:<\/strong> Pharmacovigilance Services Associate
Qualifications:<\/strong>Bachelor of Dental Surgery\/Bachelor of Pharmacy\/Bachelor in Physiotherapy
Years of Experience:<\/strong>Fresher
Language – Ability:<\/strong>English – Expert
About Accenture<\/strong>
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\u2014 all powered by the world\u2019s 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?<\/strong> 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\u00e2\u20ac\u2122s leading biopharma companies bring their vision to life \u00e2\u20ac\u201c 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.
What are we looking for?<\/strong> \u2022Ability to perform under pressure \u2022Agility for quick learning \u2022Collaboration and interpersonal skills \u2022Commitment to quality
Roles and Responsibilities:<\/strong> \u2022In this role you are required to solve routine problems, largely through precedent and referral to general guidelines \u2022 Your expected interactions are within your own team and direct supervisor \u2022 You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments \u2022 The decisions that you make would impact your own work \u2022 You will be an individual contributor as a part of a team, with a predetermined, focused scope of work \u2022 Please note that this role may require you to work in rotational shifts.<\/p>\n\n\n\n