FAQs
What qualifications are required for the Pharmacovigilance Services Associate position?
The required qualifications for this position are a Bachelor of Pharmacy or a Master of Pharmacy.
How many years of experience do I need for this role?
You need 1 to 3 years of experience in pharmacovigilance or drug safety surveillance.
What is the work environment like for this position?
The work environment involves being part of a team within the Life Sciences R&D vertical, with a focus on pharmacovigilance and regulatory services.
What are the main responsibilities of a Pharmacovigilance Services Associate?
The main responsibilities include managing the Affiliate Mailbox, reconciling reports, processing cases, data entry, MedDRA coding, and ensuring compliance with client guidelines and global regulatory requirements.
Will I receive training for this position?
Yes, you will receive detailed to moderate levels of instruction on daily tasks and detailed instructions for new assignments.
Is this position a team-based role?
Yes, you will be an individual contributor as part of a team with a focused scope of work.
Are there shifts involved in this role?
Yes, this role may require you to work in rotational shifts.
What types of problems will I be solving in this role?
You will be required to solve routine problems largely through precedent and referral to general guidelines.
Who will I be interacting with in this position?
Your expected interactions will primarily be within your own team and with your direct supervisor.
Where can I find more information about Accenture?
More information about Accenture can be found on their website at www.accenture.com.