FAQs
What qualifications are required for the Pharmacovigilance Services Associate position?
The required qualifications are a Bachelor of Pharmacy, a Bachelor in Physiotherapy, or a BSc in Nursing.
How many years of experience are needed for this role?
The role is open to candidates with 0 to 3 years of experience.
What industry does this position work within?
This position is aligned with the Life Sciences R&D vertical.
What are the main responsibilities of a Pharmacovigilance Services Associate?
The main responsibilities include managing the Affiliate Mailbox, reconciling reports, performing written follow-ups, managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database according to client guidelines and applicable global regulatory requirements.
Will I be required to work in shifts?
Yes, this role may require you to work in rotational shifts.
What skills are essential for this position?
The essential skills include adaptability, agility for quick learning, commitment to quality, and the ability to perform under pressure.
Who will I be interacting with in this role?
You will primarily interact with your own team and your direct supervisor.
Will I have the opportunity for further training and instructions?
Yes, you will receive detailed to moderate levels of instruction on daily tasks and detailed instruction on new assignments.
Is previous pharmacovigilance experience required for this role?
Previous pharmacovigilance experience is not required, as the position is open to candidates with up to 3 years of experience.
What is the main focus of the work in this role?
The main focus of the work is to support the world's leading biopharma companies in improving outcomes by connecting scientific expertise with insights into the patient experience.