Kickstart Your Career in Pharmacovigilance with Accenture: Exciting Opportunities Await!
The pharmaceutical industry is evolving rapidly, and with it, the demand for skilled professionals in pharmacovigilance and drug safety surveillance is growing. If you’re looking for an exciting career in this field, Accenture has an incredible opportunity for you as a Pharmacovigilance Services Associate.
Why Choose a Career in Pharmacovigilance?
Pharmacovigilance plays a crucial role in ensuring drug safety, monitoring adverse effects, and maintaining regulatory compliance. As a professional in this field, you contribute directly to patient safety and healthcare advancements. Whether you are a recent graduate or an experienced candidate, a role in pharmacovigilance offers a stable and rewarding career path.
About Accenture
Accenture is a global leader in digital transformation, cloud computing, security, and consulting. With a presence in over 120 countries and a workforce of 699,000 professionals, Accenture empowers industries with innovative solutions. Life Sciences R&D is one of its key verticals, offering services in research laboratories, clinical trials, regulatory affairs, and pharmacovigilance. Joining Accenture means working alongside top-tier experts, leveraging technology, and contributing to groundbreaking healthcare solutions.
Pharmacovigilance Services Associate – Job Details
Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications: BSc, Bachelor of Pharmacy, or Bachelor of Physiotherapy
Experience: 1 to 3 years
What Will You Do in This Role?
As a Pharmacovigilance Services Associate, you will be responsible for:
✔ Managing case identification, data entry, and MedDRA coding
✔ Processing and submitting Individual Case Safety Reports (ICSRs)
✔ Ensuring compliance with global regulatory requirements
✔ Handling the Affiliate Mailbox and reconciling reports as per protocols
✔ Performing follow-ups for both serious and non-serious adverse events
✔ Working with biopharma companies to enhance patient safety and drug monitoring
This role will immerse you in a fast-paced environment where accuracy and regulatory knowledge are essential. Your expertise will help pharmaceutical companies meet safety standards and improve patient experiences.
Who is the Ideal Candidate?
If you possess the following qualities, this role could be the perfect fit for you:
✔ Agility for Quick Learning – Ability to adapt to new regulations and industry changes
✔ Adaptable and Flexible – Willingness to work in a dynamic setting
✔ Team Player – Ability to collaborate with colleagues and supervisors effectively
Roles & Responsibilities:
🔹 Solve routine problems using existing guidelines and protocols
🔹 Work closely with team members and supervisors
🔹 Follow detailed instructions for daily tasks and new assignments
🔹 Make decisions that impact your work while following established procedures
🔹 Contribute as an individual team member within a structured scope
🔹 Be open to rotational shifts as per project requirements
Why Join Accenture?
✅ Global Exposure – Work with international pharmaceutical leaders
✅ Career Growth – Build expertise in pharmacovigilance with industry-leading professionals
✅ Technology-Driven Environment – Utilize AI-driven solutions for enhanced drug safety monitoring
✅ Competitive Benefits – Enjoy attractive remuneration and perks
Take the Next Step in Your Career!
If you’re passionate about drug safety and looking to grow in the pharmaceutical sector, this is your chance to make a difference. Apply now to join Accenture’s pharmacovigilance team and contribute to global healthcare advancements.