Pharmacovigilance Services Associate

0-2 years

Not Disclosed

Chennai

10 Nov. 11, 2024

Job Description

Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Services Associate

Location: [Insert Location]
Job Type: Full-Time

Company Overview:

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— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 employees 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.

Position Overview:

We are looking for a Pharmacovigilance Services Associate to join our Life Sciences R&D vertical. In this role, you will help drive pharmacovigilance and drug safety surveillance activities for our clients in the biopharma industry. You will be involved in the management of safety case reports, including identification, data entry, coding, case processing, and follow-ups as per global regulatory requirements.

This is an excellent opportunity for individuals with a background in pharmacy, physiotherapy, or nursing to gain valuable experience in the life sciences and pharmacovigilance field.

Key Responsibilities:

Case Management: Manage and process Individual Case Safety Reports (ICSRs) in the safety database, including case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for both serious and non-serious cases.
Safety Reporting: Perform written follow-up attempts for safety cases, ensuring compliance with client guidelines and global regulatory requirements.
Collaborate: Work closely with the Pharmacovigilance & Drug Safety teams to ensure timely and accurate reporting.
Documentation: Reconcile reports and manage the Affiliate Mailbox according to process requirements.
Compliance: Ensure that all activities are carried out in compliance with regulatory guidelines and internal standards.

What We Are Looking For:

Adaptability: Ability to perform under pressure, work well within a team, and adapt to changing priorities.
Quick Learning: Agility to quickly learn new processes and systems.
Problem-Solving: Ability to solve routine problems using established guidelines and precedents.
Teamwork: Willingness to collaborate within a team environment and work under the guidance of supervisors.
Shift Flexibility: This role may require working in rotational shifts.

Qualifications:

Education: Bachelor’s degree in Pharmacy, Physiotherapy, or Nursing.
Experience: 0 to 3 years of relevant experience in pharmacovigilance or a related field is preferred, but fresh graduates are also encouraged to apply.
Skills:
- Strong attention to detail.
- Good understanding of pharmacovigilance processes and regulations.
- Proficiency in data entry and case processing.

Additional Information:

Work Environment: Office-based with potential for shift work.
Career Development: As part of Accenture's Life Sciences R&D team, you’ll be part of a global company committed to your career growth and professional development.

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Pharmacovigilance Services Associate

Job Description

Job Title: Pharmacovigilance Services Associate

Company Overview:

Position Overview:

Key Responsibilities:

What We Are Looking For:

Qualifications:

Additional Information:

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