Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Junior Micc Associate

Navitas Life Sciences
Navitas Life Sciences
1-3 years
Not Disclosed
10 Sept. 27, 2024
Job Description
Job Type: Full Time 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 Description

We are seeking a Junior MICC Associate to join our expanding team.

As part of the Medical Information Contact Centre (MICC) within the Pharmacovigilance function, your responsibilities will include:

  • Adhering to both global and local regulations to protect personal and client-related data in line with company policies.
  • Managing the intake of calls and emails (AE, PQC, MI & GI), including case registration and duplicate checks.
  • Following up on inquiries via phone and email, providing translations when necessary (if the inquiry is not in English).
  • Maintaining a detail-oriented and friendly demeanor while handling calls.
  • Escalating calls to supervisors when needed.
  • Completing internal and external training as assigned in a timely manner.
  • Participating in audits and ensuring timely closure of CAPAs.
  • Supporting various MICC-related activities based on business needs.

Key Responsibilities:

  • Individual Case Safety Reports:
    • Enter individual case safety reports into the safety database.
    • Review and evaluate adverse event case information to determine required actions following internal policies and procedures.
    • Process cases to meet established timelines, quality standards, and productivity goals in line with project SLAs and KPIs.
    • Code medical history, events, drugs/procedures/indications, and laboratory tests using appropriate dictionaries (e.g., MedDRA, Company Product Dictionary, WHO-DD).
    • Write and verify the accuracy and completeness of medically relevant safety narratives in chronological order.
    • Ensure completeness and accuracy of data entered across various fields.
    • Prepare and archive source documents as needed.
    • Implement necessary changes based on feedback from quality and medical reviewers.
    • Review and address feedback received from quality reviewers.
    • Coordinate with other workflows as required.
    • Act as a Subject Matter Expert for assigned projects, providing review feedback, mentoring, and training to enhance team quality.

Desirable Skills and Experience:

  • 1-3 years of experience in an MICC role.
  • Graduate or postgraduate degree in life sciences.
  • Strong communication skills for effective client interaction and coordination.