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Junior Micc Associate

1-3 years years
3 LPA to 5 LPA
10 July 17, 2024
Job Description
Job Type: Full Time Education: BSC, MSC, B Pharma, M Pharma, Pharma D 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 Opening: Junior MICC Associate

 

Job Description

We are currently seeking a Junior MICC Associate to join our growing team within the Medical Information Contact Centre (MICC) for the Pharmacovigilance function.

Location: Banglore

 

Key Responsibilities

  • Follow global and local regulations to protect personal and client-related data as per company policy.

  • Responsible for receiving calls/emails (AE, PQC, MI & GI), case intake, duplicate check, and registration.

  • Follow up inquiries through phone or email, including translation if not in English.

  • Exhibit detail-oriented etiquette and a friendly attitude when answering telephone calls.

  • Appropriately escalate calls to the supervisor when necessary.

  • Ensure timely completion of internal/external training as assigned.

  • Participate in audits and ensure timely closure of CAPAs.

  • Provide support in other MICC-related activities as per business requirements.

Individual Case Safety Report Responsibilities

  • Data entry of individual case safety reports (all case report types) into the safety database.

  • Review and evaluate AE case information to determine required action based on internal policies and procedures.

  • Process cases to meet timelines with defined quality and productivity to meet project SLAs and KPIs.

  • Code all medical history, events, drugs/procedures/indications, and laboratory tests according to the appropriate dictionary (e.g., MedDRA, Company Product Dictionary, WHO-DD).

  • Write and/or check the correctness and completeness of medically relevant safety narratives in chronological order.

  • Ensure the completeness and accuracy of data entered in various fields.

  • Prepare and archive source documents as required.

  • Perform necessary changes in demoted/back-routed cases from Quality Reviewer/Medical Reviewer.

  • Review QR feedback and address feedback comments if necessary.

  • Coordinate with other workflows as required.

  • Act as a Subject Matter Expert for assigned projects, providing review feedback, mentoring, and training to enhance 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 communication and coordination.