Hiring.Camp

Adverse Event SPOC

Weekday AI

ยท

Yesterday

Location
Bengaluru, Karnataka, India ยท Mumbai, Maharashtra, India
Workplace
Onsite
Type
Full-time
Department
Weekday's Client via platform
Experience
3+ years
Source
Workable

Description

๐—ง๐—ต๐—ถ๐˜€ ๐—ฟ๐—ผ๐—น๐—ฒ ๐—ถ๐˜€ ๐—ณ๐—ผ๐—ฟ ๐—ผ๐—ป๐—ฒ ๐—ผ๐—ณ ๐˜๐—ต๐—ฒ ๐—ช๐—ฒ๐—ฒ๐—ธ๐—ฑ๐—ฎ๐˜†'๐˜€ ๐—ฐ๐—น๐—ถ๐—ฒ๐—ป๐˜๐˜€

๐—ฆ๐—ฎ๐—น๐—ฎ๐—ฟ๐˜† ๐—ฟ๐—ฎ๐—ป๐—ด๐—ฒ: ๐—ฅ๐˜€ ๐Ÿฑ๐Ÿฌ๐Ÿฌ๐Ÿฌ๐Ÿฌ๐Ÿฌ - ๐—ฅ๐˜€ ๐Ÿด๐Ÿฌ๐Ÿฌ๐Ÿฌ๐Ÿฌ๐Ÿฌ (๐—ถ๐—ฒ ๐—œ๐—ก๐—ฅ ๐Ÿฑ-๐Ÿด ๐—Ÿ๐—ฃ๐—”)

Experience: 3+ yrs

Location: Bangalore, Mumbai

As a Adverse Event SPOC, you will serve as the primary point of contact for all adverse event (AE) matters within the organization, ensuring timely and accurate reporting to regulatory authorities and internal stakeholders. You will oversee the entire AE lifecycle, from initial signal detection through case processing and documentation, driving compliance with global pharmacovigilance regulations and internal SOPs. Your role will involve close collaboration with crossโ€‘functional teams, including clinical, medical, and regulatory to deliver highโ€‘quality safety data. You will also mentor junior staff, contribute to continuous improvement initiatives, and support audits and inspections with strong analytical and communication skills.

Skills

FDACompliance

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