Drug Safety Specialist at Precision Medicine Group

Mexico, chihuahua, Mexico -

Full Time

Start Date

Immediate

Expiry Date

16 Jun, 26

Salary

0.0

Posted On

18 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

ICSR Processing, SOPs, Safety Plans, Data Entry, Argus Safety Database, MedDRA, WHODrug, Case Narratives, Query Resolution, Regulatory Reporting, Database Reconciliation, TMF, PV System MF, GCP, ICH, GVP

Industry

Pharmaceutical Manufacturing

Description

We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring a Safety Specialist to join our growing team! The Safety Specialist is an integral part of the safety team and performs all aspects of the collection, processing, and reporting of individual case safety reports (ICSR) for clinical trials and/or post‑marketing programs. Main Duties & Responsibilities: Process ICSRs according to SOPs and project-specific safety plans Triages ICSRs, evaluates data for completeness and regulatory reportability Enter data into Argus Safety Database Code events, medical history, concomitant meds, and tests Draft case narratives Query resolution and follow‑up until complete Generate timely expedited regulatory reports Coordinate reconciliation of safety and clinical databases Ensure required safety reports distribution Participate in audits/inspections Submit documents to TMF/PV System MF Maintain compliance with SOPs, GCP, ICH, GVP, regulations Attend department meetings Participate in project meetings Other duties as assigned Education and Experience: Minimum Education & Experience: Minimum 2 years clinical trial drug safety experience; Bachelor’s degree in Pharmacy, Nursing, Life Science, or equivalent. Experience with Argus Safety Database, MedDRA, WHODrug, FDA/EMA/ICH safety regulations Professional working proficiency in English Preferred Education & Experience: Early phase oncology experience preferred Knowledge, Skills, and Competencies: Strong knowledge of safety reporting requirements and guidelines Ability to analyze and evaluate clinical safety data Strong written communication and narrative writing skills Experience with Argus, MedDRA, WHODrug Strong attention to detail Ability to manage multiple cases and deadlines Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Responsibilities

The Safety Specialist is responsible for all aspects of collecting, processing, and reporting individual case safety reports (ICSR) for clinical trials and/or post-marketing programs. Key duties include processing ICSRs according to SOPs, entering data into the Argus Safety Database, coding events, and generating timely expedited regulatory reports.