Life Sciences at Syneos Health | Apply Now
Life sciences job opportunities in pharmacovigilance are rapidly expanding, and this role at Syneos Health offers a strong entry point into global drug safety. If you’re looking to build a career in PV, clinical safety, and regulatory compliance, this remote position in Mexico provides hands-on experience in ICSR processing, safety data management, and collaboration with global clinical teams.
- Job Position:Â Safety & PV Specialist I
- Location:Â Mexico (Remote)
About the Company
Life sciences job seekers exploring syneos careers will find that Syneos Health is a leading fully-integrated life sciences services organization focused on accelerating customer success. The company partners with innovators across drug development and commercialization, helping navigate complexity and deliver impactful healthcare solutions. With over 25,000 employees globally, Syneos Health contributes to a significant percentage of FDA-approved drugs and EMA-authorized products.
Job Description
Life sciences job involves supporting pharmacovigilance activities, including ICSR processing, safety data entry, and compliance with regulatory standards. The role requires collaboration with clinical teams and adherence to SOPs, GCP, ICH, and GVP guidelines while ensuring accurate safety reporting and documentation.
Qualifications
Life sciences job candidates applying for this job in Mexico opportunity should have:
- Bachelor’s Degree in life sciences or equivalent
- Knowledge of safety database systems and medical terminology
- Understanding of clinical trial phases (II-IV) and pharmacovigilance regulations (ICH GCP, GVP)
- Proficiency in Microsoft Office tools and communication platforms
- Strong organizational, analytical, and multitasking skills
- Excellent communication and interpersonal abilities
- Attention to detail with high accuracy and deadline management
Key Responsibilities
Life sciences job responsibilities include:
- Enter information into PVG quality and tracking systems for ICSR tracking
- Assist in processing ICSRs as per SOPs and safety plans
- Perform triage and evaluate ICSR data for completeness and accuracy
- Enter and code data in safety databases (MedDRA coding, drug dictionary maintenance)
- Compile narrative summaries and follow up on queries
- Ensure timely reporting of safety data as per regulatory requirements
- Maintain safety tracking activities
- Perform literature screening and safety review
- Handle duplicate ICSR identification and management
- Support SPOR / IDMP-related activities
- Conduct quality review of ICSRs
- Ensure proper documentation in Trial Master File (TMF)
- Participate in audits and maintain compliance with global regulations
