Sr. Safety Associate, Pharmacovigilance
BioPhase Solutions 7 reviews - San Diego, CA

This job posting is no longer available on BioPhase Solutions. Find similar jobs:Senior Safety Associate jobs - BioPhase Solutions jobs

BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Sr. Safety Associate, Pharmacovigilance to work for a leading San Diego County biotechnology company.
Sr. Safety Associate, Pharmacovigilance

In this position, you will receive and analyze Serious Adverse Event (SAE) information for completeness, accuracy and regulatory reportability requirements; evaluate SAE case data with an emphasis on medical presentation, conduct discussions regarding specific patient case data with health care practitioners and Sponsors; determine regulatory reporting requirements based upon case data, product information, and FDA or ICH guidelines and regulations; prepare SAE Reports, including preparation of narrative summary; identify missing/discrepant data, write queries, address queries with site personnel, evaluate query responses, and resolve queries when complete. Additionally, you will maintain the SAE database and perform coding of adverse event terms and concomitant medications.

Required Skills

Advanced understanding of applicable FDA, GCP, and ICH guidelines

Working knowledge of pharmacovigilance and clinical safety regulations and guidelines

Experience with coding dictionaries (knowledge of MedDRA and WHO Drug coding)

Experience with drug safety databases

Experience working in a team environment within cross-functional teams and in a fast-paced environment

Demonstrates initiative in identifying and solving problems

Demonstrates strong interpersonal and communication skills, resourcefulness, and personal organization skills

Strong database management skills and computer application skills including Microsoft Office

Experience using safety database software/safety applications is preferred

Knowledge of medical terminology and standard medical practices, and the ability to digest and apply new knowledge regarding disease entities as related to specific clinical trials

Ability to communicate clearly and precisely, both orally and in writing; ability to research information and prepare detailed written documents with attention to detail

A keen interest in medicine, pharmaceuticals, and regulatory affairs is essential for maintaining quality performance for this position, and continuing education in these areas is encouraged

Required Experience

Qualified candidates will have a Bachelor's degree in nursing (B.S.N.), Registered Nurse (R.N.), or Doctor of Pharmacy and a minimum of 5-8 years relevant experience. Requires in-depth knowledge of medical terminology and of GCPs, ICH guidelines and FDA regulations with an emphasis on safety. Must possess a professional demeanor; demonstrate initiative, sense of urgency, ability to organize and prioritize, and keen attention to detail.

About this company
7 reviews