Safety Surveillance Associate

DESCRIPTION:
Primary responsibilities include selecting and coding adverse events, suspect drugs, and concomitant medications; determining seriousness of AEs, writing/editing case narratives, performing labeling assessments, and requesting follow-up information. Candidates will be expected to develop and maintain expertise and knowledge of all assigned products within a given therapeutic area and adhere to applicable corporate and global regulations, guidelines, Standard Operating Procedures, data entry and writing practices.

QUALIFICATIONS:
HCP IS REQUIRED. Clinical experience and drug safety experience in the pharmaceutical industry is highly desired. Candidates must have demonstrated ability to prioritize and multi-task effectively while adhering to world-class standards of quality.

Candidates MUST be able to complete a one-year assignment. No travel required. All work to be performed on site in Bridgewater, NJ. Some OT required.

SKILLS
Quality Assurance, Quality Control

Synectics is an Equal Opportunity Employer.