Pharmacovigilance and Patient Safety Associate
Job Description: • Process and manage serious adverse events • Oversee study patients’ safety matters • Work closely with other departments, sponsors, and investigator sites • Ensure proper plans are in place to appropriately collect and report Adverse Events (reputed company) and Serious Adverse Events (SAEs) • Facilitate the development and implementation of training programs for internal and external personnel managing safety information • Assist the department head in managing relevant safety group activities Requirements: • Bachelor’s Degree in a science or related field required • 2-4 years of pharmacovigilance and/or drug safety experience in a CRO, pharmaceutical, or clinical trial environment required • Proficient with International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines • Knowledge of medical terminology, clinical trials, and clinical research • Excellent project management, written and oral communication, organizational, and interpersonal skills • Familiarity with and ability to effectively utilize safety databases • Proficiency in English (written and verbal) required • Ability to build and lead effective project teams, motivate others, delegate, and make and implement decisions • Ability to build and maintain trust and confidence and communicate effectively with clients, external vendors, and internal team members • Ability to mentor and delegate Benefits: • Remote working • Flexible time off • Paid holidays • Medical insurance • Tuition reimbursement • Retirement plans • Applicable bonus Apply tot his job Apply To this Job
