Job Responsibilities:
Under supervision, evaluate literature reports for potential cases of adverse events or safety concerns requiring further investigation and escalate case processing and follow-up.
Extract pertinent safety data from identified literature sources, including adverse events, safety signals, and other relevant information, ensuring accuracy and completeness.
Enter relevant safety data into pharmacovigilance databases or tracking systems, maintaining clear and organized documentation of literature screening activities and outcomes.
Stay updated on pharmacovigilance regulations, guidelines, and best practices related to literature screening and pharmacovigilance signal detection and incorporate new knowledge into daily activities.
Minimum Qualifications:
Bachelor's degree or equivalent in Pharmacy, Life Sciences, Nursing, or related field
1 Year of Relevant Experience
Job Category Summary:
Pharmacovigilance literature screening involves the systematic review of scientific and medical publications to detect adverse drug reactions and ensure drug safety. Professionals in this field critically assess research articles, clinical trial data, and other relevant literature to identify potential safety signals and maintain regulatory compliance.
At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.