DirecciónResponsibilities:
· Case triage, Quality Check, Related data entry, Other incidental clerical work and general affairs
· Ensure from onsite/offsite location a smooth execution of all Pharmacovigilance (PV) activities performed
· Provide guidance and supervision on process and delivery to the PV teams onsite
· Ensure that all client requests are completed on time, as per the deadline
· Clarify any confusion in Client updates when some information is unclear.
· Ensure a smooth communication between client and offshore team
Qualifications:
· Knowledge of pharmacovigilance (1 years or more, individual case triage or QC experience)
· Thorough expertise in processing pharmacovigilance activities (Quality control, ICSR management, specific reports)
· Knowledge of Pharmaceutical Affairs Law, GVP/GPSP Ministerial Ordinance and related operation
· Native level of Japanese and good knowledge of English language
Nice to have:
· Rigor and relationship skills
· Training experience for members
⇒Communication skills that are easy to understand and can convey things logically to others
· Experience handling for clients something
⇒the level of responding to client inquiries about cases
· Behavioral Competencies:
Good team management skill and communication skill. Strong learning ability.
Employee Status : Full Time Employee
Shift : Day Job
Travel : No
Job Posting : Feb 22 2024
About Cognizant
Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, age, or any other characteristic protected by law. If you have a disability that requires a reasonable accommodation to search for a job opening or submit an application, please email TAGJapan@cognizant.com with your request and contact information.
