Summary/Essential Duties & Responsibilities:
· Assume primary responsibility to collect details of adverse events received by phone or mail for ethicals and biologics and perform initial assessment according to local procedures and in accordance with company global drug safety procedures.
· Create initial reports by directly entering information into Drug Safety databases, amend reports and enter follow-up information as acquired, and prepare report for FDA submission.
Skills/Qualifications:
· Experience using database software/safety applications preferably S3 and/or Argus • Ability to independently identify problems and effectively offer solutions to problems
· Interpreting and applying medical information, instructions, policies and procedures and guidelines pertaining to drug safety
Education:
· Must have BS in health science field, Registered Nurse (RN), Pharm.D. Minimum of 1 year Pharmacovigilance (PV) experience
Contact: Hari
The best telephone number to reach me is 973-481-0100 Ext: 3051. I appreciate if you forward your updated word formatted resume at /narahari.pulikollumakroscientific.com for review before we speak.
For any reason, you are not able to submit your resume or for any further information, please call our Candidate Help Desk at 973-679-5005.or E-mail your resume at recruitermakrotech.com . We shall be happy to help you.
makroscientific.com for review before we speak.
