Product Safety Specialist

100% Remote
Product Safety Specialist
Duration: 6 Months+
Shift: 1st Shift (EST Hours)
(Open for all over USA- But need some one who is ready to work in NJ-EST Zone)
Pay $40-48.57/hr on w2

Must Haves:
Safety reporting experience (AE/SAE, PSUR/ICSR, DSURs, PSURs/PBRERs) preferably in oncology and neurology.
Strong understanding of patient clinical information and a high attention to detail.
Ability to work in a fast-paced professional environment.

HM note:
Registered Pharmacists Degree & Licensure
Experience with processing Post-marketing and Solicited cases
Experience with collecting and performing follow-up by phone.
Strong verbal and written communication skills are essential.

Bachelors degree in medical field with RN or RPh licensure (Must Have), or PharmD/MD degree required.
Minimum 2 to 4 years in industry application of clinical medicine/pharmacy with a minimum of 1 year in pharmaceutical drug safety
Experience in verbally interviewing and/or providing medical information to health care professionals and consumers
Application of clinical medicine to patient care
Medical terminology and standards of patient care
Computer proficiency

Job Description:
Responsible for receipt and documentation of safety information for Marketed and Investigational Products. Interacts with health professionals and consumers to obtain and follow-up reports of possible adverse events with *** products.
Provides product information to health care professionals, consumers, and sales representatives. Codes and enters information into the global safety database. Verifies the accuracy, completeness and validity of information for each adverse event report for which he/she is responsible. Assures consistency of case records and documentation. Creates and ensures distribution of regulatory reports for FDA and other regulatory health authorities.

1. Accurate and timely data entry of both domestic and foreign adverse event and serious adverse event information into the PSSS (Product Safety Surveillance System) consistent with the ARISg coding manual, SOPs/WIDs, process flows and established time frames within the ARISg workflow. Full understanding of the products Company Core Data sheet, PI, and/or IB for accurate labeling and listedness. Perform appropriate and timely follow-up per department guidelines, including accurate and thorough communication documentation within the case. Maintain proficiency in the utilization of the PSSS, including MedDRA coding. This may include participating in the validation process for the PSSS. 65%

2. Ensure accurate and timely submissions to regulators, co-marketing partners and affiliates within company and regulatory timeframes. Utilize ARISg for all reporting and confirmation of successful distribution and acknowledgement. 15%

3. Maintain sufficient knowledge of all *** products to ensure professional and knowledgeable discussions with consumers and healthcare providers and dissemination of accurate product information in response to queries. Provide high level customer service to consumers, health care professionals and internal customers. 10%

4. Complete all required training within the timelines provided so as to ensure knowledge of all relevant corporate and departmental SOPs, SWPs and WIDs. 10%

Ensure timeliness in regulatory compliance.
Gather sufficient information to assess the medical significance of an adverse event report, while at the same time assuring the information provided adequately addresses the concerns of the health care provider and/or consumer.

Bachelors degree in medical field with RN or RPh licensure, or PharmD/MD degree required.
Minimum 2 to 4 years in industry application of clinical medicine/pharmacy with a minimum of 1 year in pharmaceutical drug safety.
Experience in verbally interviewing and/or providing medical information to health care professionals and consumers.
Application of clinical medicine to patient care.
Medical terminology and standards of patient care.
Computer proficiency.