IQVIA Walk In Interview 2022.IQVIA Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.Innovative emerging biopharma and biotech companies are driving the drug development pipeline; competition for funding and resources is fierce. IQVIA delivers flexible clinical development solutions designed for the specific needs of biotech companies.
- Post Name: Safety Aggregate Reporting Specialist
- Educational Qualification : 15 years of full time education. (Prefer B.Pharama, M.Pharma, Pharm.D, BDS, MDS, BAMS & BHMS graduates) ,or Equivalent Degree is desired.
- Experienced: 4 to 8 Years
Job Description: Greeting from IQVIA Ltd !!!!
Important Details :
- Post of date:22/11/2022
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Professional Attributes : 1) Good communication skills 2) Excellent analytical skills 3) Team player (As per business mandate and role)
Roles and Responsibilities
Act as Signal Management Lead on post-marketing and clinical trial projects. Set-up, implement, organize (including documentation) and lead safety management teams. Set-up and update products’ signaling strategies. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks . Responsible for full documentation and tracking of signals.
In a PV support role, lead/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.
Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory affairs Reporting (RR), Real World Late Phase (RWLP), Medical Writing, Clinical Research, Quality, Knowledge Quality Management (KQM), Pharmacovigilance Support (PVS), Project Leads (PL), Medical Safety Advisors (MSA), Qualified Persons for Pharmacovigilance (QPPV) / Pharmacovigilance Contact at National Level (PCNL), Library Information Services (LIS), Safety Operations (SO), and Information Technology (IT), as needed.
Participate in internal and external audits and inspections, as required.
Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented.
Serve as the interface between the global project lead and the working team
conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.
Note:– Candidates who are interested can please revert with your updated resume to raviranjankumar.Singh@iqvia.com.