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Sr Consultant, Social Media (R1048324) in Warren, NJ at IQVIA™

Date Posted: 3/23/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Warren, NJ
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
    3/23/2019
  • Job ID:
    R1048324

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Sr Consultant, Tech                                                                                              Warren, NJ

Job responsibilities:

• Enable pharmacovigilance/adverse events (PV/AE) tracking business deals by supporting the onshore teams in the sales cycle, through building/enhancing suitable collaterals for the practice, including pitch decks, proposals, project plans, audit plans, and SOPs

• Liaise with the technology team to drive the PV/AE engagements successfully and leverage automation to enhance productivity as well as quality

• Use relevant medical experience in determining AEs of drugs/medicines for specific diseases/therapeutic areas

• Prepare the team for pharma company PV audits and to successfully undergo these audits

• Establish processes for training as well as certifications required for the PV practice

• Assist in other project management activities as required

• Responsible for creating training material relevant to PV/compliance practice

Qualification:

• 7+ years of experience in pharmacovigilance (post-marketing surveillance experience is highly necessary as opposed to AE tracking in clinical trials)

• Experience of driving the preparation for audits and successfully undergoing stringent audits by pharma companies as a PV agency/partner to a pharma company

• Knowledge of and exposure to unstructured data/social media data would be a plus

• High comfort level and affinity to using technology tools in the field of AE tracking

• Social adaptability – willingness to adapt to international cultures, work environments, and business processes

• Knowledge of processing/reporting requirements of ICSRs and thorough understanding of EU and US legislations on AE reporting

1. Essential: Sound safety knowledge of applicable good clinical practice (GCP), good pharmacovigilance practice (GVP), and International Conference of Harmonization (ICH) guidelines

2. Desirable: Related certifications/trainings such as client (pharma) AE certifications, DIA certifications, etc.

• Ability to establish and maintain effective working relationships with coworkers, managers, and customers

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled'

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™



Job ID: R1048324