Associate Manager, Safety Operations Team

hace 1 semana

Ciudad de México, Ciudad de México IQVIA A tiempo completo
Job Overview

Essential Functions

  • Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
  • To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
- determining initial/update status of incoming events
- database entry
- coding AE and Products, writing narratives, Literature related activities, Quality review, assisting with reconciliation, case closure related activities, coordinating translations, as per internal/ project timelines. Creating, maintaining and tracking cases as applicable to the project plan.

  • Perform activities related to adjudication as applicable
  • Assess Safety data for reportability to relevant authorities, track reportable cases and report to regulatory authorities, ethics committees, institutional review boards, investigators, oversight groups per legislation, within timelines and in a format compatible to meet requirement as per project. Liaise with relevant stakeholders to facilitate expedited reporting.
  • Liaise with manager for regulatory tracking requirements and electronic reporting.
  • Contribute knowledge and expertise to or lead assigned deliverables in the field of Safety Publishing, Risk Management, Safety Surveillance and Medical Information or other service lines as appropriate.
  • Ensure to meet quality, productivity and delivery standards per project requirements.
  • Ensure compliance to all project related processes and activities.
  • Build a positive, collaborative team environment with Safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff, assist Operations Manager as a backup when needed.
  • Provide and impart technical and process information to Safety Management and members of operational team on project specific issues.
  • Provide oversight role and have a good understanding of operational team on status, metrics, productivity and initiatives.
  • Maintain a thorough understanding of project protocol, therapeutic indication, budget and scope of work (SOW) for assigned projects
- set up and maintain project files, standard templates, electronic forms, databases and workflow as per project requirement.

  • Establish and maintain effective team and project service operations communications i.e. provide regular feedback to operations team manager and other relevant stakeholders on project metrics, out of scope work challenges/issues and successes
- effective feedback on project performance to junior members of team.

  • Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring completeness of individual training plan and maintain up to date training transcripts.
  • Participate or Lead trainings across Safety process service offerings
- participate in working groups as applicable in implementation of new initiatives, identification and implementation of process efficiencies.

  • To demonstrate problem solving capabilities.
  • Liaise with different functional team members, e.g. project management, clinical, data management
- health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.

  • Attend project team meetings and provide regular feedback/ inputs to Operations team manager on operational project metrics, out of scope work challenges/issues and successes.
  • To liaise with client in relation to details on day to day activities as needed.
  • Contribute to achievement of departmental goals
  • Perform other duties as assigned
  • 100% compliance towards all people practices and processes
  • In addition to the above mentioned responsibilities, depending on the project requirement, the team member may perform medical review of nonserious adverse events (AEs) and nonserious adverse drug reactions (ADRs) which includes reviewal of AE coding, past medical history, concomitant medications, expectedness/ listedness, causality assessment and other medical information and ensure completeness and accuracy of data according to applicable regulations and guidelines, SOPs, projectspecific guidelines, and medical evaluation guidelines and communicate with the team leads for any correction required in the case and maintain appropriate documentation for all communications.

Qualifications:

  • Bachelor's Degree Scientific or healthcare discipline or allied life sciences Req
  • Bachelor's degree in life sciences or related field and up to 5 years of relevant experience, inclusive of up to 3 years of Pharmacovigilance experience. Req
- or equivalent combination of education, training and experience. Pref

  • Excellent knowledge of medical terminology. Intermediate
  • In depth knowledge and understanding of applicable global, regiona

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