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Centralized Monitoring Lead (R1055609) in Buenos Aires, Argentina at IQVIA™

Date Posted: 12/7/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Experience:
    Not Specified
  • Date Posted:
    12/7/2018
  • Job ID:
    R1055609

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.

PURPOSE

Provides leadership of the CMS team, in support of the project and clinical leader, and in collaboration with other functional teams, to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and practices.

RESPONSIBILITIES

  • Partners with the CL to perform oversight on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan (COP).
  • May perform functional lead responsibilities for assigned project deliverables for specific customers or projects/specified.
  • Should independently manage assigned global studies.
  • May attend study team and /or client meetings as needed or requested.
  • Contribute and/or oversee to the development and use of study management plans and/or DTE specific tools and templates and/or other study specific plans to evaluate the quality and integrity of the study.
  • Act as point of contact for assigned project deliverables.
  • May support project management team to develop monitoring strategy including monitoring triggers/thresholds.
  • Manage and monitor operational insight of the assigned project(s) and complete/oversee the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).
  • May contribute to developing the study specific analytics strategy and work on developing advanced analytics.
  • Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.
  • Identify the value adds from the medical review & remote monitoring in the study and provide the inputs to relevant stakeholders. Implement continuous improvement activities for assigned projects.
  • Manage project resources (CRAs/CMs/CTAs/CASs)
  • May perform and oversee the IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licences etc).
  • Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready.
  • May contribute in maintaining strong relationship with the stakeholders
  • May act as mentors or coaches for junior staff.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
  • Strong written and verbal communication skills including good command of English language.                                                                                                               
  • Results and detail-oriented approach to work delivery and output.                                                                 
  • Excellent motivational, influencing, negotiating and coaching skills
  • Ability to work on multiple projects and manage competing priorities.
  • Strong organizational, problem solving and decision making skills
  • Effective presentation skills.                                                                                                                                                   
  • Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.
  • To lead team and effectively work in team.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Bachelor's degree in life sciences or related field and min 4 years with relevant clinical research experience; or equivalent combination of education, training and experience
  • At least 4 or 5 years of relevant clinical monitoring experience
  • Advance English level (Mandatory)

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: R1055609