Supervisor De Campo – Perforación (Remoto, Turnos 14X14)

Boart Longyear Ltd.; Ciudad de Mendoza; Remoto; ARS 137.587.000 - 198.737.000; Tempo pieno

Descrizione del lavoro

Boart Longyear Ltd. is seeking a Centralized Monitoring Lead for LATAM with remote work flexibility. You will lead the Centralized Monitoring team, ensuring delivery of clinical deliverables per protocol, SOPs and sponsor expectations across global projects.

Responsibilities include managing study metrics, developing analytics strategies, supporting risk mitigation, and mentoring junior staff, while coordinating with project teams and client meetings to optimize speed, quality and cost.

Competenze

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience.
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced command of English (Mandatory).
• Strong organizational, problem solving and decision making skills.

Mansioni

• Lead Centralized Monitoring team and oversee clinical deliverables per protocol, SOPs and project plans.
• Act as Unblinded Clinical Lead with IP management and regulatory duties as needed.
• Manage project resources (CRAs, Central Monitors, Clinical Trial Assistants).
• Monitor and analyze study/site metrics, develop analytics strategies and monitor RBM tools.
• Attend study team and client meetings and provide input to key decision makers.
• Ensure complete documentation and eTMF oversight; support process improvements.
• Mentor or coach junior staff.

Conoscenze

Clinical monitoring

Team leadership

English proficiency

Communication skills

Project coordination

Formazione

Bachelor's degree in life sciences or related field

Descrizione del lavoro

Centralized Monitoring Lead in LATAM (Remote)

Buenos Aires, Argentina
Mexico City, Mexico
Santiago, Chile
Lima, Peru
São Paulo, Brazil
Bogota, Colombia
Full time
R

Job Overview

The Leader of the Centralized Monitoring team, partner with the project and clinical lead 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 IQVIA SOPs, policies and practices.

Essential Functions

• Leadership activities:
  • Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical deliverables on global assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.
  • Unblinded Clinical Lead, including IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.)
  • May act as Clinical Lead when there is not assigned to the study and at project close out.
  • Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants)
• Analytical activities:
  • Manage, monitor and complete 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 compliance etc.).
  • Contribute to developing the study specific analytics strategy and work on developing advanced analytics.
  • Support project management team to develop monitoring strategy, including monitoring triggers/thresholds.
  • Attend study team and /or client meetings.
  • Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.
  • Development and use of study management plans, and/or RBM specific tools and templates, and/or other study specific plans to evaluate the quality and integrity of the study.
  • Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready, including eTMF oversight.
  • Mentors or coaches for junior staff.

Qualifications

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (as remote or on site CRA). 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.
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced command of English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Results and detail-oriented approach to work delivery and output.
• Excellent motivational, influencing, negotiating and coaching skills.
• Ability to work on multiple global projects and manage competing priorities.
• To lead team and effectively work in team.

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