Senior Sap Mm Consultant - S/4Hana, Remote

Maxit Consulting - Max Corporate Group

Neuquén

Remote

ARS 182,877,000 - 274,315,000

Full time

14 days+

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Job summary

IQVIA is seeking a Centralized Monitoring Lead for LATAM to partner with the project and clinical leads to ensure delivery meets contract, SOPs and regulatory requirements, while optimizing speed, quality and cost of delivery.

This remote role spans LATAM sites and requires leadership of the monitoring team, coordination with global teams, and mentoring of junior staff to uphold study integrity and patient safety.

Qualifications

Bachelor's degree in life sciences.
+3 years of clinical monitoring experience with remote or on-site CRA responsibilities.
+2 years in a Lead role.
Advanced knowledge of ICH GCP and local regulations.
Strong English communication skills (mandatory).
Strong organizational and decision-making skills.
Results-driven with attention to detail.
Excellent motivational, influencing, negotiating and coaching skills.
Ability to manage multiple global projects with competing priorities.
Ability to lead and work effectively in a team.

Responsibilities

Oversee Centralized Monitoring team per protocol and SOPs.
Act as Unblinded Clinical Lead and manage IPs and study risk.
May lead the study or project close-out.
Manage project resources (CRAs, Central Monitors, CTAs).
Monitor study/site metrics and trend analysis; implement actions.
Contribute to analytics strategy and advanced analytics.
Support monitoring strategy with triggers/thresholds.
Attend study team and client meetings.
Provide inputs to study teams and drive continuous improvements.
Ensure documentation and eTMF readiness; audit readiness.
Mentor junior staff.

Skills

Lead role

English (Mandatory)

Project management

Communication skills

Team leadership

Problem solving

Regulatory knowledge

Multi-project mgmt

Education

Bachelor's degree in life sciences

Tools

eTMF systems

Job description

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

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)
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.

EEO Minorities/Females/Protected Veterans/Disabled

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Kelly is an equal opportunity employer committed to building a diverse, equitable, and inclusive workforce, including individuals of all races, genders, abilities, protected veteran status, sexual orientations, and gender identities. Equal Employment Opportunity is The Law.

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