Remote Bilingual Legal Case Manager (Part-Time)

Ceo Lawyer Personal Injury Law Firm; Quilmes; Remote; ARS 1,200,000 - 2,600,000; Full time

Job summary

IQVIA is seeking an Associate Project Lead in Buenos Aires to manage integrated study plans, vendor relationships, and cross-functional collaboration. You will oversee portions of clinical studies, drive efficiency, and help ensure quality and cost control within contracts.

The role emphasizes English communication, data-driven decision making, and proactive risk management across geographies, with opportunities to advance within the project leadership ladder.

Qualifications

• Bachelor's Degree in life sciences or related field required.
• 4–5 years of clinical research experience, majority in project management in a CRO or pharma company.
• Strong vendor management experience is mandatory.
• Excellent English written and verbal communication with strong presentation skills.
• Robust problem solving, organization, time management, and cross-collaboration abilities.
• Ability to work across geographies and understand cultural differences.
• Sound understanding of project finances.

Responsibilities

• Provide input to develop integrated study management plans with the core project team.
• Serve as primary contact for vendors for project/vendor management activities.
• Be accountable for assigned portion of studies, optimizing speed, quality and cost.
• Set sub-team objectives and communicate performance expectations.
• Collaborate with other functional groups to achieve milestones and resolve issues.
• Monitor progress against contract and present information to stakeholders.
• Identify risks and contingencies and support issue resolution.
• May serve as primary or backup project contact with customers.
• Lead sub-team efforts for milestone achievements and cross-collaboration.
• Support the project leader in ensuring financial success and revenue acceleration.
• Identify scope changes and manage change control with the project leader.
• Capture lessons learned and implement best practices.

Skills

Vendor management

English communication

Problem solving

Organization

Cross-collaboration

Financial understanding

Communication skills

Presentation skills

Education

Bachelor's Degree in life sciences or related field

Job description

Buenos Aires, Argentina

Full time

Job Overview

Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The Associate Project Lead support the efforts of CPM to drive operational excellence and strategic leadership with our customers. Associate Project Leads may run their own studies, as part of their development.

Essential Function

• Provide input in to the development of integrated study management plans with the core project team and/or sub-team.
• Will be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.
• Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
• May serve as primary (for small projects) or back-up project contact with customer.
• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
• Support the project leader in ensuring the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
• Identify changes in scope and partner with project leader to manage change control process as necessary.
• Identify lessons learned and implement best practices.

Qualifications

• Bachelor's Degree In life sciences or related field required.
• +4-5 years of clinical research experience, being the majority of those years in a project management capacity in a CRO or pharma company.
• Strong vendor management experience is mandatory.
• Communication - Strong written and verbal communication skills including good command of English language . Strong presentation skills.
• Problem solving - Strong problem solving skills.
• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
• Finances - Good understanding of project financials.

IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification.

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.

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