Clinical Research Manager (CRM)

MSD; Partido de Vicente López; Hybrid; ARS 154,971,000 - 216,960,000; Full time

Job summary

MSD is seeking a Clinical Research Manager in Argentina to lead the operational execution of assigned clinical studies from start-up to close-out. You will coordinate investigators, sites, CRAs, vendors, and cross-functional teams to ensure timelines, quality, and regulatory compliance across local and global studies.

The role requires a Bachelor's in Life Sciences, 6+ years in clinical research, and strong English communication in a global environment.

Qualifications

• Bachelor's degree in Life Sciences, Health Sciences, or related field.
• 6+ years in clinical research or equivalent.
• Experience as a Clinical Research Associate strongly preferred with monitoring experience.
• Oncology experience preferred.
• Advanced English proficiency for global cross-functional collaboration.

Responsibilities

• Lead operational execution of assigned clinical studies ensuring timelines, quality, and regulatory compliance.
• Coordinate investigators, sites, CRAs, vendors, and internal teams.
• Monitor study performance using dashboards, metrics, and data insights.
• Identify and mitigate risks related to regulatory, quality, and timelines.
• Support sites and teams with recruitment, site performance, and resource needs.
• Build relationships across local, regional, and global teams; influence stakeholders.
• Promote adoption of new processes, digital tools, and AI-enabled solutions.
• Contribute to continuous improvement in Clinical Operations.

Skills

Leadership

Project Management

GCP Knowledge

Stakeholder Management

Risk Assessment

Data-Driven Decision Making

Quality Management

Clinical Data Management

Education

Bachelor's degree in Life Sciences

Job description

The Clinical Research Manager (CRM) is responsible for ensuring the successful execution of assigned clinical studies at the country level, from study start-up through close-out. The CRM coordinates investigators, clinical research sites, vendors, Clinical Research Associates (CRAs), and internal cross-functional teams to ensure studies are delivered in accordance with agreed timelines, quality standards, study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This role serves as a key connection between local clinical operations and global study teams, proactively managing risks, resolving operational challenges, and driving effective study execution.

Key Responsibilities

Lead and oversee the operational execution of assigned clinical studies. Ensure study activities are delivered in accordance with timelines, quality expectations, protocols, GCP, and applicable local regulatory requirements. Coordinate and collaborate with investigators, research sites, CRAs, vendors, and internal study teams. Monitor study performance through clinical systems, dashboards, metrics, and data-driven insights. Proactively identify operational, regulatory, quality, financial, or timeline risks and implement appropriate mitigation plans. Exercise sound judgment and make decisions within the scope of assigned responsibilities, escalating issues when appropriate. Support sites and study teams in addressing operational challenges, including patient recruitment, site performance, resource constraints, compliance matters, and stakeholder alignment. Build strong relationships across local, regional, and global teams and effectively influence stakeholders without direct authority. Support the adoption of new processes, technologies, digital solutions, and evolving ways of working. Contribute to continuous improvement initiatives across Clinical Operations.

Required Qualifications

Required Qualifications: Bachelor's degree in Life Sciences, Health Sciences, or a related field. More than 6 years of relevant experience in clinical research. Previous experience as a Clinical Research Associate is strongly preferred, ideally including at least 3 years of clinical monitoring experience. Oncology Experience is preferred. Advanced English proficiency, with the ability to communicate effectively in a global and cross-functional environment. Strong knowledge of clinical research operations, Good Clinical Practice (GCP), and applicable local regulations. Demonstrated experience working effectively with investigators, clinical research sites, vendors, and cross-functional teams. Travel: 20%-30% locally & internationally. The ability to build trusted relationships, influence outcomes, negotiate effectively, and navigate complex stakeholder environments is critical to success in this role.

Required Skills

• Accountability
• Accountability
• Adaptability
• Change Management
• Clinical Data Management
• Clinical Research
• Clinical Research Management
• Clinical Site Management
• Clinical Trial Management
• Continuous Improvement Techniques
• Critical Thinking
• Customer Satisfaction Management
• Data-Driven Decision Making
• Decision Making
• Detail-Oriented
• Global Change Management
• Good Clinical Practice (GCP)
• Leadership
• Operational Activities
• Organizational Change Management
• Prioritization
• Problem Solving
• Project Management
• Quality Management
• Regulatory Submissions {+ 8 more}

Key Capabilities

Accountability & Decision Making

Takes ownership of outcomes for assigned clinical studies. Demonstrates autonomy and sound judgment within the scope of responsibility. Effectively determines when issues should be resolved independently and when escalation is required.

Digital & Data Proficiency

Effectively uses clinical systems, dashboards, performance metrics, and data to manage study execution. Leverages insights to anticipate risks, identify trends, and support informed decision-making. Demonstrates curiosity and openness toward automation, digital solutions, and company-approved AI-enabled tools.

Change Management

Actively contributes to and supports change initiatives. Facilitates adoption of new tools, processes, and ways of working. Supports colleagues and stakeholders in successfully navigating change.

Critical Thinking

Evaluates complex issues from multiple perspectives. Assess risks, implications, and trade‑offs before making decisions. Develops pragmatic solutions that balance operational, regulatory, quality, and business considerations.

Agile & Flexible Mindset

Adapts effectively to evolving study priorities and business needs. Operates successfully in dynamic, global, cross-functional, and virtual environments. Demonstrates resilience and flexibility when managing ambiguity or unexpected challenges.

Risk-based Decision Making & Leadership

Proactively identifies operational, regulatory, quality, financial, and timeline-related risks. Prioritizes actions based on potential impact to the study, patients, sites, and business. Applies a structured, risk-based approach to decision-making and problem-solving.

Relationship & Stakeholder Management

Builds strong and trusted relationships with investigators, clinical sites, vendors, and internal stakeholders. Influences effectively without relying on formal authority. Navigates complex negotiations, competing priorities, and conflict constructively. Demonstrates empathy, diplomacy, and strong written and verbal communication skills.

Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 11/11/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.