SrCRA1 - FSP | Argentina

IQVIA; Buenos Aires; On-site; ARS 138,361,000 - 184,482,000; Full time

Job summary

IQVIA is seeking a Senior CRA to plan, execute, and manage clinical trials. The role focuses on data integrity, regulatory compliance, and trial success across multiple projects. You will monitor sites, support recruitment planning, and ensure protocol training.

The position requires strong communication and the ability to work independently and with teams in a fast-paced environment. Ideal candidates have a health-care or scientific background, 4+ years of on-site monitoring experience, and

Qualifications

• Bachelor's degree in a health care or scientific discipline or equivalent.
• Minimum 4 years of on-site monitoring experience.
• Proficiency in GCP and ICH guidelines and regulatory requirements.
• Strong organizational and time management abilities.
• Excellent verbal and written communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Experience with CTMS and EDC systems.
• Willingness to travel as required.

Responsibilities

• Perform site initiation, monitoring and close-out visits with documentation.
• Support development of a subject recruitment plan.
• Train sites on protocol and study procedures and provide ongoing study training.
• Evaluate site practices for quality; escalate issues as appropriate.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with colleagues across functions and external customers.

Skills

GCP & ICH knowledge

Advanced in English

Organizational & time management

Communication & interpersonal skills

Independent and team collaboration

Willingness to travel

Education

Bachelor's degree in health care or related field

Tools

CTMS

EDC systems

Job description

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.

While projects vary, your typical responsibilities might include:

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

REQUIREMENTS

You should have:

• A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
• At least 4 years of on-site monitoring experience.
• Advanced in English.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Strong organizational and time management skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel as required.

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 https://jobs.iqvia.com

IQVIA 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.