Clinical Data Coordinator (Argentina) Argentina · Permanent · Entry-level

Indero; Buenos Aires; Remote; ARS 1,000,000 - 1,400,000; Full time

Benefits offered by this job

Home-based position

Flexible work schedule

Ongoing learning and development

Job summary

Indero is seeking an entry-level Clinical Data Coordinator in Argentina to support data management across clinical trials. You will assist with data review, discrepancy management, and reporting while ensuring regulatory compliance and SOP adherence. A collaborative environment with learning opportunities is offered.

The role emphasizes accuracy, organization, and teamwork, with home-based work options and ongoing development opportunities within a CRO focused on dermatology and rheumatology.

Qualifications

• Education: B.Sc. or related field is required.
• Strong analytical capacity and data handling skills.
• Fluent English; French is a plus.

Responsibilities

• Provide general data management support to project team and vendors.
• Assist Lead Data Manager with data review, reconciliation, discrepancy management.
• Maintain study metrics and data status reports; generate ad-hoc reports.
• Assist in designing databases and creating data management plans.

Job description

## Clinical Data Coordinator (Argentina)Argentina · Permanent · Entry-level#### About The PositionThe Clinical Data Coordinator will participate in various clinical data management activities required to ensure that data captured in clinical trials undertaken, or managed by Indero, are collected, managed and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with applicable regulatory requirements, industry guidelines, and Indero standard operating procedures (SOPs) while respecting Indero’s commitment to sponsor’s requirements and timelines.**This role will be perfect for you if**:* You have strong analytical capacities and an ease to work with data.* You enjoy working with systems and technology, continuously learning.* You want to work in a collaborative team where your ideas are heard and valued.**RESPONSIBILITIES**-Provides general data management support to the project team, sponsor and external vendors, as needed.-Supports Lead Data Manager in the areas of:* Data Review.* Data Reconciliation.* Discrepancy Management.* Maintenance of Study Metrics; Monitoring study status (e.g. enrollment, CRFs monitored/approved, etc.) on an ongoing basis and provide data status reports to the project team, as needed.* Generation of Ad-Hoc Study Reports.* User Maintenance.* Assisting with User Acceptance Testing.* Assisting with designing of database.* Assisting with creating data management plan (DMP), and other clinical data management related documentation.* Assisting in ensuring that data management documentation is complete and up-to-date in the trial master file (TMF).#### Requirements**IDEAL PROFILE****Education*** B.Sc. or related field;**Experience*** 1 year of clinical data management experience in the pharmaceutical industry or in a CRO environment is considered an asset;* Experience using an EDC system (ie. Medidata Rave, Medrio) is considered an important asset.**Knowledge and skills*** Skilled in use of computer technology, and ability to learn new applications;* A general knowledge of CDASH/SDTM is considered an asset* Highly organized and detail-oriented with effective project planning and time management skills;* Strong verbal and written communication skills in English, French is an asset;* Ability to work in a fast-paced environment with demonstrated agility to juggle and prioritize multiple competing demands;* Excellent interpersonal, communication, problem solving and organizational skills with the ability to work both independently and in a team environment.* Understanding of the drug development process and of applicable regulations, including Good Clinical Practices, ICH Guidelines, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.#### Our company**The work environment**At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.In this position, you will be eligible for the following perks:* Flexible work schedule / work schedule :* Home-based position* Ongoing learning and development**About Indero**Indero is a contract research organization (CRO) specialized in dermatology and Rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.***Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.******Indero only accepts applicants who can legally work in Argentina***#### Apply for this position