Remote Legal Specialist: Clinical Research Contracts

Indero; Buenos Aires; Remote; ARS 900,000 - 1,300,000; Full time

Benefits offered by this job

Flexible home-based position

Ongoing learning and development

Job summary

Indero is a contract research organization (CRO) focused on dermatology and Rheumatology, based in Montreal with international reach, now seeking a Legal Specialist to support the Legal Department in Argentina. The role covers contracts, governance, and regulatory compliance for clinical research activities.

You will prepare, review, and administer CTAs, CDAs, and vendor/consultant agreements; coordinate workflows and maintain contract databases; and assist with privacy and regulatory

Qualifications

• Diploma or certificate in Paralegal Studies or equivalent legal training.
• 3–5 years of paralegal or legal assistant experience, preferably in a CRO, pharmaceutical, biotech, or regulated environment.
• Strong understanding of contract administration and legal documentation.
• Excellent written and verbal communication in English.

Responsibilities

• Assist in the preparation, review, coordination, and administration of contracts related to clinical research activities, including CTAs, CDAs, vendor and consultant agreements, Amendments and addenda.
• Coordinate contract execution workflows, track signatures, versions, and approvals; maintain contract databases and document management systems.
• Support regulatory compliance activities for audits, inspections, and due diligence processes.
• Conduct legal and regulatory research related to healthcare, clinical research, data protection, and corporate law.

Skills

English communication

Organizational skills

Attention to detail

Prioritization

Education

Paralegal certificate or diploma

Equivalent legal training

Tools

Microsoft Office

Contract management systems

Job description

Indero is a contract research organization (CRO) focused on dermatology and Rheumatology, based in Montreal with international reach, now seeking a Legal Specialist to support the Legal Department in Argentina. The role covers contracts, governance, and regulatory compliance for clinical research activities.

You will prepare, review, and administer CTAs, CDAs, and vendor/consultant agreements; coordinate workflows and maintain contract databases; and assist with privacy and regulatory