Clinical Study Builder-Argentina
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| Company Name | Indero (formerly Innovaderm) |
| Company Type | Private |
| Job Type | Full-Time |
| Salary Range | Market Competitive |
| Location | Greater Buenos Aires |
| Qualifications | None / No Formal Education |
| Experience | 3 Year+ |
Job Overview
Indero (formerly Innovaderm) is seeking a Clinical Study Builder to join their team in Greater Buenos Aires, Argentina. This role is crucial for designing and configuring clinical studies, ensuring accurate data collection and compliance with protocols within Indero’s specialized dermatology and rheumatology CRO services.
Company Overview
At Indero, we specialize in providing comprehensive Contract Research Organization (CRO) services for dermatology and rheumatology. Our team feels like an extension of your own, offering scientific guidance, accurate results, and exceptional customer satisfaction.
Our Expertise: With over 25 years of deep medical and operational expertise in dermatology, we seamlessly translate our knowledge to rheumatology. We understand that dermatology and rheumatology are inextricably linked, as immune-mediated inflammatory skin and joint diseases often require similar treatments.
Our Services: We set the standard with our value-added services, including: Study Design and Protocol Development, Regulatory Submissions and Consulting, Trial Master Files Management, Project Management, Investigator/Site Selection, Patient Recruitment, Clinical and Medical Monitoring, Pharmacovigilance, Data Management and Biostatistical Analysis, Clinical Study Reports and Medical Writing.
Since 2000, Indero has built a strong reputation for the quality of our research and the care we offer to study participants, clients, and sites. We often exceed our clients’ timeline expectations, ensuring successful outcomes for every project.
Quick Details
- Salary Range: Market Competitive
- Job Type: Full-time
- Qualifications: none
- Experience: 3 Year+
Key Responsibilities
- Design and configure clinical study databases and electronic Case Report Forms (eCRFs).
- Develop and implement study build specifications based on approved protocols.
- Perform User Acceptance Testing (UAT) for all study builds to ensure data integrity and functionality.
- Collaborate with data management, clinical operations, and biostatistics teams.
- Ensure all study builds adhere to regulatory requirements and internal SOPs.
- Provide technical support and troubleshooting for ongoing clinical studies.
Requirements
- Proven experience in clinical study building, preferably within a CRO or pharmaceutical setting.
- Proficiency with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle InForm).
- Strong understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements.
- Excellent analytical skills and meticulous attention to detail.
- Ability to work effectively in a fast-paced and collaborative environment.
- Strong communication and problem-solving abilities.
Benefits
- Opportunity to work with a specialized CRO in dermatology and rheumatology.
- Engage in impactful work contributing to innovative clinical research.
- Professional development and career growth opportunities.
- Collaborative and supportive team environment.
- Competitive compensation and benefits package.
- Direct involvement in cutting-edge medical advancements.