Clinical data Spec- Coordinator
On-site · San Jose, Provincia de San José, Republic of Costa Rica
Job Summary
Clinical Data Specialist – Coordinator role based in Costa Rica. You will support the acquisition, review, and integration of external clinical trial data, coordinate with internal teams and vendors, perform data quality checks, contribute to study deliverables, participate in study-related activities, prioritize tasks, manage timelines, and escalate issues as needed across multiple studies and therapeutic areas. Candidates should have a Bachelor’s degree (or equivalent experience), ~1+ year in clinical research or drug development, understanding of clinical trials and data quality, familiarity with CDISC standards (CDISC, SDTM, ADaM), strong attention to detail, solid communication and collaboration skills, and proficient use of Microsoft Office. Must be based in Costa Rica and willing to work in Costa Rica. EEO & accommodations information provided; ongoing global collaboration with cross-functional and international teams.
Required Qualifications
- Bachelor’s degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)
- Approximately 1+ year of experience in clinical research or drug development
- Basic understanding of clinical trials, ICH-GCP, and data quality principles
- Familiarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM)
- Strong attention to detail and problem-solving skills
- Effective communication and collaboration abilities
- Ability to manage multiple priorities in a dynamic environment
- Proficiency in Microsoft Office tools
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